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Insulin-like growth factor 1 receptor

The insulin-like growth factor 1 receptor (IGF1R) is a transmembrane receptor tyrosine kinase that plays a central role in mediating the biological effects of insulin-like growth factors (IGFs), particularly IGF-1 and IGF-2, by binding them with high affinity and activating downstream signaling pathways essential for cell growth, proliferation, differentiation, survival, and metabolism.^[1] Encoded by the IGF1R gene on human chromosome 15q26.3, it forms a heterotetrameric structure consisting of two extracellular α-subunits responsible for ligand binding and two transmembrane β-subunits containing the intracellular tyrosine kinase domain.^[2] Expressed ubiquitously from the oocyte stage through adulthood, with notably high levels in tissues such as the kidney and ovary, IGF1R is critical for embryonic development and postnatal growth, as evidenced by severe growth retardation and developmental defects in mice with disrupted Igf1r genes.^[1]^[2] Upon ligand binding, IGF1R undergoes dimerization and autophosphorylation of its β-subunits, triggering multiple intracellular signaling cascades, including the phosphatidylinositol 3-kinase (PI3K)/AKT pathway for anti-apoptotic and metabolic effects, the RAS/mitogen-activated protein kinase (MAPK)/extracellular signal-regulated kinase (ERK) pathway for proliferation and differentiation, and the Janus kinase (JAK)/signal transducer and activator of transcription (STAT) pathway.^[2] IGF1R can also form hybrid receptors with the insulin receptor (INSR), which bind IGFs and insulin with altered affinities, further modulating signaling outputs in tissues like muscle and fat.^[2] In some contexts, activated IGF1R translocates to the nucleus, where it influences gene transcription independently of cytoplasmic pathways.^[2] These mechanisms underscore IGF1R's role in maintaining homeostasis, as its knockout in animal models leads to intrauterine growth restriction and perinatal lethality.^[2] Dysregulation of IGF1R, most commonly through overexpression or hyperactivation, is strongly associated with oncogenesis and tumor progression in multiple malignancies, including breast, prostate, lung, and colorectal cancers, where it promotes cell survival, metastasis, and resistance to chemotherapy by suppressing apoptosis.^[2] Germline mutations in IGF1R cause rare growth disorders such as Desbuquois dysplasia type 2 and severe intrauterine growth retardation due to IGF-1 resistance, highlighting its non-redundant function in linear growth.^[1] Therapeutically, IGF1R has been targeted with monoclonal antibodies (e.g., figitumumab, ganitumab) and small-molecule tyrosine kinase inhibitors in clinical trials, showing promise in combination regimens for advanced solid tumors despite challenges like pathway crosstalk and feedback activation.^[2]

Structure

Subunit Composition and Assembly

The insulin-like growth factor 1 receptor (IGF1R) is a heterotetrameric transmembrane receptor tyrosine kinase composed of two extracellular α-subunits linked by disulfide bonds and two β-subunits that span the plasma membrane.^[3]^[4] The α-subunits are entirely extracellular and primarily responsible for ligand recognition, while the β-subunits contain the intracellular tyrosine kinase domains essential for signal transduction.^[4] IGF1R is synthesized as a single-chain 1367-amino acid precursor pro-receptor, which undergoes post-translational processing including signal peptide removal and glycosylation in the endoplasmic reticulum.^[4]^[5] Furin-mediated proteolytic cleavage at a specific site (between residues 740 and 741 of the precursor) generates the mature α-subunit (approximately 710 residues, encompassing residues 31-740 of the precursor) and β-subunit (approximately 627 residues, residues 741-1367).^[3]^[4] This cleavage occurs after glycosylation and is necessary for the receptor to achieve its functional configuration.^[4] The functional receptor assembles into an α₂β₂ heterotetramer through a combination of disulfide bridges and non-covalent interactions, with intra-monomer disulfides linking each α to its paired β-subunit and inter-monomer disulfides connecting the two α-subunits.^[6]^[3] This assembly begins with dimerization of the pro-receptor monomers in the endoplasmic reticulum, followed by cleavage and maturation in the Golgi, ensuring proper ligand binding and kinase activation.^[4] The heterotetrameric structure is critical for high-affinity ligand interaction and downstream signaling.^[6] Structural studies of the IGF1R ectodomain, such as the crystal structure of its first three domains (PDB entry 1IGR), reveal a modular architecture that contributes to the overall V-shaped conformation of the assembled ectodomain in higher-resolution models.^[7] This V-shaped arrangement positions the ligand-binding sites at the apex, facilitating dimerization and activation upon ligand engagement.^[7]

Domain Organization and Ligand Binding

The insulin-like growth factor 1 receptor (IGF1R) is a transmembrane tyrosine kinase composed of distinct domains that contribute to its structural integrity and function. The extracellular region, spanning approximately the first 900 residues, is organized into several modules: two leucine-rich repeat domains (L1 and L2), a cysteine-rich region (CR), and three fibronectin type III domains (FnIII-1, FnIII-2, and FnIII-3). The L1 domain (residues 1–150) forms a compact β-helix structure with leucine-rich repeats that participates in ligand recognition, while the L2 domain (residues 300–460) adopts a similar fold but plays a lesser direct role in binding. The CR (residues 152–298) consists of 11 disulfide-linked modules stabilized by 22 cysteine residues, bridging L1 and L2 and contributing critically to the receptor's ligand specificity. The FnIII domains (residues 461–901) facilitate interdomain interactions and include the site for proteolytic cleavage into α- and β-subunits, with FnIII-2 containing an insert domain.^[4]^[7] The transmembrane domain (residues 906–929) comprises a single α-helical span that anchors the receptor in the plasma membrane and supports preformed dimerization essential for its activity. Intracellularly, the β-subunit features a juxtamembrane region, a tyrosine kinase domain (TK; residues 973–1229), and a C-terminal tail. The TK domain exhibits a bilobal architecture typical of receptor tyrosine kinases, with an activation loop containing key tyrosine residues (Y1161, Y1165, and Y1166) that undergo autophosphorylation to regulate kinase activity. The C-terminal tail (beyond residue 1229) includes additional autophosphorylation sites, such as Y1250 and Y1251, which serve as docking platforms for downstream effectors.^[4]^[8]^[9] Ligand binding occurs primarily through the extracellular α-subunits, with high-affinity interaction sites formed by the L1, CR, and L2 domains of one protomer in conjunction with the α-C-terminal segment and FnIII-1 of the opposing protomer. IGF-1 binds with high affinity (Kd ≈ 0.1 nM), engaging residues in the L1-CR groove and inducing structural rearrangements that separate the β-subunits. IGF-2 exhibits lower affinity (approximately 10–50-fold reduced compared to IGF-1), while insulin binds with even lower affinity (about 100-fold less than IGF-1), underscoring the receptor's specificity despite sequence homology among the ligands. These binding events rely on the dimeric assembly of the receptor, with the CR and L1 domains providing the primary contacts for ligand specificity.^[7]^[10]^[3]

Receptor Family

Insulin Receptor Superfamily

The insulin-like growth factor 1 receptor (IGF1R) is a receptor tyrosine kinase (RTK) that belongs to the insulin receptor (IR) superfamily, a distinct group within the broader RTK family characterized by their unique preformed dimeric architecture.^[11] Encoded by the IGF1R gene located on chromosome 15q26.3 in humans, IGF1R shares this classification with other members due to its role in transducing signals for growth and metabolic regulation through tyrosine kinase activity.^[1] This superfamily is often grouped under RTK class II, emphasizing their evolutionary divergence from other RTK classes that typically dimerize only upon ligand binding.^[12] The core members of the IR superfamily include the insulin receptor (IR), encoded by the INSR gene on chromosome 19p13.2; IGF1R itself; and the insulin receptor-related receptor (IRR), which has more restricted expression and an unidentified physiological ligand.^[11] Additionally, hybrid receptors form through heterodimerization between these members, such as IR/IGF1R hybrids, which combine α and β subunits from different receptors and exhibit altered ligand affinities that influence both metabolic and mitogenic signaling.^[13] These hybrids are prevalent in tissues where both IR and IGF1R are co-expressed, contributing to the superfamily's functional versatility.^[14] The IR superfamily arose from ancient gene duplications during early vertebrate evolution, approximately 500 million years ago, coinciding with the two rounds of whole-genome duplication (2R hypothesis) at the base of vertebrates. A primary duplication event generated the ancestral IR lineage, followed by a secondary duplication that separated the progenitors of IGF1R and IRR, leading to their diversification while preserving high sequence conservation. For instance, IGF1R shares over 50% overall sequence identity with IR, rising to 84-85% in the intracellular tyrosine kinase domain, reflecting their common evolutionary origin.^[15] All superfamily members exhibit a conserved heterotetrameric structure composed of two extracellular α-subunits for ligand binding and two transmembrane β-subunits containing the kinase domain, activated via ligand-induced trans-autophosphorylation to mediate overlapping roles in cellular growth and metabolism.^[11]

Structural and Functional Homologs

The insulin-like growth factor 1 receptor (IGF1R) has structural and functional homologs in various species that underscore its evolutionary conservation within the receptor tyrosine kinase family, particularly in regulating growth and metabolism. In Drosophila melanogaster, the insulin-like receptor (dIR, also known as InR) serves as a key homolog, sharing approximately 40-50% sequence identity in the kinase domain with human IGF1R and playing a central role in nutrient sensing, growth control, and lifespan regulation through binding to Drosophila insulin-like peptides (DILPs). Similarly, in Caenorhabditis elegans, the daf-2 gene encodes a receptor tyrosine kinase that is the ortholog of IGF1R, exhibiting sequence homology in the kinase domain and mediating insulin/IGF-1-like signaling to influence dauer formation, reproductive development, and longevity, with reduced daf-2 activity extending lifespan by up to twofold. A notable non-tyrosine kinase relative is the insulin-like growth factor 2 receptor (IGF2R), also known as the cation-independent mannose-6-phosphate receptor (CI-MPR), which evolved from an ancestral mannose-6-phosphate receptor and binds IGF-2 with high affinity but lacks an intracellular tyrosine kinase domain, thereby functioning primarily as a scavenger receptor to internalize and degrade IGF-2, preventing its interaction with signaling receptors like IGF1R. This contrasts with IGF1R's role in signal transduction, as IGF2R does not propagate growth-promoting signals and instead modulates IGF-2 bioavailability to maintain tissue homeostasis. Structural comparisons across these homologs reveal conserved features in ligand-induced conformational changes, with cryo-EM and crystal structures of apo (unliganded) and holo (ligand-bound) forms showing similar transitions from an autoinhibited, T-shaped dimer to an active, λ-shaped conformation upon ligand engagement, as observed in human IGF1R and dIR ectodomains. However, differences in ligand specificity are evident; for instance, dIR accommodates multiple DILPs with varying affinities due to its broader binding pocket in the L1 and cysteine-rich domains, unlike the more selective IGF-1 binding of human IGF1R. These shared structural motifs, including the leucine-rich repeats and fibronectin type III domains, highlight evolutionary divergence while preserving core activation mechanisms. Functional divergences among homologs illustrate specialized adaptations beyond growth regulation. The insulin receptor-related receptor (IRR), a close paralog of IGF1R in mammals, primarily functions as an extracellular alkali sensor, activated by mildly alkaline pH (above 7.4) rather than peptide ligands, with pH-induced proton dissociation in the L1 domain triggering autophosphorylation and downstream signaling in tissues like the kidney and inner ear that interface with external environments. This pH-sensing role in IRR contrasts sharply with IGF1R's focus on IGF-1-mediated anabolic processes, emphasizing how sequence homology can lead to distinct physiological contexts within the superfamily.

Activation and Signaling

Ligand Binding and Receptor Activation

The insulin-like growth factor 1 receptor (IGF1R) is primarily activated by its cognate ligands, insulin-like growth factor 1 (IGF-1) and insulin-like growth factor 2 (IGF-2). IGF-1 serves as the main agonist, exhibiting high binding affinity (Kd ≈ 0.1–1 nM) and produced predominantly by the liver as an endocrine hormone, with additional local synthesis in various tissues such as muscle and bone.^[16] In contrast, IGF-2 predominates during fetal development, with circulating levels 3–10 times higher than IGF-1 in the fetus, and displays lower affinity for IGF1R (Kd ≈ 10–100 nM) compared to IGF-1, though it binds with high affinity to the insulin receptor isoform A (IR-A).^[17] Structures reveal polymorphic ligand binding stoichiometries for IGF1R, including asymmetric 1:1 and symmetric 2:1 ligand:receptor ratios under saturating conditions, where ligands interact with the α-subunits to induce activation.^[7]^[18] Ligand engagement with the extracellular α-subunits triggers a series of conformational changes that relieve autoinhibition and activate the intracellular tyrosine kinase domains of the β-subunits. In the inactive state, the α-subunits are tethered in close proximity, constraining the β-subunits and preventing kinase activity; upon ligand binding, the α-subunits separate, allowing the transmembrane and intracellular regions to extend into an active configuration.^[7] This separation facilitates trans-autophosphorylation between the β-subunits, primarily at three conserved tyrosine residues in the activation loop (Tyr1131, Tyr1135, and Tyr1136 in the human sequence), located in the juxtamembrane and kinase domains.^[19] Phosphorylation at these sites stabilizes the active kinase conformation, enhancing catalytic activity by up to 100-fold.^[20] Cryo-electron microscopy (cryo-EM) structures have elucidated these dynamics, revealing a transition from a compact, autoinhibited "tethered" state to an extended, asymmetric "Γ-shaped" active form upon IGF-1 binding. For instance, the structure of the full-length mouse IGF1R in complex with human IGF-1 (PDB: 6PYH) at 4.3 Å resolution shows asymmetric 1:1 binding, with the ligand occupying a single binding site formed by the L1 domain and cysteine-rich region of one α-subunit and the C-terminal region of the other, promoting α-subunit dissociation and β-subunit dimerization for trans-phosphorylation.^[21] A 2022 structure of human IGF1R (PDB: 7YRR) further demonstrates symmetric 2:1 binding at site 2 epitopes.^[18] This asymmetric binding in 1:1 complexes reflects negative cooperativity, where initial ligand occupancy reduces affinity for a second ligand, though 2:1 binding indicates context-dependent activation.^[7] IGF1R can also form hybrid receptors with the structurally related insulin receptor (IR), influencing ligand specificity and activation profiles. These hybrids, composed of one IR αβ monomer and one IGF1R αβ monomer, include IR-A/IGF1R and IR-B/IGF1R variants, where IR-A is the exon-11-minus fetal isoform and IR-B is the exon-11-plus metabolic isoform.^[22] IR-A/IGF1R hybrids exhibit higher affinity for insulin (Kd ≈ 0.3 nM) compared to homotypic IGF1R (Kd > 100 nM), conferring greater insulin sensitivity, while both hybrid types respond preferentially to IGF-1 (approximately 20- to 50-fold higher potency than insulin) over IGF-2.^[23] In contrast, IR-B/IGF1R hybrids show reduced insulin binding, altering tissue-specific signaling in contexts like fetal growth and cancer.^[24]

Downstream Signaling Pathways

Upon ligand-induced dimerization and autophosphorylation of the insulin-like growth factor 1 receptor (IGF1R), primarily at tyrosine residues Tyr1131, Tyr1135, and Tyr1136 in the activation loop, the receptor recruits key adaptor proteins to initiate intracellular signaling. These include the insulin receptor substrates IRS-1 and IRS-2, which bind via their phosphotyrosine-binding domains to the phosphorylated juxtamembrane region (notably Tyr950), and the adaptor protein Shc, which also docks at Tyr950. Additionally, Grb2 binds to phosphorylated IRS or Shc, facilitating downstream activation.^[2]^[25] The primary downstream pathways activated by IGF1R include the PI3K/Akt/mTOR cascade, which promotes cell survival and metabolism, and the MAPK/ERK pathway, which drives proliferation. In the PI3K/Akt/mTOR pathway, phosphorylated IRS-1/2 recruits the p85 regulatory subunit of PI3K, leading to activation of its p110 catalytic subunit and generation of phosphatidylinositol (3,4,5)-trisphosphate (PIP3) at the plasma membrane. PIP3 then recruits and activates phosphoinositide-dependent kinase 1 (PDK1) and Akt (also known as PKB), with PDK1 phosphorylating Akt at Thr308 and mTORC2 at Ser473 for full activation; activated Akt subsequently stimulates mTORC1 to enhance protein synthesis and inhibit apoptosis.^[2]^[26]^[25] In parallel, the MAPK/ERK pathway is engaged through Grb2 binding to phosphorylated Shc or IRS, recruiting the guanine nucleotide exchange factor SOS to activate Ras, which in turn stimulates the Raf-MEK-ERK kinase cascade, culminating in ERK1/2 phosphorylation and nuclear translocation to regulate gene expression for cell growth and division. IGF1R also activates additional pathways, such as STAT3 via Janus kinase (JAK) phosphorylation, contributing to transcriptional regulation and anti-apoptotic effects, and phospholipase Cγ (PLCγ), which hydrolyzes PIP2 to produce inositol trisphosphate (IP3) and diacylglycerol (DAG), modulating calcium release and protein kinase C activity.^[2]^[27]^[28] IGF1R signaling exhibits crosstalk with the insulin receptor (IR), sharing adaptor proteins like IRS-1/2 and Shc, but IGF1R preferentially activates mitogenic pathways such as MAPK/ERK, whereas IR biases toward metabolic responses via enhanced PI3K/Akt signaling. This distinction arises from differential affinities for ligands and substrates, with hybrid IGF1R/IR receptors integrating signals in a context-dependent manner.^[29]^[2] To prevent excessive signaling, negative feedback mechanisms attenuate pathway activity, including serine phosphorylation of IRS-1/2 by downstream effectors such as S6K1 (activated by mTORC1) or components of the MAPK cascade, which promotes IRS ubiquitination and proteasomal degradation, thereby dampening PI3K recruitment and Akt activation.^[2]^[30]^[31]

Physiological Functions

Role in Embryonic and Postnatal Development

The insulin-like growth factor 1 receptor (IGF1R) is indispensable for embryonic development, as demonstrated by studies in knockout mouse models. Homozygous Igf1r-null mice display severe intrauterine growth retardation, with birth weights reduced to approximately 45% of wild-type littermates (a 55% reduction), and die shortly after birth due to respiratory failure stemming from muscle hypoplasia, underdeveloped diaphragms, and lung immaturity.^[32] This phenotype highlights the non-redundancy of IGF1R with the insulin receptor (IR), as IR-null mice exhibit embryonic lethality from hyperglycemia and organ atrophy but lack the profound muscle and skeletal defects seen in IGF1R deficiency.^[32] The absence of IGF1R signaling disrupts cell proliferation, survival, and differentiation across multiple tissues, underscoring its central role in coordinating embryonic morphogenesis. In skeletal muscle development, IGF1R promotes the proliferation and differentiation of myoblasts, which are critical precursors for muscle fiber formation. Activation of IGF1R by IGF-1 stimulates myoblast expansion during early myogenesis and subsequently drives their withdrawal from the cell cycle to fuse into multinucleated myotubes, enhancing muscle mass and function in the embryo.^[33] Similarly, in endochondral ossification, IGF1R signaling in chondrocytes of the growth plate facilitates hypertrophy, the terminal differentiation step where cells enlarge and secrete matrix to enable longitudinal bone elongation. IGF-1 exerts insulin-like effects to augment this hypertrophic response, independent of proliferation, thereby supporting the structural integrity of developing bones.^[34] Postnatally, IGF1R sustains linear growth through the growth hormone (GH)-IGF1 axis, in which pituitary-derived GH induces hepatic IGF-1 synthesis, and circulating IGF-1 binds IGF1R in peripheral tissues to promote chondrocyte activity in growth plates.^[35] This endocrine mechanism accounts for a substantial portion of postnatal body size increase, with IGF1R mediating local paracrine effects in proliferative zones. IGF1R expression is elevated in rapidly growing tissues such as the liver and bone during early postnatal life, correlating with heightened anabolic demands and facilitating the transition from embryonic to juvenile growth phases.^[36] In humans, IGF1R mutations are linked to intrauterine growth restriction (IUGR), characterized by low birth weight and head circumference, followed by severe postnatal growth failure. Heterozygous loss-of-function mutations, such as those impairing receptor kinase activity, reduce IGF-1 responsiveness and result in persistent short stature, often with birth weights below the third percentile and minimal catch-up growth.^[37] Compound heterozygous variants, including missense changes in the extracellular and tyrosine kinase domains, have been documented in cases of extreme pre- and postnatal growth impairment, emphasizing IGF1R's non-redundant contributions to human developmental growth.^[37]

Involvement in Metabolism and Lactation

The insulin-like growth factor 1 receptor (IGF1R) plays a key role in metabolic homeostasis by facilitating glucose uptake and lipogenesis in adipose and skeletal muscle tissues. Upon ligand binding, IGF1R activates the IRS-1/PI3K/AKT signaling pathway, which promotes translocation of glucose transporters (such as GLUT4) to the cell membrane, thereby enhancing insulin-stimulated glucose uptake in muscle cells.^[38] In adipose tissue, this pathway similarly supports glucose transport and drives de novo lipogenesis by upregulating enzymes like acetyl-CoA carboxylase and fatty acid synthase, contributing to fat storage and energy balance.^[39] While IGF1R signaling overlaps with that of the insulin receptor (IR) in these metabolic functions, it is distinguished by a stronger emphasis on proliferative effects rather than purely anabolic ones, as evidenced by tissue-specific differences in receptor activation and downstream gene expression.^[40] In the context of lactation, IGF1R is essential for mammary epithelial cell function, particularly in driving alveolar proliferation and the synthesis of milk proteins such as β-casein. During pregnancy and early lactation, IGF1R expression is upregulated in the mammary gland epithelium, where it synergizes with prolactin signaling to induce β-casein gene transcription via STAT5 activation and enhanced IGF-1 bioavailability.^[41] This interaction promotes alveolar differentiation and secretory capacity, ensuring efficient milk production; disruption of IGF1R signaling impairs these processes, leading to reduced β-casein expression and structural defects in alveolar architecture.^[42] Studies using conditional knockout models in mice highlight IGF1R's integration of metabolic and lactational roles. Mammary-specific dominant-negative IGF1R transgenics exhibit reduced alveolar proliferation during pregnancy, culminating in diminished milk protein synthesis and lower milk yield during lactation, which correlates with altered maternal glucose tolerance due to impaired nutrient partitioning toward the gland.^[42] These findings link IGF1R-mediated signaling to overall maternal metabolic adaptations, such as enhanced glucose uptake in mammary tissue to support lactose synthesis and energy demands of lactation.^[43] In humans, parallels emerge in gestational physiology, where increased IGF1R activation is observed in placentas from pregnancies with gestational diabetes mellitus and hyperglycemia, potentially promoting fetal growth through enhanced nutrient supply (particularly glucose and amino acids).^[44] This upregulation enhances IGF1R phosphorylation in trophoblast cells, promoting fetal nutrient supply but potentially exacerbating maternal hyperglycemia if unchecked.^[45]

Regulation of Body Size and Aging

The insulin-like growth factor 1 receptor (IGF1R) plays a central role in regulating body size through the growth hormone (GH)-IGF1 axis, where GH stimulates the liver and other tissues to produce IGF1, which then binds to IGF1R to promote somatic growth and linear height during development and adulthood.^[46] Expression levels of IGF1R in various tissues directly correlate with overall body size, as demonstrated in mouse models where altered receptor abundance influences proportional growth.^[47] Genetic polymorphisms in the IGF1R gene, particularly in promoter regions, contribute to height variation in human populations, with specific variants associated with modest differences in adult stature across diverse cohorts.^[48] In aging research, reduced IGF1R signaling has been shown to extend lifespan in model organisms by activating downstream pathways that enhance stress resistance and cellular maintenance. In Caenorhabditis elegans, mutations in daf-2, the homolog of IGF1R, approximately double the lifespan through activation of the DAF-16/FoxO transcription factor, which promotes longevity by upregulating genes involved in stress response and metabolism.^[49] This insulin/IGF-1 signaling pathway conservation highlights IGF1R's evolutionarily conserved role in modulating aging processes.^[50] In mammals, diminished IGF1R activity similarly promotes longevity, as seen in heterozygous Igf1r knockout mice (Igf1r^{+/-}), which exhibit extended lifespan compared to wild-type controls, accompanied by improved healthspan markers such as reduced oxidative damage.^[51] Dwarf mouse models with disrupted GH-IGF1 axis signaling, including low IGF1R activation, display approximately 40% lifespan extension, mimicking the effects of caloric restriction by boosting autophagy and resistance to metabolic stress without compromising fertility.^[52] Late-life reduction in IGF1R signaling further enhances these benefits, delaying age-related decline in physical function.^[53] Human studies link lower IGF1R signaling to exceptional longevity, with rare variants in the IGF1R gene identified in centenarians that impair receptor function and attenuate IGF1-mediated pathways, potentially contributing to prolonged lifespan.^[54] Offspring of long-lived individuals often show signs of reduced IGF1R sensitivity, such as elevated IGF1 levels relative to body size, supporting a balanced role for moderated signaling in maintaining vitality into advanced age.^[55] However, optimal IGF1R activity is necessary for preserving muscle mass and overall physical resilience, underscoring the importance of signaling equilibrium for healthy aging.^[56]

Pathological Roles

Association with Craniosynostosis and Growth Disorders

Overactive signaling through the insulin-like growth factor 1 receptor (IGF1R) contributes to craniosynostosis by accelerating the fusion of calvarial sutures through enhanced osteoblast proliferation and differentiation. In calvarial osteoblasts derived from patients with single-suture craniosynostosis (SSC), activation of the IGF1 pathway increases cellular contractility and motility, promoting premature suture closure.^[57] This pathway's dysregulation correlates with craniofacial defects in mouse models, where IGF1 overexpression leads to skeletal abnormalities including premature suture fusion via heightened osteoblast activity.^[57] Rare genetic variants in IGF1R have been identified in families with isolated craniosynostosis, particularly affecting single sutures such as the sagittal or coronal. A resequencing study of 130 SSC cases identified five rare missense variants in IGF1R, including three novel ones, that were significantly enriched compared to controls and segregated with the phenotype in affected families.^[58] These variants likely enhance IGF1R signaling, contributing to suture pathogenesis, and in some instances present with features resembling Saethre-Chotzen syndrome but without mutations in the TWIST1 gene.^[58] IGF1R mutations are also linked to various growth disorders, with inactivating variants causing short stature syndromes characterized by intrauterine and postnatal growth failure. Heterozygous loss-of-function mutations, such as nonsense or frameshift changes in the kinase domain, impair IGF1 signaling, resulting in resistance and often elevated serum IGF-1 levels.^[59] Recent studies as of 2025 have identified novel IGF1R variants associated with short stature, further delineating phenotypic variability.^[60] Conversely, gain-of-function alterations, including increased IGF1R copy number from 15q terminal duplications that encompass IGF1R, have been observed in overgrowth syndromes featuring tall stature and macrocephaly, though the specific contribution of IGF1R remains uncertain.^[61] In conditions like Beckwith-Wiedemann syndrome, upregulation of IGF2 can activate IGF1R signaling, contributing to overgrowth.

Effects of Gene Inactivation or Deletion

Inactivation or deletion of the IGF1R gene in model organisms reveals profound disruptions in growth and development, underscoring its essential role in prenatal and postnatal physiology. Homozygous null mutation of Igf1r in mice results in perinatal lethality, with embryos displaying a 45% reduction in body weight at birth compared to wild-type littermates, accompanied by severe muscle hypotrophy, delayed ossification, and abnormalities in skin development such as a thin epidermis and impaired dermal proliferation.^[32] These defects arise from impaired IGF-1 signaling, leading to respiratory failure shortly after birth. In contrast, heterozygous Igf1r null mice are viable but exhibit a consistent 20% reduction in adult body size and weight, with no overt lethality or major organ malformations, highlighting a gene dosage effect on somatic growth. Tissue-specific deletions of Igf1r further delineate its localized functions while revealing organ-specific vulnerabilities. Liver-specific knockout of Igf1r in mice does not substantially alter circulating IGF-1 levels, as hepatic IGF-1 production is primarily regulated by growth hormone via the growth hormone receptor rather than autocrine IGF1R signaling. Neuronal-specific deletion of Igf1r, particularly in the hippocampus and amygdala, disrupts synaptic plasticity and neurotransmitter receptor expression, resulting in impaired spatial learning, memory deficits, and increased anxiety-like behaviors in behavioral assays such as the elevated plus maze and Morris water maze. These effects demonstrate IGF1R's critical involvement in central nervous system maturation and function, with deficits emerging from reduced PI3K/Akt pathway activation in affected neurons. In humans, biallelic inactivating mutations in IGF1R, including homozygous nonsense and missense variants, cause severe intrauterine growth retardation (IUGR), microcephaly, and postnatal failure to thrive, often with additional features like developmental delay and dysmorphic facial traits. Such cases, first systematically reported in cohorts during the 2010s, typically result in birth weights below the 3rd percentile and head circumferences reduced by 2-3 standard deviations, reflecting profound impairment of IGF-1-mediated mitogenic signaling during embryogenesis. For instance, homozygous missense mutations in IGF1R disrupt receptor tyrosine kinase activity, leading to extreme short stature and metabolic dysregulation without complete lethality.^[62] Compensatory mechanisms partially mitigate IGF1R loss in certain contexts, particularly through upregulation of insulin receptor (IR)/IGF1R hybrid receptors, which form when IR and IGF1R monomers dimerize and retain partial affinity for IGF-1 ligands. In tissues like muscle and liver, these hybrids sustain some downstream signaling via shared PI3K/Akt and MAPK pathways, attenuating growth and metabolic defects in heterozygous or tissue-specific knockouts, though they cannot fully replicate homodimeric IGF1R functions.

Clinical Significance

Role in Cancer

The insulin-like growth factor 1 receptor (IGF1R) is frequently overexpressed in various human cancers, contributing to enhanced tumor cell proliferation and survival. In breast cancer, IGF1R upregulation occurs in approximately 50-90% of cases, particularly in estrogen receptor-positive subtypes, where it correlates with aggressive disease and reduced patient survival. Similarly, elevated IGF1R expression is observed in 60-80% of prostate cancers, promoting androgen-independent growth, while in lung and colorectal cancers, it is detected in over 70% of tumors, associating with advanced stages and poor prognosis.^[63]^[64]^[65] IGF1R exerts its oncogenic effects through autocrine and paracrine signaling loops involving IGF-1 and IGF-2 ligands, which activate the receptor to drive downstream pathways that inhibit apoptosis and enhance cell survival. For instance, IGF1R activation stimulates the PI3K/Akt pathway, conferring resistance to programmed cell death by upregulating anti-apoptotic proteins such as Bcl-2. Additionally, IGF1R promotes tumor metastasis by inducing epithelial-mesenchymal transition (EMT), a process that increases cell motility and invasiveness through transcriptional changes in E-cadherin and vimentin expression. These mechanisms underscore IGF1R's role in sustaining tumor progression beyond initial proliferation signals.^[66]^[67]^[68] In specific malignancies, IGF1R plays distinct roles that amplify cancer hallmarks. In hepatocellular carcinoma, IGF1R signaling drives angiogenesis by upregulating vascular endothelial growth factor (VEGF) expression in tumor cells, facilitating nutrient supply and metastatic spread. In multiple myeloma, IGF1R supports the survival of malignant plasma cells within the bone marrow niche, where it interacts with stromal cells to provide protective signals against apoptosis and chemotherapy-induced death.^[69]^[70]^[71] As a prognostic biomarker, high IGF1R expression predicts increased metastasis risk across several cancers. In breast cancer, particularly ERBB2 (HER2)-enriched subtypes, co-expression of IGF1R and ERBB2 amplifies signaling crosstalk, correlating with worse overall survival and resistance to targeted therapies.^[72]^[73] The insulin-like growth factor 1 receptor (IGF1R) plays a significant role in the pathogenesis of type 2 diabetes and insulin resistance. Activation of IGF1R signaling contributes to compensatory β-cell hyperplasia in response to chronic hyperglycemia, as evidenced by studies showing that IGF1R-mediated pathways, particularly through IRS-2, promote β-cell proliferation to offset insulin demand in insulin-resistant states.^[74] However, formation of hybrid receptors between IGF1R and the insulin receptor (IR) disrupts normal insulin signaling, as these hybrids exhibit high affinity for IGF-1 but low affinity for insulin, leading to reduced glucose uptake and exacerbated hyperglycemia.^[23] Increased prevalence of such hybrids in adipose and skeletal muscle tissues of individuals with type 2 diabetes correlates with diminished insulin sensitivity and contributes to systemic insulin resistance.^[75] In age-related neurodegenerative diseases, dysregulated IGF1R signaling is implicated in pathological processes. Elevated IGF1R activity has been linked to Alzheimer's disease progression through promotion of tau hyperphosphorylation, a hallmark of neurofibrillary tangle formation, as IGF-1 stimulation activates downstream kinases like GSK-3β that phosphorylate tau.^[76] In Parkinson's disease, reduced IGF1R/IGF-1 signaling is associated with disease progression, as partial IGF-1 deficiency exacerbates oxidative damage, inflammation, and neuronal apoptosis in toxin-induced models like MPTP, highlighting the neuroprotective role of adequate IGF1R activity in preventing microglial activation and dopaminergic neuron loss.^[77] IGF1R influences cardiovascular health, particularly in atherosclerosis, by regulating vascular smooth muscle cell (VSMC) behavior. IGF1R signaling promotes VSMC proliferation and migration, which stabilizes atherosclerotic plaques by increasing collagen content and fibrous cap thickness, thereby reducing rupture risk; deficiency in VSMC-specific IGF1R leads to plaque instability, larger necrotic cores, and accelerated lesion progression in hyperlipidemic models.^[78] Additionally, low IGF1R activity, reflected by reduced circulating IGF-1 levels, correlates with increased frailty in the elderly, independently associating with higher odds of frailty (adjusted OR 1.54 for lowest vs. highest IGF-1 quartile) due to impaired muscle maintenance and physical resilience.^[79] Recent genome-wide association studies (GWAS) post-2020 have identified IGF1R variants influencing metabolic and longevity outcomes. Rare loss-of-function variants in IGF1R, such as those reducing receptor signaling, are enriched in centenarians and linked to extended lifespan by mimicking caloric restriction effects on insulin/IGF-1 pathways.^[80] Similarly, damaging missense variants in IGF1R confer risk for metabolic syndrome and type 2 diabetes in diverse populations, highlighting its role in glucose homeostasis and age-related metabolic decline.^[81] Emerging evidence as of 2025 also associates IGF1R dysregulation with increased risk of frontotemporal dementia and metabolic complications in long COVID survivors, expanding its clinical implications in age-related and post-viral conditions.^[82]

Regulation and Interactions

Post-Translational Regulation

The insulin-like growth factor 1 receptor (IGF1R) is subject to multiple post-translational modifications that fine-tune its activation, stability, trafficking, and subcellular localization following protein synthesis. Among these, phosphorylation plays a central role in modulating receptor function beyond initial ligand-induced autophosphorylation on key tyrosine residues in the activation loop. Inhibitory phosphorylation occurs on serine residues within the C-terminal tail, such as Ser1280–1283, mediated by kinases including protein kinase C (PKC), which attenuates kinase activity and downstream signaling.^[2] Dephosphorylation by protein tyrosine phosphatase 1B (PTP1B) reverses activating tyrosine phosphorylations on IGF1R, while phosphatase and tensin homolog (PTEN) dephosphorylates PIP3 to attenuate downstream signaling, thereby dampening signaling intensity and duration in response to stimuli like oxidative stress or nutrient deprivation.^[83]^[84] Ubiquitination serves as a critical mechanism for controlling IGF1R turnover, particularly during prolonged ligand stimulation. The E3 ubiquitin ligase c-Cbl promotes K48-linked ubiquitination of the receptor, facilitating clathrin-mediated endocytosis, trafficking to lysosomes, and subsequent proteolytic degradation, which prevents sustained signaling and maintains cellular homeostasis.^[85] This process is tyrosine kinase-dependent, requiring initial receptor autophosphorylation, and involves adaptors like β-arrestin to recruit c-Cbl to the endocytic machinery.^[86] Glycosylation is essential for IGF1R maturation and function, with N-linked glycans on the α-subunit playing a pivotal role in proper folding, proteolytic processing of the proreceptor, and high-affinity ligand binding. Defects in N-glycosylation, as seen in congenital disorders, lead to endoplasmic reticulum retention, reduced surface expression, and impaired signaling.^[87] Additionally, O-GlcNAcylation, a dynamic nutrient-sensitive modification, modulates IGF1R kinase activity by promoting autophosphorylation, likely through inhibition of PTP1B, thereby enhancing PI3K/Akt pathway activation under hyperglycemic conditions.^[88] Other modifications include SUMOylation and palmitoylation, which influence IGF1R localization. SUMO-1 conjugation on conserved lysine residues (Lys1025, Lys1100, Lys1120) in the β-subunit, induced by IGF-1, enables nuclear translocation of the receptor, where it acts as a transcriptional co-activator independent of its canonical kinase signaling.^[89] Palmitoylation, indirectly regulating IGF1R via the scaffold protein flotillin-1, controls receptor trafficking from the endoplasmic reticulum to the plasma membrane; depalmitoylation-repalmitoylation cycles sustain kinase activation upon ligand binding.^[90]

Protein-Protein Interactions

The insulin-like growth factor 1 receptor (IGF1R) participates in a diverse array of non-covalent protein-protein interactions that modulate its activation, localization, and downstream signaling without involving post-translational modifications. These interactions typically occur at the phosphorylated tyrosine residues within the receptor's intracellular kinase domain, serving as docking sites for adaptor proteins and coregulators that fine-tune IGF1R function in various cellular contexts.^[2] Key adaptor proteins include insulin receptor substrates 1 and 2 (IRS-1 and IRS-2), which bind directly to autophosphorylated IGF1R through their phosphotyrosine-binding (PTB) domains. This interaction recruits the p85 regulatory subunit of phosphatidylinositol 3-kinase (PI3K) to IRS proteins, thereby initiating the PI3K-Akt pathway essential for metabolic and proliferative responses.^[91] In parallel, the adaptor protein Shc docks to tyrosine-phosphorylated IGF1R and associates with growth factor receptor-bound protein 2 (Grb2), which recruits son of sevenless (Sos) to activate the Ras-mitogen-activated protein kinase (MAPK) cascade, promoting cell growth and differentiation.^[2] Among coregulators, caveolin-1 binds IGF1R within plasma membrane lipid rafts, sequestering the receptor in these cholesterol-rich microdomains to inhibit its activation and downstream signaling, such as in adipocyte differentiation processes.^[92] Similarly, β-arrestin interacts with IGF1R after G-protein-coupled receptor kinase (GRK)-mediated phosphorylation of the receptor's C-terminal tail, facilitating rapid desensitization, endocytosis, and signal attenuation to prevent prolonged activation.^[93] IGF1R also forms functional hybrids through dimerization with the insulin receptor (IR), creating heterotetrameric complexes composed of one IGF1R αβ monomer and one IR αβ monomer; these hybrids exhibit biased ligand affinity, with insulin preferentially activating hybrid signaling toward metabolic outcomes rather than mitogenic ones.^[94] In cancer contexts, IGF1R heterodimerizes with the epidermal growth factor receptor (EGFR), enabling crosstalk that stabilizes IGF1R expression, enhances PI3K-Akt and MAPK pathway activation, and contributes to resistance against EGFR-targeted therapies.^[95] Interaction databases highlight the breadth of IGF1R's binding partners, underscoring its role as a signaling hub. The BioGRID database catalogs 526 unique interactors for human IGF1R, derived from experimental evidence including affinity capture and co-immunoprecipitation assays.^[96] Prominent among these are PIK3R1 (the p85 subunit of PI3K) and MAPK1 (Erk2), which rank highly due to frequent co-occurrence in signaling complexes, as evidenced by high-confidence networks in resources like STRING.^[3]

Therapeutic Targeting

Inhibitors and Modulators

The insulin-like growth factor 1 receptor (IGF1R) has been targeted by various pharmacological agents, primarily to disrupt its role in cell proliferation and survival signaling. Monoclonal antibodies represent a key class of inhibitors, with figitumumab (CP-751,871) being a fully human IgG2 antibody that selectively binds to the α-subunit of IGF1R, thereby blocking ligand access by IGF-1 and IGF-2 and promoting receptor internalization and degradation.^[97] This mechanism inhibits IGF1R autophosphorylation and downstream signaling, leading to antiproliferative effects in preclinical models.^[98] However, development of figitumumab was discontinued following phase III trials due to lack of efficacy in improving outcomes, such as in non-small cell lung cancer.^[99] Tyrosine kinase inhibitors (TKIs) constitute another major category, exemplified by linsitinib (OSI-906), a small-molecule dual inhibitor of IGF1R and the insulin receptor (IR). Linsitinib competitively binds to the ATP-binding site of the IGF1R kinase domain, preventing autophosphorylation and activation of downstream pathways like PI3K/AKT.^[100] This agent has been evaluated in clinical trials, including for adrenocortical carcinoma, where it demonstrated preliminary antitumor activity despite challenges in broader application and subsequent termination of development.^[101]^[102] Other modulators include antisense oligonucleotides (ASOs) that target IGF1R mRNA to reduce receptor expression. For instance, 2′-MOE-modified ASOs bind to IGF1R mRNA sequences, inducing RNase H-mediated degradation and thereby decreasing IGF1R protein levels, which inhibits tumor cell proliferation in vitro and in vivo models.^[103] Similarly, natural compounds like genistein, a soy isoflavone, act as partial antagonists by inactivating IGF1R and suppressing phosphorylation of downstream effectors such as AKT, contributing to antiproliferative and pro-apoptotic effects in cancer cells.^[104] Development of IGF1R inhibitors faces significant challenges, including toxicity from cross-inhibition of IR, which disrupts glucose homeostasis and causes hyperglycemia.^[105] Additionally, resistance often arises through pathway crosstalk, where IGF1R inhibition leads to compensatory activation of alternative signaling networks, such as EGFR or MAPK pathways, thereby limiting therapeutic efficacy.^[106]

Clinical Applications and Challenges

The clinical translation of IGF1R-targeted therapies has shown mixed results, with notable successes in specific pediatric sarcomas but broader challenges in solid tumors. In a phase I/II trial of figitumumab monotherapy in patients with refractory Ewing sarcoma, the objective response rate was 2%, with stable disease in 29% of patients.^[107] However, trials in non-small cell lung cancer (NSCLC) have largely failed to demonstrate significant efficacy, attributed to intratumoral heterogeneity in IGF1R expression and signaling, which complicates patient selection and leads to inconsistent responses across cohorts.^[108] These outcomes highlight the potential of IGF1R inhibition in IGF1R-overexpressing tumors like Ewing sarcoma while underscoring the need for refined trial designs in heterogeneous cancers such as NSCLC.^[109] Combination strategies have emerged to enhance IGF1R-targeted efficacy by addressing resistance mechanisms, particularly in aggressive malignancies. For instance, dual inhibition of IGF1R and vascular endothelial growth factor (VEGF) pathways has been explored in glioblastoma, where preclinical models demonstrate that anti-VEGF agents like bevacizumab upregulate IGF1 signaling, and combined blockade suppresses tumor growth more effectively than monotherapy.^[110] Similarly, pairing IGF1R inhibitors with PD-1 checkpoint inhibitors shows promise in overcoming immunosuppressive microenvironments; an ongoing phase I trial (NCT06866548) as of November 2025 evaluates an anti-IGF1R monoclonal antibody with anti-PD-1 therapy in metastatic castration-resistant prostate cancer, aiming to boost T-cell infiltration and response rates.^[111] Completed trials like AEWS1221 (NCT02306161), which added ganitumab to chemotherapy in newly diagnosed metastatic Ewing sarcoma, did not improve event-free survival but informed ongoing research into IGF pathway targeting in pediatric sarcomas as of 2025.^[112] Biomarker-driven approaches are critical for optimizing IGF1R therapies, focusing on expression, ligand levels, and pathway activation. Immunohistochemistry (IHC) assessment of IGF1R expression in tumor biopsies serves as a primary predictive biomarker, with high membranous staining correlating to potential responsiveness in sarcomas and other IGF1R-dependent cancers.^[113] Circulating IGF-1 levels provide a non-invasive surrogate, as elevated serum IGF-1 is associated with increased IGF1R signaling and poorer prognosis in multiple tumor types, guiding patient enrollment.^[114] For pharmacodynamic monitoring, phosphorylation of IGF1R (p-IGF1R) in peripheral blood mononuclear cells or tumor tissue post-treatment confirms target engagement and inhibition, enabling dose adjustments in real-time during trials.^[115] Despite these advances, clinical challenges persist, limiting widespread adoption of IGF1R-targeted therapies. Dose-limiting toxicities, such as thrombocytopenia (observed in up to 28% of patients across anti-IGF1R monoclonal antibody trials), hyperglycemia, and fatigue, necessitate careful management and often restrict dosing intensity.^[116] Compensatory upregulation of the insulin receptor (IR) or activation of alternative pathways, like PI3K/AKT, frequently emerges as a resistance mechanism, reducing long-term efficacy even in initially responsive tumors.^[114] Patient stratification remains a key barrier, as heterogeneous biomarker profiles and lack of robust predictive tools lead to inclusion of non-responders, inflating failure rates in unselected populations.^[117] Ongoing research as of 2025 emphasizes integrating multi-omics profiling to address these issues and improve therapeutic precision, with 2025 reviews noting promise in next-generation IGF1R inhibitors combined with immunotherapy.^[118]

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In 3T3-L1 cells, IGF-1 receptor is located in lipid rafts/caveolae of the plasma membrane and can directly interact with caveolin-1, the major protein component ...
[92]
Functional antagonism of β-arrestin isoforms balance IGF-1R ...
Jun 5, 2017 · β-arrestin recruitment and binding to the ligand-stimulated receptor is essential for desensitization, sequestration, recycling and ...
[93]
The insulin and IGF1 receptor kinase domains are functional dimers ...
Mar 11, 2015 · Here we provide crystallographic, biophysical and biochemical evidence demonstrating that the phosphorylated kinase domains of IR and IGF1R form ...
[94]
The EGF receptor interacts with the type 1 IGF ... - ScienceDirect.com
These results indicate novel evidence of crosstalk between two key cancer treatment targets, capable of modifying the stability of IGF1R protein.
[95]
IGF1R Result Summary - BioGRID
Chemical Interactions 16; Network; PTM Sites 45. Showing 1 to 300 of 526 unique interactors.Missing: STRING | Show results with:STRING
[96]
The insulin-like growth factor-I receptor inhibitor figitumumab (CP ...
Jul 13, 2010 · Figitumumab blocks the binding of IGF-1 to IGF-IR, inhibits the downstream signalling activated by both IGF-1 and IGF-2, and induces prolonged ...Materials And Methods · Pharmacokinetics · Pharmacodynamics
[97]
Safety, pharmacokinetics, and preliminary activity of the anti-IGF-1R ...
Figitumumab (previously CP-751,871) is a highly specific, fully human IgG2 monoclonal antibody that inhibits IGF-1R autophosphorylation induced by IGF-I and IGF ...
[98]
Update of IGF-1 receptor inhibitor (ganitumab, dalotuzumab ...
Apr 25, 2017 · ... Figitumumab (CP-751,871) (HR = 1.14, 95% CI = 1.00-1.29), indicating that figitumumab (CP-751,871) may be harmful on cancer treatment. Two ...
[99]
Phase I Dose-Escalation Study of Linsitinib (OSI-906) and Erlotinib ...
Linsitinib (OSI-906) is a potent, orally bioavailable dual IGF1R and INSR tyrosine kinase inhibitor (TKI) with antiproliferative effects in a variety of tumor ...
[100]
Linsitinib (OSI-906) versus placebo for patients with ... - PubMed
Linsitinib (OSI-906) versus placebo for patients with locally advanced or metastatic adrenocortical carcinoma: a double-blind, randomised, phase 3 study.Missing: mechanism | Show results with:mechanism
[101]
Antisense oligonucleotide targeting insulin-like growth factor-1 ...
Apr 15, 2010 · In this study, we assess the potency and anti-cancer activity of a 2′-MOE-modified antisense oligonucleotide (ASO) targeting human IGF-IR, ...
[102]
Genistein induces apoptosis by the inactivation of the IGF-1R/p-Akt ...
Furthermore, genistein induced the inactivation of IGF-1R and p-Akt and downregulated the Bcl-2/Bax protein ratio. These results suggest that genistein ...
[103]
Targeting the Insulin-Like Growth Factor (IGF) System Is Not as ...
Most therapeutic strategies have been designed to specifically inhibit IGF-1R but have for the most part ignored the insulin receptor (IR).
[104]
Drugging IGF-1R in cancer: New insights and emerging opportunities
Here we review the occurrence of IGF-1R aberrations and activation mechanisms in cancers, which justify the development of anti-IGF-1R therapies.
[105]
R1507, a Monoclonal Antibody to the Insulin-Like Growth Factor 1 ...
Oct 24, 2011 · The overall complete response/partial response rate was 10% (95% CI, 4.9% to 16.5%). The median duration of response was 29 weeks (range, 12 to ...
[106]
Costs and Causes of Oncology Drug Attrition and Insulin-Like ...
Jul 28, 2023 · It is possible that discovery and improved use of biomarkers for IGF-1R inhibitors could reduce these examples of clinical trial failure, ...Missing: NSCLC | Show results with:NSCLC
[107]
IGF-1R inhibitors in cancer: A review of available evidence and ...
Clinical trials with IGF-1R inhibitors have mostly focused on breast cancer, gastrointestinal cancers, and NSCLC, with more than 100 clinical trials involving ...
[108]
Targeting the Insulin Growth Factor and the Vascular Endothelial ...
Here, we report that the insulin growth factor-1 (IGF-1) is upregulated during treatment with bevacizumab of ovarian xenografts and show that dual anti-VEGF and ...In Vivo Anti-Vegf And Igf... · Results · Anti-Igf And -Vegf Therapy...
[109]
Safety and Efficacy Evaluation of Anti IGF-1R Monoclonal Antibody ...
This trial is designed to evaluate the safety and efficacy of anti-IGF-1R mAb in combination with anti-PD-1 mAb in patients with mCRPC. Detailed Description.
[110]
[PDF] NCI Protocol #: 10003 Version Date: 04/06/2020 - Clinical Trials
Jun 4, 2020 · antitumor effect by inhibiting IGF1R activation through blockade of ligand binding (IGF-1 and ... (51) = 0.30 nM), cynomolgus monkey (Kd = 0.15 nM) ...
[111]
A dose finding, safety and pharmacokinetic study of AVE1642, an ...
Using immunohistochemistry assays (IHC), IGF-1R expression and occupancy by AVE1642 were evaluated. Two different antibodies were needed to perform this test.
[112]
IGF-1R targeting in cancer – does sub-cellular localization matter?
Oct 20, 2023 · IGF-1R does not contain a nuclear localization signal (NLS), hence active mechanisms of nuclear import must contribute to nuclear localization.Missing: composition heterotetrameric
[113]
BI 885578, a Novel IGF1R/INSR Tyrosine Kinase Inhibitor with ...
Abstract. Inhibition of the IGF1R, INSRA, and INSRB receptor tyrosine kinases represents an attractive approach of pharmacologic intervention in cancer,
[114]
The adverse events profile of anti-IGF-1R monoclonal antibodies in ...
Our purpose was to conduct a systematic review of the adverse events (AEs) caused by anti-IGF-1R monoclonal antibodies in cancer therapy.
[115]
sticking points in understanding IGF1R function in cancer
Discourse in the literature has acknowledged that a lack of patient stratification may have impacted success of IGF1R inhibitor trials. This argument alludes to ...<|control11|><|separator|>