| 2019 |
IGF2BP2 acts as an m6A 'reader' that recognizes and binds m6A-modified SOX2 mRNA specifically at coding sequence (CDS) regions, preventing SOX2 mRNA degradation and thereby maintaining SOX2 expression in colorectal cancer cells downstream of METTL3. |
MeRIP-seq, RNA pull-down, RNA immunoprecipitation, RNA stability assay |
Molecular cancer |
High |
31230592
|
| 2019 |
LncRNA LINRIS binds IGF2BP2 and blocks K139 ubiquitination of IGF2BP2, preventing its degradation through the autophagy-lysosome pathway (ALP), thereby stabilizing IGF2BP2 protein and sustaining MYC-mediated glycolysis in colorectal cancer cells. |
RNA pull-down, RIP assay, ubiquitination assay, autophagy-lysosome pathway inhibition experiments |
Molecular cancer |
High |
31791342
|
| 2019 |
IGF2BP2 binds m6A-modified lncRNA DANCR (with the critical adenosine at position 664 identified by mutagenesis) and stabilizes DANCR RNA, promoting cancer stemness-like properties in pancreatic cancer. |
In vivo RNA precipitation, reciprocal RNA immunoprecipitation, mutagenesis assay of m6A site |
Cell death and differentiation |
High |
31804607
|
| 2022 |
IGF2BP2 promotes AML development and leukemia stem/initiation cell self-renewal by regulating expression of MYC, GPT2, and SLC1A5 in the glutamine metabolism pathway in an m6A-dependent manner; inhibition by small-molecule CWI1-2 shows anti-leukemia effects. |
m6A-dependent target gene regulation assays, small-molecule inhibitor (CWI1-2) in vitro and in vivo, loss-of-function with defined phenotypic readouts |
Cancer cell |
High |
36306790
|
| 2022 |
IGF2BP2 binds m6A-modified TAB3 mRNA at stop codon regions, enhancing TAB3 mRNA stability; this is downstream of METTL3-mediated m6A modification and promotes renal inflammation. |
MeRIP-seq, RIP assay, RNA stability assay, conditional METTL3 knockout mouse model |
Science translational medicine |
High |
35417191
|
| 2022 |
IGF2BP2 recognizes m6A-modified EphA2 and VEGFA mRNAs (written by METTL3) and prevents their degradation, promoting vasculogenic mimicry in colorectal cancer via PI3K/AKT/mTOR and ERK1/2 signaling. |
CRISPR/Cas9 knockdown, RNA-seq, RIP assay, m6A reader binding confirmation |
Cell death & disease |
Medium |
35595748
|
| 2020 |
IGF2BP2 directly recognizes and binds the m6A site on FEN1 mRNA, enhancing FEN1 mRNA stability and promoting hepatocellular carcinoma proliferation in vitro and in vivo. |
RIP assay, RNA stability assay, overexpression and knockdown in vitro and in vivo |
Frontiers in oncology |
Medium |
33224879
|
| 2022 |
IGF2BP2 stabilizes m6A-modified Slug mRNA by binding the m6A site in the CDS region of Slug, promoting EMT and lymphatic metastasis in head and neck squamous cell carcinoma. |
RIP, MeRIP, luciferase reporter assay, mRNA stability assay, in vivo lymphatic metastasis model |
Journal of experimental & clinical cancer research |
High |
34980207
|
| 2010 |
IMP-2 (IGF2BP2) directly binds the mRNAs of PINCH-2 and MURF-3 (confirmed by gel shift experiments), regulating their protein expression; upregulation of PINCH-2 in IMP-2-depleted myoblasts is the key event responsible for decreased cell motility; IMP-2 is also required for microtubule stabilization. |
Gel shift (EMSA), gain- and loss-of-function assays, transcript binding analysis |
Molecular and cellular biology |
High |
20956565
|
| 2022 |
CircEZH2 interacts with IGF2BP2 and blocks its ubiquitination-dependent degradation, stabilizing IGF2BP2; additionally, the circEZH2/IGF2BP2 complex enhances CREB1 mRNA stability in colorectal cancer. |
RNA pulldown, mass spectrometry, RIP, MeRIP-seq, western blot, luciferase reporter assays |
Molecular cancer |
Medium |
35773744
|
| 2021 |
SUMOylation of IGF2BP2 at lysine residues K497, K505, and K509 (primarily via SUMO1) increases IGF2BP2 protein stability by blocking its ubiquitin-proteasome degradation; this modification can be reversed by SENP1. SUMOylated IGF2BP2 enhances OIP5-AS1 lncRNA stability and promotes glioma vasculogenic mimicry. |
Ni2+-NTA agarose bead pull-down, Co-IP, western blot, in vitro SUMOylation assay, immunoprecipitation, immunofluorescence, RIP, luciferase reporter assays |
International journal of biological sciences |
High |
34345216
|
| 2022 |
IGF2BP2 binds to the 3'UTR of the ATP6V1A transcript and, when acetylated (due to low SIRT1 expression), recruits the XRN2 nuclease to mediate ATP6V1A transcript degradation. When SIRT1 deacetylates IGF2BP2, binding occurs but degradation does not. Thus, SIRT1-regulated acetylation of IGF2BP2 switches its function from mRNA protection to mRNA degradation. |
RNA binding assays, SIRT1 deacetylation assay, XRN2 recruitment assay, mRNA stability measurement, SIRT1 knockdown |
Proceedings of the National Academy of Sciences of the United States of America |
High |
36322753
|
| 2021 |
IMP2/IGF2BP2 directly binds Pdx1 mRNA and stimulates its translation in an m6A-dependent manner; additionally, IMP2 orchestrates IGF2-AKT-GSK3β-PDX1 signaling to stabilize PDX1 protein, promoting pancreatic β-cell proliferation and insulin secretion. |
Pancreatic β-cell-specific Imp2 knockout mice, RIP assay, m6A-dependent translation assay, signaling pathway analysis |
Molecular metabolism |
High |
33705986
|
| 2018 |
Airn lncRNA binds IGF2BP2 (identified by RNA pull-down/mass spectrometry) and controls translation of several IGF2BP2-target genes in cardiomyocytes; silencing Airn reduces binding of IGF2BP2 to other mRNAs and reduces IGF2BP2 protein translation. |
RNA pull-down followed by mass spectrometry, further RIP assays, siRNA silencing |
Circulation research |
Medium |
29483092
|
| 2016 |
IGF2BP2 regulates RAF1 expression in colorectal cancer cells by protecting RAF1 mRNA from degradation by miR-195, functioning as a post-transcriptional regulatory factor that interferes with miRNA-mediated mRNA degradation. |
Overexpression and shRNA-mediated silencing, molecular function analyses |
FEBS letters |
Medium |
27153315
|
| 2016 |
IGF2BP2 is a downstream target of HMGB2 in myoblasts; IGF2BP2 binds mRNAs of Myf5 and cyclin A2, enhancing Myf5 translation and cyclin A2 mRNA stabilization, respectively. Overexpression of IGF2BP2 partially rescues Myf5 and cyclin A2 protein levels upon HMGB2 depletion. |
Knockdown/overexpression rescue experiments, western blot, in vivo satellite cell depletion model |
Journal of cell science |
Medium |
27672022
|
| 2019 |
Maternal deletion of Igf2bp2 (IMP2) in mouse embryos causes developmental arrest at the 2-cell stage; IMP2 regulates expression of Ccar1 and Rps14 required for zygotic genome activation, and IGF2 (a known IMP2 target) addition rescues developmental competence. |
Maternal-specific conditional knockout mice, transcriptomics, proteomics, embryo culture rescue assays |
Advanced science |
High |
31406667
|
| 2022 |
IGF2BP2 promotes cell cycle progression in TNBC by recognizing m6A-modified CDK6 mRNA and enhancing its translation initiation (not mRNA stability) by recruiting EIF4A1; this is dependent on m6A modification. |
m6A-dependent translation assay, RIP, mRNA stability assay (showing no effect), EIF4A1 co-immunoprecipitation, CDK6 reporter assays |
Advanced science |
High |
37983610
|
| 2022 |
FBW7 (ubiquitin ligase) works together with GSK3β kinase to recognize and degrade IGF2BP2 through ubiquitination; conversely, IGF2BP2 enhances SLC7A5 mRNA stability and translation through m6A modification, with SLC7A5-mediated methionine transport feeding back to increase H3K4me3 at the IGF2BP2 promoter, forming a positive feedback loop promoting lung cancer radioresistance. |
Ubiquitination assays, Co-IP, ChIP-qPCR, RIP, MeRIP-qPCR, RNA pull-down |
Journal of experimental & clinical cancer research |
High |
38281999
|
| 2023 |
IGF2BP2 promotes liver cancer progression by recognizing and binding m6A-modified FLT4 mRNA (secreted via exosomes to endothelial cells), improving FLT4 RNA stability and activating the PI3K-Akt signaling pathway to promote angiogenesis. |
Single-cell RNA sequencing, exosome isolation, m6A modification assay, PI3K-Akt pathway analysis |
Molecular cancer |
Medium |
37353784
|
| 2022 |
IGF2BP2 recognizes m6A modification sites in IGF1R mRNA, increases IGF1R expression, and activates the RhoA-ROCK pathway to promote gastric cancer progression; this was confirmed by RIP and RNA pull-down assays. |
RIP assay, RNA pull-down, qRT-PCR, western blot, in vitro and in vivo functional assays |
Cellular signalling |
Medium |
35306138
|
| 2023 |
IGF2BP2 promotes glycolysis and hepatic stellate cell activation by stabilizing ALDOA (Aldolase A) mRNA via m6A-binding, generating lactate that drives histone lactylation to sustain the activated phenotype of hepatic stellate cells. |
m6A binding assay, mRNA stability assay, glycolysis measurement, histone lactylation analysis, loss-of-function experiments |
Cell death & disease |
Medium |
38443347
|
| 2022 |
IGF2BP2 binds to circRUNX1 and prevents its degradation; IGF2BP2-stabilized circRUNX1 sponges miR-449b-5p to upregulate FOXP3, facilitating esophageal squamous cell carcinoma growth and metastasis. |
RIP assay, RNA immunoprecipitation, RNA sequencing, dual-luciferase reporter assays, rescue experiments |
Journal of experimental & clinical cancer research |
Medium |
36522683
|
| 2022 |
CircRHBDD1 binds to IGF2BP2 and disrupts the interaction between E3 ligase TRIM25 and IGF2BP2, inhibiting IGF2BP2 ubiquitination and degradation; stabilized IGF2BP2 then enhances PD-L1 mRNA stability through m6A modification to promote immune escape in gastric cancer. |
RNA immunoprecipitation, Co-IP, meRIP analysis, ubiquitination assay, flow cytometry |
Journal of translational medicine |
Medium |
39080693
|
| 2024 |
METTL14-mediated m6A modification stabilizes GluN2A subunit (NMDAR) expression via IGF2BP2 in DRG neurons; METTL14-mediated m6A facilitates synaptic plasticity and pain hypersensitivity through this IGF2BP2-dependent mechanism. |
Dot blotting, immunofluorescence, gain/loss-of-function, behavioral assays, RIP (implied from m6A-IGF2BP2-dependent mechanism) |
The Journal of clinical investigation |
Medium |
38319733
|
| 2024 |
METTL14-mediated m6A modification of NLRP3 mRNA is recognized by IGF2BP2, which stabilizes NLRP3 mRNA; IGF2BP2 knockdown diminishes LPS-induced acute lung injury in mice by downregulating NLRP3 expression. |
MeRIP, RIP assay, in vitro macrophage experiments, mouse ALI model with IGF2BP2 knockdown |
Cell death & disease |
High |
38218935
|
| 2022 |
Igf2bp2 deletion in young mice reduces oxidative metabolism and impairs colony formation and HSC repopulation capacity, mimicking aging-related changes; Igf2bp2-deficient aged mice show amelioration of aging-associated HSC expansion and myeloid skewing, indicating Igf2bp2 regulates mitochondrial metabolism and stemness of young HSCs. |
Igf2bp2 knockout mouse model, RNA sequencing, colony formation assays, bone marrow transplantation/repopulation assays |
Blood |
High |
35231105
|
| 2023 |
LCAT1 lncRNA physically interacts with and stabilizes IGF2BP2 by preventing its degradation via autolysosomes; the LCAT1/IGF2BP2 complex then increases CDC6 mRNA levels by stabilizing CDC6 mRNA in an m6A-dependent manner, promoting lung cancer progression. |
RNA pulldown, Co-IP, RIP, m6A-dependent mRNA stability assay |
Cell death & disease |
Medium |
36257938
|
| 2023 |
IGF2BP2 overexpression in cardiomyocytes leads to dilated cardiomyopathy (DCM) with downregulation of sarcomeric and mitochondrial proteins and fragmented mitochondria; downregulating the IGF2BP2 transgene after 2 weeks rescues DCM, demonstrating reversible pathological role. |
Conditional inducible transgenic mouse model, cardiac phenotyping, proteomics |
Communications biology |
High |
38052926
|
| 2023 |
IMP2/IGF2BP2 binds Wnt receptor Fzd8 mRNA and promotes its degradation by recruiting the CCR4-NOT deadenylase complex in an mTOR-dependent manner in mesenchymal stem cells, controlling adipogenic commitment and white adipose tissue homeostasis. |
Conditional MSC-specific Imp2 knockout mice, RIP assay, mRNA stability analysis, mTOR pathway inhibition |
Diabetes |
High |
36219823
|
| 2024 |
First small-molecule inhibitors of IGF2BP2/IMP2 were identified and validated: compounds from benzamidobenzoic acid and ureidothiophene classes were confirmed to bind IMP2 by fluorescence polarization assay, thermal shift assay, and saturation-transfer difference NMR, and showed biological activity reducing tumor cell proliferation in vitro and in xenograft models. |
Fluorescence polarization assay, thermal shift assay, saturation-transfer difference NMR, 2D/3D cell culture, zebrafish xenotransplant in vivo |
ACS chemical biology |
High |
35023719
|
| 2022 |
Circ-TNPO3 directly binds IGF2BP2 protein (via RNA pull-down and RIP), and this interaction destabilizes SERPINH1 mRNA, suppressing ccRCC metastasis; rescue experiments confirmed that IGF2BP2/SERPINH1 axis mediates the tumor-suppressive function of circ-TNPO3. |
RNA pull-down, RNA immunoprecipitation, RIP, FISH, rescue assays, in vitro and in vivo models |
Clinical and translational medicine |
Medium |
35876041
|
| 2024 |
IGF2BP2 regulates the stability of GSTM5 mRNA in fibroblast-like synoviocytes, and the IGF2BP2-GSTM5 axis controls inflammatory responses and MMP9/MMP13 expression in rheumatoid arthritis; intra-articular AAV-mediated IGF2BP2 overexpression relieved arthritis in a CIA rat model. |
RNA sequencing, RIP (implied), in vivo CIA rat model with AAV overexpression, mRNA stability assay |
Cell death discovery |
Medium |
38702323
|
| 2021 |
Let-7e-5p directly downregulates Igf2bp2 expression at the mRNA and protein level in C2C12 myotube cells, inhibiting myosin heavy chain expression and impairing mitochondrial function and glucose uptake, causing muscle atrophy. |
microRNA overexpression/knockdown, RT-PCR, western blot in C2C12 myotubes |
Frontiers in endocrinology |
Low |
35002969
|
| 2024 |
circHIPK3 contains an 11-mer motif that constitutes a strong IGF2BP2 binding site; circHIPK3 can nucleate multiple copies of IGF2BP2, potentially via phase separation, to produce IGF2BP2 condensates, sequestering IGF2BP2 as a competing endogenous RNA and regulating STAT3 mRNA stability via IGF2BP2. |
eCLIP dataset mining, RIP assay, absolute copy number quantification, RNA sequencing, phase separation analysis |
eLife |
High |
39041323
|
| 2024 |
High matrix stiffness in pancreatic cancer stabilizes IGF2BP2, which promotes sphingomyelin synthesis via SGMS2 upregulation; this pathway facilitates PD-L1 localization on membrane lipid rafts, enhancing immune evasion. |
MeRIP, RIP, RNA pull-down, single-cell RNA-sequencing, flow cytometry, multiplex IHC, humanized mouse models, PDAC organoids |
Gastroenterology |
High |
40158738
|
| 2024 |
TRIM15 ubiquitinates IGF2BP2, which enhances IGF2BP2's function in phase separation and maintenance of TLR4 mRNA stability in pancreatic cancer; IGF2BP2 combines with TLR4 to inhibit its mRNA degradation. |
Transcriptomics, proteomics, Co-IP, ubiquitination assay, in vivo orthotopic mouse model |
Biochimica et biophysica acta. Molecular basis of disease |
Medium |
38657551
|
| 2024 |
IGF2BP2 directly interacts with CD5L and CD36 mRNA (confirmed by RIP), stabilizing their expression; in osteoclastogenesis during periodontitis, IGF2BP2 regulates osteoclast differentiation via CD36 and CD5L, and its deficiency exacerbates early-stage inflammation but reduces osteoclast differentiation at later stages. |
RIP assay, AAV-mediated knockdown, ligature-induced periodontitis mouse model, overexpression rescue experiments |
Journal of dental research |
Medium |
38193302
|
| 2025 |
A circular RNA (circRNA-BISC) contains a 'CAC-linker-XGGX' motif that specifically binds IGF2BP2 (but not IGF2BP1 or IGF2BP3), inhibiting IGF2BP2-mediated translation enhancement of c-MYC mRNA and overcoming BETi resistance in TNBC. |
RIP-Seq, RNA immunoprecipitation, in vitro transcribed circRNA functional assays, cell and in vivo BETi-resistant TNBC models |
Proceedings of the National Academy of Sciences of the United States of America |
High |
40591591
|
| 2022 |
IGF2BP2 promotes YAP mRNA translation by recognizing its m6A modification in colorectal cancer; YAP subsequently promotes TEAD4 enrichment at the ErbB2 promoter to upregulate ErbB2 expression. |
RIP assay, m6A recognition, promoter enrichment assay |
Cancer science |
Medium |
34309973
|
| 2024 |
IGF2BP2 stabilizes m6A-modified FOSL1 mRNA in trophoblast cells in an IGF2BP2-dependent manner downstream of METTL3; elevated FOSL1 inhibits trophoblast invasion, contributing to fetal growth restriction. |
MeRIP-seq, RNA-seq, RIP assay, mRNA stability assay, in vivo FGR mouse model |
FASEB journal |
Medium |
39565355
|