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GENE:

GIGYF2 (GRB10 Interacting GYF Protein 2)

i
Other names: GRB10 Interacting GYF Protein 2, PERQ Amino Acid-Rich With GYF Domain-Containing Protein 2, Parkinson Disease (Autosomal Recessive, Early Onset) 11, Trinucleotide Repeat-Containing Gene 15 Protein, PERQ Amino Acid Rich, With GYF Domain 3, GRB10-Interacting GYF Protein 2, TNRC15, PERQ2, GYF2, PERQ Amino Acid Rich, With GYF Domain 2, Trinucleotide Repeat Containing 15, GYF Domain Containing 2, PARK11, GIGYF2, PERQ3
Associations
Trials
4ms
RNA-binding protein GIGYF2 promotes colorectal cancer progression through activation of the METTL3/SERP1/STAT3 axis in an m6A-IGF2BP2-dependent manner. (PubMed, Biochem Pharmacol)
In conclusion, our findings reveal a novel oncogenic pathway driven by GIGYF2, which activates the METTL3/SERP1/STAT3 axis in an m6A-IGF2BP2-dependent manner to enhance the proliferation and migration of cancer cells, contributing to CRC progression. This study may provide a potential prognostic marker and therapeutic target for CRC.
Journal
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GIGYF2 (GRB10 Interacting GYF Protein 2) • IGF2BP2 (Insulin Like Growth Factor 2 MRNA Binding Protein 2) • METTL3 (Methyltransferase Like 3)
over1year
Ribosome Quality Control mitigates the cytotoxicity of ribosome collisions induced by 5-Fluorouracil. (PubMed, Nucleic Acids Res)
Furthermore, 5FU treatment enhances the expression of the key RQC factors ZNF598 and GIGYF2 via an mTOR-dependent post-translational mechanism. This adaptation likely mitigates the cytotoxic consequences of increased ribosome collisions upon 5FU treatment.
Journal
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TYMS (Thymidylate Synthetase) • GIGYF2 (GRB10 Interacting GYF Protein 2)
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GIGYF2 overexpression
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5-fluorouracil
over1year
RNA-binding protein GIGYF2 orchestrates hepatic insulin resistance through STAU1/PTEN-mediated disruption of the PI3K/AKT signaling cascade. (PubMed, Mol Med)
Our study discloses that GIGYF2 mediates obesity-related IR by disrupting the PI3K/AKT signaling axis through the up-regulation of STAU1/PTEN. Targeting GIGYF2 may offer a potential strategy for treating obesity-related metabolic diseases, including type 2 diabetes.
Journal
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PTEN (Phosphatase and tensin homolog) • GIGYF2 (GRB10 Interacting GYF Protein 2)
almost2years
Comprehensive DNA methylation profiling by MeDIP-NGS identifies potential genes and pathways for epithelial ovarian cancer. (PubMed, J Ovarian Res)
POLR3B and GIGYF2 turned out to be the novel genes associated with the carcinogenesis of EOC. Our study demonstrated that methylation profiling through MeDIP-sequencing has effectively identified six potential hub genes and pathways that might exacerbate our understanding of underlying molecular mechanisms of ovarian carcinogenesis.
Journal • Next-generation sequencing • Epigenetic controller
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CRKL (CRK Like Proto-Oncogene, Adaptor Protein) • GIGYF2 (GRB10 Interacting GYF Protein 2) • BMP2 (Bone Morphogenetic Protein 2)
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GIGYF2 overexpression
almost3years
Comprehensive genomic characterization of early-stage bladder cancer from 438 patients by whole genome- and exome sequencing (AACR 2023)
Here we investigated the landscape of DNA alterations in NMIBC in a large patient cohort of NMIBC samples with paired transcriptomic data and detailed clinical follow-up. We identified several novel genomic alterations; specifically, we showed that 15% of the tumors had genome doublings, and we identified a complex underlying copy number landscape of the region containing FGFR3.
Clinical • Tumor mutational burden
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HER-2 (Human epidermal growth factor receptor 2) • TP53 (Tumor protein P53) • TMB (Tumor Mutational Burden) • FGFR3 (Fibroblast growth factor receptor 3) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • RB1 (RB Transcriptional Corepressor 1) • CCND1 (Cyclin D1) • KMT2D (Lysine Methyltransferase 2D) • CDKN2B (Cyclin Dependent Kinase Inhibitor 2B) • ERCC2 (Excision repair cross-complementation group 2) • KMT2C (Lysine Methyltransferase 2C) • KDM6A (Lysine Demethylase 6A) • STAG2 (Stromal Antigen 2) • EP300 (E1A binding protein p300) • GIGYF2 (GRB10 Interacting GYF Protein 2)
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TP53 mutation • HER-2 mutation • CDKN2A deletion • KMT2D mutation • RB1 mutation • CCND1 amplification • KDM6A mutation • EP300 mutation • GIGYF2 overexpression