IGF2BP1-mediated N6-methyladenosine modification promotes intrahepatic cholangiocarcinoma progression

N6-methyladenosine (m6A) RNA methylation and its associated RNA-binding protein insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) are involved in tumor initiation and progression. Here, we explored the biological function and clinical significance of IGF2BP1 in intrahepatic cholangiocarcinoma (iCCA). We found that IGF2BP1 expression was upregulated by H3K27 acetylation enrichment of its promoter, which positively correlated with poor clinicopathological characteristics and survival. Gain-and loss-of-function experiments showed that IGF2BP1 overexpression (knockdown) enhanced (attenuated) iCCA growth and metastasis in vitro and in vivo. Mechanistically, IGF2BP1 not only regulated the c-Myc/p16 axis to promote iCCA growth and inhibit senescence, but also activated the ZIC2/PAK4/AKT/MMP2 axis to induce tumor metastasis. More importantly, BTYNB, a recently identified IGF2BP1 inhibitor, exerted promising anti-tumor efficacy in a patient-derived xenograft (PDX) model, and IGF2BP1 conditional knockout (cKO) reduced the tumor burden. These results demonstrate the crucial role of IGF2BP1 in iCCA progression via m6A-dependent modification, highlighting IGF2BP1 as a potential therapeutic target in iCCA.

Automated summary

IGF2BP1 plays a crucial role in the initiation and progression of intrahepatic cholangiocarcinoma (iCCA) through its regulation of the c-Myc/p16 and ZIC2/PAK4/AKT/MMP2 signaling pathways. Upregulation of IGF2BP1 is associated with poor clinicopathological characteristics and survival. Inhibition of IGF2BP1 using the inhibitor BTYNB shows promising anti-tumor efficacy in a patient-derived xenograft (PDX) model.