FXR splicing by SF3B3 promotes MYC-driven hepatocarcinogenesis

SF3B3 is a key downstream effector of MYC -driven hepatocarcinogenesis and a critical regulator of FXR splicing. Both SF3B3 and FXR represent druggable vulnerabilities in MYC -amplified HCC.

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Publication Details

Journal
Hepatology
Published
2025-09-23
DOI
https://doi.org/10.1097/hep.0000000000001523
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

FXR splicing by SF3B3 promotes MYC-driven hepatocarcinogenesis

Haichuan Wang, Jiahua Luo, Xichuan Li, Lifeng Han et al.
1 citations
Hepatology
RNA and protein synthesis mechanisms
0.81
article

FXR splicing by SF3B3 promotes MYC-driven hepatocarcinogenesis

Haichuan Wang, Jiahua Luo, Xichuan Li, Lifeng Han, Gen Li, Weihua Zhang, Xue Chao Wang, Ming Zhang, Tong Xu, Youcai Zhang
article en
1 citations

Abstract

SF3B3 is a key downstream effector of MYC -driven hepatocarcinogenesis and a critical regulator of FXR splicing. Both SF3B3 and FXR represent druggable vulnerabilities in MYC -amplified HCC.

Hepatology
Tianjin University of Traditional Chinese Medicine (CN), Tianjin Normal University (CN), Sichuan University (CN), West China Hospital of Sichuan University (CN), Cancer Center of Hawaii (US), Tianjin haihe hospital (CN)
Openalex Percentile: Top 23%
RNA and protein synthesis mechanisms
0.81
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FXR splicing by SF3B3 promotes MYC-driven hepatocarcinogenesis — Haichuan Wang, Jiahua Luo, et al. · Hepatology (2025) | TGRS Research Map | TGRS