2. Academic Validation
  3. RBM39 Enhances Cholangiocarcinoma Growth Through EZH2-mediated WNT7B/β-catenin Pathway

RBM39 Enhances Cholangiocarcinoma Growth Through EZH2-mediated WNT7B/β-catenin Pathway

  • Cell Mol Gastroenterol Hepatol. 2024 Sep 14:101404. doi: 10.1016/j.jcmgh.2024.101404.
Nianli Liu 1,  Jinqiang Zhang 2,  Weina Chen 2,  Wenbo Ma 2,  Tong Wu 3
Affiliations

Affiliations

  • 1 Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana; Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
  • 2 Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana.
  • 3 Department of Pathology and Laboratory Medicine, Tulane University School of Medicine, New Orleans, Louisiana. Electronic address: twu@tulane.edu.
PMID: 39278404 DOI: 10.1016/j.jcmgh.2024.101404
Abstract

Background & aims: The RNA-binding motif protein 39 (RBM39) functions as both an RNA-binding protein and a splicing factor in a variety of Cancer types. However, the function of RBM39 in cholangiocarcinoma (CCA) remains undefined. In this study, we aimed to investigate the role of RBM39 in CCA and explore its potential as a therapeutic target.

Methods: The expression of RBM39 in CCA was investigated by analyzing human CCA tumor specimens. CRISPR/Cas9 or shRNA-mediated depletion of RBM39 was performed in vitro and in vivo to document the oncogenic role of RBM39 in CCA. The anti-tumor effect of the RBM39 inhibitor, Indisulam, in combination with the EZH2 Degrader MS177 was assessed in vitro and in vivo.

Results: RBM39 is significantly increased in human CCA tissues and associated with a poor prognosis in patients with CCA. Depletion of RBM39 by CRISPR/Cas9 or shRNA inhibited CCA cell proliferation in vitro and prevented CCA development and tumor growth in mice. Mechanistically, our results showed that depletion of RBM39 suppressed EZH2 expression via disrupting its mRNA splicing. RBM39-regulated EZH2 controls WNT7B/β-catenin activity. Pharmacological co-targeting of RBM39 (with Indisulam) and EZH2 (with MS177) resulted in a synergistic antitumor effect, both in vitro and in vivo.

Conclusion: This study discloses a novel RBM39-EZH2-β-catenin signaling axis that is crucial for CCA growth. Our findings suggest that simultaneous inhibition of RBM39 and EZH2 presents a promising therapeutic strategy for CCA treatment.

Keywords

Cholangiocarcinoma; EZH2; RBM39; WNT7B/β-catenin.

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