ROBO1 p.E280* Loses the Inhibitory Effects on the Proliferation and Angiogenesis of Wild-Type ROBO1 in Cholangiocarcinoma by Interrupting SLIT2 Signal

Tao Zhou; Yaodong Zhang; Yananlan Chen; Jijun Shan; Jifei Wang; Yirui Wang; Jiang Chang; Wangjie Jiang; Ruixiang Chen; Ziyi Wang; Xiaoli Shi; Yue Yu; Changxian Li; Xiangcheng Li

doi:10.3389/fonc.2022.879963

ROBO1 p.E280* Loses the Inhibitory Effects on the Proliferation and Angiogenesis of Wild-Type ROBO1 in Cholangiocarcinoma by Interrupting SLIT2 Signal

Front Oncol. 2022 May 9:12:879963. doi: 10.3389/fonc.2022.879963. eCollection 2022.

Authors

Tao Zhou¹, Yaodong Zhang¹, Yananlan Chen¹, Jijun Shan¹, Jifei Wang¹, Yirui Wang¹, Jiang Chang¹, Wangjie Jiang¹, Ruixiang Chen¹, Ziyi Wang¹, Xiaoli Shi¹, Yue Yu^{1

2}, Changxian Li^{1

2}, Xiangcheng Li^{1

2}

Affiliations

¹ Hepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
² Key Laboratory of Liver Transplantation, Chinese Academy of Medical Sciences, National Health Commission (NHC) Key Laboratory of Liver Transplantation, Nanjing, China.

Abstract

Background: Cholangiocarcinoma (CCA) remains one of the most lethal malignancies with an increasing incidence globally. Through whole-exome sequencing of 67 CCA tissues, we identified new mutated genes in CCA, including MACF1, METTL14, ROBO1, and so on. The study was designed to explore the effects and mechanism of ROBO1 wild type (ROBO1^WT) and ROBO1^E280* mutation on the progression of CCA.

Methods: Whole-exome sequencing was performed to identify novel mutations in CCAs. In vitro and in vivo experiments were used to examine the function and mechanism of ROBO1^WT and ROBO1^E280* in cholangiocarcinoma. A tissue microarray including 190 CCA patients and subsequent analyses were performed to indicate the clinical significance of ROBO1.

Results: Through whole-exome sequencing, we identified a novel CCA-related mutation, ROBO1^E280*. ROBO1 was downregulated in CCA tissues, and the downregulation of ROBO1 was significantly correlated with poor prognosis. ROBO1^WT suppressed the proliferation and angiogenesis of CCA in vitro and in vivo, while ROBO1^E280* lost the inhibitory effects. Mechanically, ROBO1^E280* translocated from the cytomembrane to the cytoplasm and interrupted the interaction between SLIT2 and ROBO1. We identified OLFML3 as a potential target of ROBO1 by conducting RNA-Seq assays. OLFML3 expression was downregulated by ROBO1^WT and recovered by ROBO1^E280*. Functionally, the silence of OLFML3 inhibited CCA proliferation and angiogenesis and was sufficient to repress the loss-of-function role of ROBO1^E280*.

Conclusions: These results suggest that ROBO1 may act as a tumor suppressor and potential prognostic marker for CCA. ROBO1^E280* mutation is a loss-of-function mutation, and it might serve as a candidate therapeutic target for CCA patients.

Keywords: ROBO1; angiogenesis; cholangiocarcinoma; nonsense mutation; proliferation.