Screening and molecular mechanism research on bile microRNAs associated with chemotherapy efficacy in perihilar cholangiocarcinoma

  • iScience. 2024 Dec 4;27(12):111437. doi: 10.1016/j.isci.2024.111437.
Shijie Fu  1 Haizhen Du  2 Yuyang Dai  3 Kanglian Zheng  3 Guang Cao  3 Liang Xu  3 Yujie Zhong  3 Chuanxin Niu  3 Yan Kong  2 Xiaodong Wang  3
Affiliations
  • 1. Department of Interventional Radiology, Beijing Friendship Hospital, Capital Medical University, Beijing 100000, China.
  • 2. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Renal Cancer and Melanoma, Peking University Cancer Hospital and Institute, Beijing 100142, China.
  • 3. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Interventional Oncology, Peking University Cancer Hospital & Institute, Beijing 100142, China.
Abstract

The efficacy of hepatic arterial infusion chemotherapy (HAIC) with oxaliplatin (OXA) and 5-fluorouracil (5-Fu) for treating advanced perihilar cholangiocarcinoma (pCCA) has been demonstrated, yet the survival benefits of HAIC for pCCA patients vary. Here, we aimed to screen out HAIC resistance-related bile MicroRNAs (miRNAs) and explore the functions of specific bile miRNAs in pCCA based on high-throughput Sequencing. Levels of bile miR-532-3p, miR-1250-5p, and miR-4772-5p were related to the survival of advanced pCCA patients after HAIC. However, only overexpression of miR-532-3p promoted OXA/5-Fu resistance, and downregulation of its expression improved sensitivity to OXA/5-Fu. Mechanistic investigations revealed secreted protein acidic and rich in cysteine (SPARC) as the direct target of miR-532-3p. Our study reveals that bile miR-532-3p, miR-1250-5p, and miR-4772-5p may serve as survival biomarkers in advanced pCCA patients after HAIC and that bile miR-532-3p promotes resistance to HAIC with OXA and 5-Fu via negatively regulating SPARC expression.

Keywords
Cancer; Cell biology; Molecular biology.
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