Basic & Clinical Medicine ›› 2025, Vol. 45 ›› Issue (8): 1066-1072.doi: 10.16352/j.issn.1001-6325.2025.08.1066

• Original Articles • Previous Articles     Next Articles

RPRD1B is highly expressed in human ovarian cancer cell lines and promotes tumor cell proliferation

TIAN Ye1,2, HE Quan1,2, WANG Xiaojuan3*   

  1. 1. Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, Beijing 102218;
    2. Institute for Organ Transplant and Bionic Medicine, Tsinghua University, Beijing 102218;
    3. Hepatobiliary Pancreatic Center, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, Beijing 102218, China
  • Received:2025-04-23 Revised:2025-06-10 Online:2025-08-05 Published:2025-07-11
  • Contact: *wxj0250@163.com

Abstract: Objective To explore the role of regulation of nuclear pre-mRNA-domain-containing 1B(RPRD1B)in human ovarian cancer. Methods The expression level of RPRD1B in ovarian cancer was detected by RT-qPCR and Western blot experiments. Based on the CRISPR/Cas9 system and lentiviral system, the A2780 and SKOV3 cell lines with RPRD1B gene knockout and over-expression were respectively constructed, and their functions in ovarian cancer were verified by wound-healing assay, Transwell assay and mouse subcutaneous tumor formation model. Results RPRD1B was highly expressed in ovarian cancer cell lines (P<0.001). Knockout of RPRD1B inhibited the colony formation and proliferation ability of ovarian cancer cells (P<0.001), as well as the cell migration (P<0.05) and invasion ability (P<0.001). Meanwhile, knockout of RPRD1B inhibited the tumorigenesis ability of SKOV3 ovarian cancer cell lines in vivo (P<0.001). Conclusions RPRD1B is highly expressed in human ovarian cancer cell lines and promotes the growth of subcutaneous tumors in mice.

Key words: regulation of nuclear pre-mRNA-domain-containing 1B (RPRD1B), ovarian cancer, proliferation

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