Chen Qingqing, Ouyang Ling
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Cell Signal. 2025 Oct;134:111910. doi: 10.1016/j.cellsig.2025.111910. Epub 2025 May 28.
Recent findings have indicated that the F-box E3 ubiquitin ligase, F-box only protein 11 (FBXO11), may serve a tumor-suppressing role in certain types of cancers. However, its specific function in ovarian cancer (OC) remains to be elucidated. This study revealed that FBXO11 expression is reduced in OC tissues compared to normal tissues. To assess the role of FBXO11 in OC cells, we established stable human OC cell lines with tetracycline-inducible (Tet-on) expression of FBXO11 CDS or shRNA. FBXO11 inhibited OC cell proliferation, colony formation, migration, invasion, and cell cycle transition from G0/G1 to S phase in vitro. Moreover, FBXO11 suppressed xenograft tumor growth in mice in vivo. Concurrently, FBXO11 reduced the volume of ascites and the number of metastatic tumor nodules in the peritoneal metastasis model. Mechanistically, FBXO11 promoted kinesin family member 2C (KIF2C) to undergo K48-linked ubiquitination and proteasomal degradation, and KIF2C knockdown reversed the tumor-promoting function of FBXO11 downregulation. Additionally, we demonstrated that FBXO11 is a transcriptional target of zinc-finger protein 217 (ZNF217), a known transcriptional repressor that has been implicated in the promotion of OC progression and the prediction of poor prognosis. In summary, FBXO11 functions as a tumor suppressor in OC through ubiquitin-proteasomal degradation of KIF2C; and the low expression level of FBXO11 in OC may be attributed to its transcriptional inhibition by transcription factor ZNF217. These findings provided new insights into understanding the molecular mechanism of OC progression.
最近的研究结果表明,F-box E3泛素连接酶,仅含F-box蛋白11(FBXO11),可能在某些类型的癌症中发挥肿瘤抑制作用。然而,其在卵巢癌(OC)中的具体功能仍有待阐明。本研究发现,与正常组织相比,OC组织中FBXO11的表达降低。为了评估FBXO11在OC细胞中的作用,我们建立了稳定的人OC细胞系,其FBXO11 CDS或shRNA可通过四环素诱导(Tet-on)表达。FBXO11在体外抑制OC细胞增殖、集落形成、迁移、侵袭以及从G0/G1期到S期的细胞周期转变。此外,FBXO11在体内抑制小鼠异种移植瘤的生长。同时,在腹膜转移模型中,FBXO11减少了腹水的体积和转移瘤结节的数量。机制上,FBXO11促进驱动蛋白家族成员2C(KIF2C)发生K48连接的泛素化和蛋白酶体降解,而敲低KIF2C可逆转FBXO11下调的促肿瘤功能。此外,我们证明FBXO11是锌指蛋白217(ZNF217)的转录靶点,ZNF217是一种已知的转录抑制因子,与OC进展的促进和不良预后的预测有关。总之,FBXO11通过对KIF2C进行泛素-蛋白酶体降解在OC中发挥肿瘤抑制作用;OC中FBXO11的低表达水平可能归因于转录因子ZNF217对其转录的抑制。这些发现为理解OC进展的分子机制提供了新的见解。