医学新知2026，Vol.36Issue(1)：62-69,8.DOI:10.12173/j.issn.1004-5511.202505149
SOX9通过调控SLC7A11/GPX4介导的铁死亡抑制卵巢癌进展的机制研究
SOX9 promotes ovarian cancer progression through activating ferroptosis via SLC7A11/GPX4 pathway
摘要
Abstract
Objective To investigate the role and mechanism of sex-determining region Y-box protein 9(SOX9)in the progression of ovarian cancer.Methods The ovarian cancer cell lines with stable knockdown of SOX9 were constructed.The effects of SOX9 knockdown on the proliferation,invasion and migration abilities of ovarian cancer cell lines were detected by CCK-8 assay,Transwell assay,and cell scratch assay,respectively.The effects of SOX9 knockdown on ferroptosis in ovarian cancer cell lines were evaluated by the level of Fe2+,glutathione(GSH),malondialdehyde(MDA),and Western blot analysis.The effects of SOX9 knockdown on the lipid peroxidation level of ovarian cancer cell lines were observed by confocal fluorescence microscopy.Chromatin immunoprecipitation followed by quantitative PCR(ChIP-qPCR)was performed to examine the binding of SOX9 to its downstream target gene,SLC7A11.Results Knockdown of SOX9 significantly inhibits the proliferation,invasion and migration abilities of ovarian cancer cells.Meanwhile,SOX9 transcriptionally regulates SLC7A11 and activates ferroptosis via the SLC7A11/GPX4 signaling axis.Conclusion SOX9 promotes ferroptosis in ovarian cancer cells by regulating the SLC7A11/GPX4 signaling pathway,ultimately inhibiting ovarian cancer progression.关键词
SOX9/卵巢癌/铁死亡Key words
SOX9/Ovarian cancer/Ferroptosis分类
医药卫生引用本文复制引用
叶学均,王中显,李贵香,程大玲,陶杏元..SOX9通过调控SLC7A11/GPX4介导的铁死亡抑制卵巢癌进展的机制研究[J].医学新知,2026,36(1):62-69,8.基金项目
湖北省自然科学基金(2021CFB576) （2021CFB576）
