ATP6V1B1 通过 mTOR/autophagy 通路调控卵巢癌的进展和顺铂敏感性。

IF 3.5 2区 生物学 Q3 CELL BIOLOGY Molecular and Cellular Biochemistry Pub Date : 2025-02-01 Epub Date: 2024-05-12 DOI:10.1007/s11010-024-05025-w
Shien Mo, Tingji Liu, Haiqin Zhou, Junning Huang, Ling Zhao, Fangfang Lu, Yan Kuang
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引用次数: 0

摘要

卵巢癌是一种严重的妇科恶性肿瘤,其早期发现和有效化疗需要进一步的进展。本研究旨在探讨 ATPase H+-Transporting V1 Subunit B1(ATP6V1B1)在卵巢癌发生和化疗耐药中的分子机制。我们的数据显示,ATP6V1B1在卵巢癌中上调,并与无进展生存期下降相关。功能增益和功能缺失实验表明,ATP6V1B1 在体外促进卵巢癌细胞的增殖、迁移和侵袭,而 ATP6V1B1 基因敲除在体内抑制肿瘤生长。此外,敲除 ATP6V1B1 会增加卵巢癌细胞对顺铂的敏感性。机理研究表明,ATP6V1B1调节mTOR/自噬通路的激活。总之,我们的研究证实了ATP6V1B1在卵巢癌中的致癌作用,并揭示了ATP6V1B1通过mTOR/自噬轴促进卵巢癌的进展。
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ATP6V1B1 regulates ovarian cancer progression and cisplatin sensitivity through the mTOR/autophagy pathway.

Early detection and effective chemotherapy for ovarian cancer, a serious gynecological malignancy, require further progress. This study aimed to investigate the molecular mechanism of ATPase H+-Transporting V1 Subunit B1 (ATP6V1B1) in ovarian cancer development and chemoresistance. Our data show that ATP6V1B1 is upregulated in ovarian cancer and correlated with decreased progression-free survival. Gain- and loss-of-function experiments demonstrated that ATP6V1B1 promotes the proliferation, migration, and invasion of ovarian cancer cells in vitro, while ATP6V1B1 knockout inhibits tumor growth in vivo. In addition, knocking down ATP6V1B1 increases the sensitivity of ovarian cancer cells to cisplatin. Mechanistic studies showed that ATP6V1B1 regulates the activation of the mTOR/autophagy pathway. Overall, our study confirmed the oncogenic role of ATP6V1B1 in ovarian cancer and revealed that ATP6V1B1 promotes ovarian cancer progression via the mTOR/autophagy axis.

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来源期刊
Molecular and Cellular Biochemistry
Molecular and Cellular Biochemistry 生物-细胞生物学
CiteScore
8.30
自引率
2.30%
发文量
293
审稿时长
1.7 months
期刊介绍: Molecular and Cellular Biochemistry: An International Journal for Chemical Biology in Health and Disease publishes original research papers and short communications in all areas of the biochemical sciences, emphasizing novel findings relevant to the biochemical basis of cellular function and disease processes, as well as the mechanics of action of hormones and chemical agents. Coverage includes membrane transport, receptor mechanism, immune response, secretory processes, and cytoskeletal function, as well as biochemical structure-function relationships in the cell. In addition to the reports of original research, the journal publishes state of the art reviews. Specific subjects covered by Molecular and Cellular Biochemistry include cellular metabolism, cellular pathophysiology, enzymology, ion transport, lipid biochemistry, membrane biochemistry, molecular biology, nuclear structure and function, and protein chemistry.
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