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首页> 外文期刊>European review for medical and pharmacological sciences. >BNIP1 inhibits cell proliferation, migration and invasion, and promotes apoptosis by mTOR in cervical cancer cells
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BNIP1 inhibits cell proliferation, migration and invasion, and promotes apoptosis by mTOR in cervical cancer cells

机译:BNIP1抑制子宫颈癌细胞中的细胞增殖,迁移和侵袭,并通过mTOR促进其凋亡

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OBJECTIVE: BNIP1, a member of the BH3‐only protein family, plays essential roles in a variety of biological processes. However, the mechanism and function of BNIP1 are still unknown in cervical cancer. We aim to explore the roles of BNIP1 on cervical cancer cell proliferation, apoptosis, migration, and invasion abilities by mTOR signaling pathway. PATIENTS AND METHODS: qRT-PCR and Western blot assays were performed to assess BNIP, mTOR, and p70S6K1 expressions. CCK-8, transwell and flow cytometry assays were used to measure the representative proliferation, migration, invasion, and apoptosis abilities. RESULTS: Our findings indicated that BNIP1 is down-expressed in cervical cancer tissues and cells, and was negatively associated with lymphatic metastasis. Overexpression of BNIP1 suppressed proliferation, migration and invasion, and promoted apoptosis of cervical cancer cells. Silence of BNIP1 by siRNAs accelerated proliferation, migration and invasion, and inhibited apoptosis of cervical cancer cells. In addition, we found that BNIP1 significantly inhibited mTOR, p70S6K1, and p-p70S6K1 expressions; BNIP1 affected the proliferation, apoptosis, migration, and invasion abilities of cervical cancer cells by regulating mTOR expression. CONCLUSIONS: BNIP1 can be considered a marker for cervical carcinoma therapy.
机译:目的:BNIP1,仅BH3蛋白家族的成员,在各种生物学过程中都起着至关重要的作用。然而,BNIP1的机制和功能在宫颈癌中仍然未知。我们旨在通过mTOR信号通路探索BNIP1在宫颈癌细胞增殖,凋亡,迁移和侵袭能力中的作用。病人和方法:进行qRT-PCR和Western blot分析以评估BNIP,mTOR和p70S6K1的表达。使用CCK-8,transwell和流式细胞仪测定来测量代表性的增殖,迁移,侵袭和凋亡能力。结果:我们的研究结果表明BNIP1在宫颈癌组织和细胞中低表达,并与淋巴结转移负相关。 BNIP1的过表达抑制宫颈癌细胞的增殖,迁移和侵袭,并促进其凋亡。 siRNA沉默BNIP1可加速子宫颈癌细胞的增殖,迁移和侵袭,并抑制其凋亡。此外,我们发现BNIP1显着抑制了mTOR,p70S6K1和p-p70S6K1的表达。 BNIP1通过调节mTOR表达影响子宫颈癌细胞的增殖,凋亡,迁移和侵袭能力。结论:BNIP1可被认为是宫颈癌治疗的标志物。

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