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BNIP1 通过 mTOR 抑制宫颈癌细胞的增殖、迁移和侵袭,并促进细胞凋亡。

BNIP1 inhibits cell proliferation, migration and invasion, and promotes apoptosis by mTOR in cervical cancer cells.

机构信息

Department of Oncology, the Second Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Eur Rev Med Pharmacol Sci. 2019 Feb;23(4):1397-1407. doi: 10.26355/eurrev_201902_17096.

Abstract

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.

摘要

目的

BNIP1 是 BH3 仅蛋白家族的一员,在多种生物学过程中发挥着重要作用。然而,BNIP1 在宫颈癌中的作用机制尚不清楚。我们旨在通过 mTOR 信号通路探讨 BNIP1 对宫颈癌细胞增殖、凋亡、迁移和侵袭能力的影响。

患者与方法

采用 qRT-PCR 和 Western blot 检测 BNIP、mTOR 和 p70S6K1 的表达。CCK-8、Transwell 和流式细胞术检测细胞的代表性增殖、迁移、侵袭和凋亡能力。

结果

研究发现 BNIP1 在宫颈癌组织和细胞中呈低表达,且与淋巴转移呈负相关。过表达 BNIP1 抑制了宫颈癌细胞的增殖、迁移和侵袭,促进了细胞凋亡。沉默 BNIP1 则通过 siRNAs 加速了宫颈癌细胞的增殖、迁移和侵袭,抑制了细胞凋亡。此外,我们发现 BNIP1 显著抑制了 mTOR、p70S6K1 和 p-p70S6K1 的表达;BNIP1 通过调节 mTOR 表达影响了宫颈癌细胞的增殖、凋亡、迁移和侵袭能力。

结论

BNIP1 可作为宫颈癌治疗的标志物。

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