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顺铂耐药肝癌细胞中的 miR-106a/b 的水平转移可以改变宫颈癌对顺铂的敏感性。

Horizontal transfer of miR-106a/b from cisplatin resistant hepatocarcinoma cells can alter the sensitivity of cervical cancer cells to cisplatin.

机构信息

Department of Biochemistry and Molecular Biology, Central University of Kerala, Nileshwar, Kasargod, Kerala, India.

Chemical Sciences & Technology Division (CSTD), CSIR-National Institute for Interdisciplinary Science & Technology, (CSIR-NIIST), CSIR, Trivandrum 695019, India.

出版信息

Cell Signal. 2017 Oct;38:146-158. doi: 10.1016/j.cellsig.2017.07.005. Epub 2017 Jul 11.

Abstract

Recent studies indicate that horizontal transfer of genetic material can act as a communication tool between heterogenous populations of tumour cells, thus altering the chemosensitivity of tumour cells. The present study was designed to check whether the horizontal transfer of miRNAs released by cisplatin resistant (Cp-r) Hepatocarcinoma cells can alter the sensitivity of cervical cancer cells. For this exosomes secreted by cisplatin resistant and cisplatin sensitive HepG2 cells (EXres and EXsen) were isolated and characterised. Cytotoxicity analysis showed that EXres can make Hela cells resistant to cisplatin. Analysis of miR-106a/b levels in EXres and EXsen showed that their levels vary. Mechanistic studies showed that miR-106a/b play an important role in EXsen and EXres mediated change in chemosensitivity of Hela cells to cisplatin. Further SIRT1 was identified as a major target of miR-106a/b using in silico tools and this was proved by experimentation. Also the effect of miR-106a/b in chemosensitivity was seen to be dependent on regulation of SIRT1 by miR-106a/b. In brief, this study brings into light, the SIRT1 dependent mechanism of miR-106a/b mediated regulation of chemosensitivity upon the horizontal transfer from one cell type to another.

摘要

最近的研究表明,遗传物质的水平转移可以作为肿瘤细胞异质群体之间的一种通讯工具,从而改变肿瘤细胞的化疗敏感性。本研究旨在检查顺铂耐药(Cp-r)肝癌细胞释放的 miRNAs 是否可以通过水平转移改变宫颈癌(Hela)细胞的敏感性。为此,分离并鉴定了顺铂耐药和顺铂敏感 HepG2 细胞(EXres 和 EXsen)分泌的外泌体。细胞毒性分析表明,EXres 可使 Hela 细胞对顺铂产生耐药性。对 EXres 和 EXsen 中 miR-106a/b 水平的分析表明,其水平存在差异。机制研究表明,miR-106a/b 在 EXsen 和 EXres 介导的 Hela 细胞对顺铂化疗敏感性变化中发挥重要作用。进一步的研究表明,SIRT1 是 miR-106a/b 的主要靶标,这是通过计算机工具预测得到的,并通过实验得到证实。此外,miR-106a/b 在化疗敏感性中的作用似乎依赖于 miR-106a/b 对 SIRT1 的调节。简而言之,本研究揭示了 SIRT1 依赖的机制,即在细胞间水平转移时,miR-106a/b 通过调节 SIRT1 来调节化疗敏感性。

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