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MicroRNA-195 调控卵巢癌细胞中 MICU1 的表达和肿瘤生长。

MicroRNA-195 controls MICU1 expression and tumor growth in ovarian cancer.

机构信息

Department of Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

Department of Obstetrics and Gynecology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, USA.

出版信息

EMBO Rep. 2020 Oct 5;21(10):e48483. doi: 10.15252/embr.201948483. Epub 2020 Aug 27.

Abstract

MICU1 is a mitochondrial inner membrane protein that inhibits mitochondrial calcium entry; elevated MICU1 expression is characteristic of many cancers, including ovarian cancer. MICU1 induces both glycolysis and chemoresistance and is associated with poor clinical outcomes. However, there are currently no available interventions to normalize aberrant MICU1 expression. Here, we demonstrate that microRNA-195-5p (miR-195) directly targets the 3' UTR of the MICU1 mRNA and represses MICU1 expression. Additionally, miR-195 is under-expressed in ovarian cancer cell lines, and restoring miR-195 expression reestablishes native MICU1 levels and the associated phenotypes. Stable expression of miR-195 in a human xenograft model of ovarian cancer significantly reduces tumor growth, increases tumor doubling times, and enhances overall survival. In conclusion, miR-195 controls MICU1 levels in ovarian cancer and could be exploited to normalize aberrant MICU1 expression, thus reversing both glycolysis and chemoresistance and consequently improving patient outcomes.

摘要

MICU1 是一种位于线粒体内膜的蛋白,能够抑制线粒体钙离子内流;在许多癌症中,包括卵巢癌,MICU1 的表达水平升高。MICU1 可诱导糖酵解和化疗耐药,并与不良的临床预后相关。然而,目前尚无可用的干预措施来使异常的 MICU1 表达正常化。在这里,我们证明 microRNA-195-5p(miR-195)可直接靶向 MICU1 mRNA 的 3'UTR,并抑制 MICU1 的表达。此外,miR-195 在卵巢癌细胞系中表达下调,恢复 miR-195 的表达可恢复天然的 MICU1 水平和相关表型。miR-195 在卵巢癌的人源异种移植模型中的稳定表达可显著降低肿瘤生长,增加肿瘤倍增时间,并提高整体存活率。总之,miR-195 可控制卵巢癌中的 MICU1 水平,并可被利用来使异常的 MICU1 表达正常化,从而逆转糖酵解和化疗耐药,并因此改善患者的预后。

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