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miR-596 通过调节细胞存活和死亡来调控黑色素瘤生长。

miR-596 Modulates Melanoma Growth by Regulating Cell Survival and Death.

机构信息

Department of Biomedical Sciences and Engineering, College of Health Sciences and Technology, National Central University, Taoyuan, Taiwan.

Genomics Research Center, Academia Sinica, Taipei, Taiwan.

出版信息

J Invest Dermatol. 2018 Apr;138(4):911-921. doi: 10.1016/j.jid.2017.11.016. Epub 2017 Nov 26.

Abstract

Tumors grow because cancer cells lack the ability to balance cell survival and death signaling pathways. miR-596, a microRNA located at the 8p23.3 locus, has been shown by the TCGA-Assembler to be deleted in a significant number of melanoma samples. Here, we also validated the low levels of miR-596 in melanoma compared to tissue nevi, and Kaplan-Meier curve analysis revealed that low miR-596 expression was associated with worse overall survival. Moreover, we showed that miR-596 overexpression effectively inhibited MAPK/ERK signaling, cell proliferation, migration, and invasion and increased the cell apoptosis of melanoma cells. In addition, we found that miR-596 directly targets MEK1 and two apoptotic proteins, MCL1, and BCL2L1, in melanoma cells. Our findings indicated that miR-596 is an important miRNA that both negatively regulates the MAPK/ERK signaling pathway by targeting MEK1 and modulates the apoptosis pathway by targeting MCL1 and BCL2L1, suggesting that miR-596 could be a therapeutic candidate for treating melanoma, and a prognostic factor for melanoma patients.

摘要

肿瘤之所以生长,是因为癌细胞缺乏平衡细胞存活和死亡信号通路的能力。miR-596 是位于 8p23.3 位置的 microRNA,TCGA-Assembler 已经证实其在大量黑色素瘤样本中缺失。在这里,我们还验证了与组织痣相比,黑色素瘤中 miR-596 的水平较低,Kaplan-Meier 曲线分析表明低表达 miR-596 与总生存期较差相关。此外,我们表明 miR-596 的过表达有效地抑制了 MAPK/ERK 信号、细胞增殖、迁移和侵袭,并增加了黑色素瘤细胞的细胞凋亡。此外,我们发现 miR-596 在黑色素瘤细胞中直接靶向 MEK1 和两种凋亡蛋白 MCL1 和 BCL2L1。我们的研究结果表明,miR-596 是一种重要的 miRNA,通过靶向 MEK1 负调控 MAPK/ERK 信号通路,并通过靶向 MCL1 和 BCL2L1 调节凋亡通路,表明 miR-596 可能成为治疗黑色素瘤的治疗候选物,也是黑色素瘤患者的预后因素。

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