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miR-34 家族与癌症和细胞凋亡

The miR-34 family in cancer and apoptosis.

机构信息

Experimental and Molecular Pathology, Institute of Pathology, Ludwig-Maximilians-University Munich, Thalkirchner Str. 36, D-80337 Munich, Germany.

出版信息

Cell Death Differ. 2010 Feb;17(2):193-9. doi: 10.1038/cdd.2009.56. Epub 2009 May 22.

Abstract

Recently, the transcription factor encoded by tumor suppressor gene p53 was shown to regulate the expression of microRNAs. The most significant induction by p53 was observed for the microRNAs miR-34a and miR-34b/c, which turned out to be direct p53 target genes. Ectopic miR-34 expression induces apoptosis, cell-cycle arrest or senescence. In many tumor types the promoters of the miR-34a and the miR-34b/c genes are subject to inactivation by CpG methylation. MiR-34a resides on 1p36 and is commonly deleted in neuroblastomas. Furthermore, the loss of miR-34 expression has been linked to resistance against apoptosis induced by p53 activating agents used in chemotherapy. In this review, the evidence for a role of miR-34a and miR-34b/c in the apoptotic response of normal and tumor cells is surveyed.

摘要

最近,肿瘤抑制基因 p53 编码的转录因子被证明可以调节 microRNAs 的表达。p53 最显著的诱导作用发生在 microRNAs miR-34a 和 miR-34b/c 上,它们被证明是 p53 的直接靶基因。异位 miR-34 表达诱导细胞凋亡、细胞周期停滞或衰老。在许多肿瘤类型中,miR-34a 和 miR-34b/c 基因的启动子因 CpG 甲基化而失活。miR-34a 位于 1p36 上,在神经母细胞瘤中通常缺失。此外,miR-34 表达的丧失与化疗中使用的 p53 激活剂诱导的细胞凋亡抵抗有关。在这篇综述中,调查了 miR-34a 和 miR-34b/c 在正常和肿瘤细胞凋亡反应中的作用证据。

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