Suppr超能文献

p53 通过诱导 LIMA1/EPLIN 抑制癌细胞侵袭。

p53 mediates the suppression of cancer cell invasion by inducing LIMA1/EPLIN.

机构信息

Department of Medical Genome Sciences, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Japan; Research Fellow of Japan Society for the Promotion of Science, Japan.

Department of Medical Genome Sciences, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Japan.

出版信息

Cancer Lett. 2017 Apr 1;390:58-66. doi: 10.1016/j.canlet.2016.12.034. Epub 2017 Jan 13.

Abstract

The tumor suppressor gene p53 is frequently mutated in human cancer. p53 executes various functions, such as apoptosis induction and cell cycle arrest, by modulating transcriptional regulation. In this study, LIM domain and Actin-binding protein 1 (LIMA1) was identified as a target of the p53 family using a cDNA microarray. We also evaluated genome-wide occupancy of the p53 protein by performing chromatin immunoprecipitation-sequencing (ChIP-seq) and identified two p53 response elements in the LIMA1 gene. LIMA1 protein levels were increased by treatment with nutlin-3a, a small molecule that activates endogenous p53. In addition, LIMA1 expression was significantly downregulated in cancers compared with normal tissues. Knockdown of LIMA1 significantly enhanced cancer cell invasion and partially inhibited p53-induced suppression of cell invasion. Furthermore, low expression of LIMA1 in cancer patients correlated with decreased survival and poor prognosis. Thus, p53-induced LIMA1 inhibits cell invasion, and the downregulation of LIMA1 caused by p53 mutation results in decreased survival in cancer patients. Collectively, this study reveals the molecular mechanism of LIMA1 downregulation in various cancers and suggests that LIMA1 may be a novel prognostic predictor and a therapeutic target for cancer.

摘要

抑癌基因 p53 在人类癌症中经常发生突变。p53 通过调节转录调控来执行多种功能,如诱导细胞凋亡和细胞周期停滞。在这项研究中,我们使用 cDNA 微阵列鉴定出 LIM 结构域和肌动蛋白结合蛋白 1(LIMA1)是 p53 家族的一个靶标。我们还通过染色质免疫沉淀测序(ChIP-seq)评估了 p53 蛋白的全基因组结合情况,并在 LIMA1 基因中鉴定出两个 p53 反应元件。用激活内源性 p53 的小分子 nutlin-3a 处理后,LIMA1 蛋白水平增加。此外,与正常组织相比,癌症中 LIMA1 的表达显著下调。LIMA1 的敲低显著增强了癌细胞的侵袭,部分抑制了 p53 诱导的细胞侵袭抑制。此外,癌症患者中 LIMA1 的低表达与降低的存活率和不良预后相关。因此,p53 诱导的 LIMA1 抑制细胞侵袭,而 p53 突变导致的 LIMA1 下调导致癌症患者存活率降低。总之,这项研究揭示了 LIMA1 在各种癌症中下调的分子机制,并表明 LIMA1 可能是癌症的一个新的预后预测因子和治疗靶点。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验