结肠癌转移相关蛋白1 (MACC1)在癌症中的潜在治疗应用和预后意义

E. Kopczynska
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引用次数: 19

摘要

结肠癌转移相关基因1 (MACC1)于2009年被发现。与正常组织或腺瘤相比,MACC1在原发性和转移性结肠癌中的表达明显上调。MACC1的诱导发生在从良性表型向恶性表型转变的关键步骤。本综述的目的是总结目前关于MACC1在癌症发生和进展中的作用的非临床和临床研究的结果,以及其潜在的治疗和预后意义。编码HGF受体MET的基因是MACC1的转录靶点。除了在细胞培养中促进结肠癌细胞的增殖、侵袭和迁移以及小鼠模型中肿瘤的生长和转移外,MACC1还通过β-catenin信号通路和间充质-上皮转化参与结直肠癌的癌变和进展。用si/sh RNA敲低MACC1在不同类型肿瘤细胞系中进行了研究。MACC1是癌症抗肿瘤和抗转移干预策略的一个有希望的治疗靶点。在这里,它被认为是一个潜在的独立的预后指标,降低了总生存和远处转移的发生在不同类型的癌症患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The potential therapeutic applications and prognostic significance of metastasis-associated in colon cancer-1 (MACC1) in cancers
The metastasis-associated in colon cancer-1 (MACC1) gene was identified in 2009. Expression of MACC1 was found to be significantly upregulated in primary and metastatic colon carcinomas compared to normal tissues or adenomas. The induction of MACC1 occurs at the crucial step of transition from a benign to a malignant phenotype. The aim of this review was to summarise current results of non-clinical and clinical studies on the role of MACC1 in the carcinogenesis and progression of cancer, as well its potential therapeutic and prognostic significance. The gene encoding the HGF receptor MET is a transcriptional target of MACC1. In addition to promoting the proliferation, invasion, and migration of colon cancer cells in cell culture and tumour growth and metastasis in mouse models, MACC1 also contributes to carcinogenesis and progression of colorectal cancer through the β-catenin signalling pathway and mesenchymal-epithelial transition. MACC1 knockdown with si/sh RNA was investigated in cell lines of different types of cancer. MACC1 is a promising therapeutic target for antitumour and antimetastatic intervention strategies for cancers. Here, it is presented as a potential independent prognostic indicator of reduced overall survival as well as of the occurrence of distant metastasis in patients with different types of cancer.
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