基因MDM2作为异常细胞增殖的生物标志物:综述

Gofur Nrp, Gofur Arp, Soesilaningtyas, Gofur Rnrp, M. Kahdina, Putri Hm
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引用次数: 0

摘要

癌症起源于正常细胞向异常细胞的增殖和分化。这个过程是正常细胞转变为癌细胞的过程。这个过程开始于正常细胞向癌细胞的起始、促进和进展过程。在正常情况下,细胞的分裂、增殖和分化受到很好的控制。非致死性基因缺陷是致癌性的核心。由于环境影响,如化学物质、辐射、病毒或生殖细胞遗传,可能发生遗传损伤或突变。这些基因通过调节细胞周期检查点来抑制生长,这些检查点被称为看门人,而基因稳定的守护者,保护基因组被称为看护人。正常情况下携带核糖体L5蛋白,携带p300 / CBP (CREAM结合蛋白)。最近,该结构域被发现有助于p53的降解,因为来自该结构域的突变MDM2能够降解p53。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gene MDM2 as Biomarker Proliferation of Abnormal Cells: A Review Article
Cancer begins due to the proliferation and differentiation of normal cells into abnormal cells. This process is a change in normal cells into cancer cells. This process begins with the process of initiation, promotion and progression from normal cells to cancer cells. Under normal conditions, cell division, proliferation and differentiation are well controlled. Non-lethal genetic defects are central to carcinogenesis. Genetic damage or mutation can occur due to environmental influences such as chemicals, radi -ation, viruses or inherited in germinativum cells. These genes inhibit growth by regulating cell cycle checkpoints, called gatekeep-ers, while guardians of gene stability, protecting the genome are called caretakers. Under normal circumstances with ribosomal L5 protein, and with p300 / CBP (CREAM Binding Protein). Recently, this domain was found to contribute to p53 degradation because the mutant MDM2 from this domain was able to degrade p53.
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