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MCM2 and MCM5 as Prognostic Markers in Colon Cancer: A Worthwhile Approach

机译:MCM2和MCM5作为结肠癌预后的标志物:一种值得的方法

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摘要

In their current report, Theocharis and coworkers analyze the relation of MCM2 and MCM5 with clinicopathology parameters and molecular parameters of cell proliferation and differentiation well established in colon cancer . While they found MCM2 to be consistently associated with clini-copathological parameters, Ki67 and p53, MCM5 was not. What makes this study so appealing? Besides its concise and straight-forward character, it deals with an interesting molecular parameter, minichromosome maintenance proteins (Mem). The Mem family members (Mcm2-7) are highly conserved replication initiation factors. Mem proteins are presumed to regulate replication by cyclical DNA-unwinding. They are integrated into pre-replicative complexes forming during the Gl phase of the cell cycle. Thereby they "license" chromatin for replication in the subsequent S phase. While Mem proteins are present in all phases of the proliferative cell cycle, they are absent in quiescent cells and in cellular senescence. The strict relation to chromatin replication renders the Mem protein family a novel class of proliferation marker . They are currently viewed as highly specific for proliferation . In contrast to Ki67, which was also analyzed in the current contribution by Theocharis, Mcm2 is an essential factor for initiation of DNA replication in eukaryotic cells. Thus Mem proteins have been suggested as excellent markers for tumor evaluation
机译:Theocharis及其同事在其最新报告中分析了MCM2和MCM5与结肠癌临床病理参数以及细胞增殖和分化的分子参数之间的关系。尽管他们发现MCM2与临床病理参数,Ki67和p53始终相关,但MCM5并非如此。是什么使这项研究如此吸引人?除了简洁明了的特点外,它还涉及一个有趣的分子参数,即微染色体维持蛋白(Mem)。 Mem家族成员(Mcm2-7)是高度保守的复制起始因子。推测Mem蛋白可通过循环DNA展开调节复制。它们被整合到在细胞周期的G1阶段形成的复制前复合物中。因此,他们“许可”染色质在随后的S期复制。尽管Mem蛋白存在于增生细胞周期的所有阶段,但它们在静止细胞和细胞衰老中不存在。与染色质复制的严格关系使Mem蛋白家族成为一类新的增殖标志。目前,它们被认为对增殖具有高度特异性。与Theocharis在目前的贡献中也进行过分析的Ki67相反,Mcm2是启动真核细胞中DNA复制的重要因素。因此,Mem蛋白被认为是评估肿瘤的极好的标志物

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