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Replication protein A is an independent prognostic indicator with potential therapeutic implications in colon cancer

机译:复制蛋白A是独立的预后指标,对结肠癌具有潜在的治疗意义

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Replication protein A (RPA), a component of the origin recognition complex, is required for stabilization of single-stranded DNA at early and later stages of DNA replication being thus critical for eukaryotic DNA replication. Experimental studies in colon cancer cell lines have shown that RPA protein may be the target of cytotoxins designed to inhibit cellular proliferation. This is the first study to investigate the expression of RPA1 and RPA2 subunits of RPA protein and assess their prognostic value in colon cancer patients. We analyzed immunohistochemically the expression of RPA1 and RPA2 proteins in a series of 130 colon cancer resection specimens in relation to conventional clinicopathological parameters and patients' survival. Statistical significant positive associations emerged between: (a) RPA1 and RPA2 protein expressions (P=0.0001), (b) RPA1 and RPA2 labelling indices (LIs) and advanced stage of the disease (P=0.001 and 0.003, respectively), (c) RPA1 and RPA2 LIs and the presence of lymph node metastasis (P=0.002 and 0.004, respectively), (d) RPA1 LI and the number of infiltrated lymph nodes (P=0.021), (e) RPA2 LI and histological grade of carcinomas (P=0.05). Moreover, a statistical significant higher RPA1 LI was observed in the metastatic sites compared to the original ones (P=0.012). RPA1 and RPA2 protein expression associated with adverse patients' outcome in both univariate (log rank test: PP=0.092 and 0.0001, respectively) statistical analysis. Statistical significant differences according to the expression of RPA1 and RPA2 proteins were also noticed in the survival of stage II (PP=0.0029 and 0.0079, respectively) patients. In conclusion, RPA1 and RPA2 proteins appear to be useful prognostic indicators in colon cancer patients and attractive therapeutic targets for regulation by tumor suppressors or other proteins involved in the control of cell proliferation.
机译:复制蛋白A(RPA)是起源识别复合物的一个组成部分,对于在DNA复制的早期和后期稳定单链DNA来说是必需的,因此对于真核DNA复制至关重要。在结肠癌细胞系中进行的实验研究表明,RPA蛋白可能是旨在抑制细胞增殖的细胞毒素的靶标。这是第一项研究RPA蛋白RPA1和RPA2亚基表达并评估其在结肠癌患者中的预后价值的研究。我们分析了130例结肠癌切除标本中与常规临床病理参数和患者生存相关的RPA1和RPA2蛋白的免疫组织化学表达。 (a)RPA1和RPA2蛋白表达(P = 0.0001),(b)RPA1和RPA2标记指数(LIs)与疾病晚期(分别为P = 0.001和0.003)之间存在统计学显着的正相关性(c )RPA1和RPA2 LIs和是否存在淋巴结转移(分别为P = 0.002和0.004),(d)RPA1 LI和浸润的淋巴结数目(P = 0.021),(e)RPA2 LI和癌的组织学等级(P = 0.05)。而且,与原始部位相比,在转移部位观察到统计学上显着更高的RPA1 LI(P = 0.012)。在单因素统计分析中,RPA1和RPA2蛋白表达均与不良患者的预后相关(对数秩检验:PP = 0.092和0.0001)。在II期患者(分别为PP = 0.0029和0.0079)的存活期中,还注意到了根据RPA1和RPA2蛋白表达的统计学显着差异。总之,RPA1和RPA2蛋白在结肠癌患者中似乎是有用的预后指标,并且是由肿瘤抑制因子或其他参与细胞增殖控制的蛋白调节的有吸引力的治疗靶标。

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