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Vesicle-associated protein that interacts with G-alpha (GIV) as a predictive marker in stage II colorectal cancer

机译:与G-alpha(GIV)相互作用的囊泡相关蛋白作为II期结直肠癌的预测标志物

摘要

Method for analyzing a stage II colorectal cancer (CRM) competent for mismatch repair (pMMR) sample obtained from a subject, comprising: contacting a sample comprising stage II CRC pMMR with a specific binding agent a vesicle-associated protein protein that interacts with full-length G-alpha (GIV-fl), in which the protein-specific binding agent GIV-fl comprises an antibody against GIV-fl, or contacting isolated RNA from a sample with a nucleic acid probe specific for vesicle-associated protein mRNA that interacts with full-length G-alpha (GIV-fl); score the expression of mRNA or GIV-fl protein in the sample to determine a GIV-fl state of the sample; determining the lymphovascular invasion (LVI) status of the CRC in the subject with a specific binding agent that allows a determination of LVI in which the specific binding agent that allows a determination of LVI comprises a specific antibody for CD34 or lymphatic endothelium; and analyzing the sample based on the GIV-fl state and LVI state, in which the method further comprises determining the sample's mismatch repair status (MMR) with the binding agent specific for mating repair protein. erroneous, wherein the erroneous mating repair protein-specific binding agent comprises one or more antibodies specific for mutL 1 (MLH1) homolog; increased postmeiotic segregation 2 (PMS2); MutS 2 protein homolog Msh2 (MSH2) and / or MutS 6 protein homolog (MSH6); and in which the method is a method of predicting the probable progression-free survival (PFS) of the subject, in which more LVI and high GIV-fl levels are associated with a higher probability of recurrence.
机译:用于分析可从受试者获得的具有错配修复(pMMR)样品能力的II期结直肠癌(CRM)的方法,该方法包括:使包含II期CRC pMMR的样品与特异性结合剂接触与全脂相互作用的囊泡相关蛋白长度为G-alpha(GIV-fl),其中蛋白质特异性结合剂GIV-fl包含针对GIV-fl的抗体,或将样品中分离出的RNA与对与囊泡相关的蛋白质mRNA相互作用的核酸探针具有特异性全长G-alpha(GIV-fl);对样品中mRNA或GIV-f1蛋白的表达进行评分以确定样品的GIV-f1状态;用允许测定LVI的特异性结合剂确定受试者中CRC的淋巴管浸润(LVI)状态,其中允许测定LVI的特异性结合剂包含针对CD34或淋巴管内皮的特异性抗体;根据GIV-f1状态和LVI状态分析样品,其中该方法还包括用对交配修复蛋白特异的结合剂确定样品的错配修复状态(MMR)。错误的,其中错误的交配修复蛋白特异性结合剂包含一种或多种对mutL 1(MLH1)同源物具有特异性的抗体;减数分裂后隔离2(PMS2)增加; MutS 2蛋白同源物Msh2(MSH2)和/或MutS 6蛋白同源物(MSH6);并且其中所述方法是预测受试者的可能无进展生存(PFS)的方法,其中更多的LVI和高的GIV-f1水平与更高的复发概率相关。

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