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A signature predicting relapse based on integrated analysis on relapse-associated alternative mRNA splicing in I–III rectal cancer

机译:基于I-III直肠癌复发相关替代MRNA剪接综合分析的签名预测复发

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Researches focusing on the effects of alternative splicing (AS) on relapse of rectal cancer is little and signature based on the AS is blank. In this study, bioinformatic analysis was performed to identify and analyze the relapse-associated ASs, a signature was also constructed. In conclusion, 829 relapse-associated ASs of 676 mRNA were identified. 603 proteins with 2119 interactions were involved in the PPI (protein-protein interactions) network. 43 relapse-associated ASs and 64 SFs (splicing factors) with 160 interactions were indicated. Finally, we built a robust signature to predict the relapse of I–III rectal cancer with a high AUC (0.98) of ROC at 1?year. Based on the ASs involved in the signature, 4 molecular subgroups that could distinguish the relapse rate in diverse groups were identified. Our research provided an overview of relapse-associated ASs in I–III rectal cancer.
机译:重点研究替代剪接(AS)对直肠癌复发的影响几乎没有基于空白的签名。在这项研究中,进行生物信息分析以识别和分析复发相关的屁股,也构建了签名。总之,确定了829例复发相关的屁股676 mRNA。具有2119个相互作用的603蛋白涉及PPI(蛋白质 - 蛋白质相互作用)网络。 43复发相关ass和64个SFS(拼接因子)具有160个相互作用。最后,我们建立了一个稳健的签名,以预测1年的高AUC(0.98)Roc的I-III直肠癌的复发。基于签署签名的屁股,确定了4个可以区分各种组中复发率的分子亚组。我们的研究提供了在I-III直肠癌中复发相关屁股的概述。

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