Survival analysis for the identified cancer gene subtype from the co-clustering algorithm

Logenthiran Machap, Kohbalan Moorthy
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Abstract

Cancer gene subtype information is significant for understanding tumour heterogeneity. The early detection of cancer and subsequent treatment can be lifesaving. However, it is hard clinically and computationally to detect cancer and its subtypes in their early stages. Therefore, we extend the analysis and results from Machap et al. (2019), to include the Kaplan-Meier survival analysis with the integration of gene expression and clinical features data. There are two cancer datasets used for the analysis: breast cancer and glioblastoma multiforme. The luminal type was the common subtype of breast cancer, showing a higher survival rate. Whereas the Proneural subtype in glioblastoma multiforme has a little longer survival rate than the other three subtypes. These molecular differences between subtypes have been shown to correlate very well with clinical features and survival parameters to help understand the disease and develop better therapeutic targets.
通过共聚类算法对鉴定出的癌症基因亚型进行生存分析
肿瘤基因亚型信息对了解肿瘤异质性具有重要意义。癌症的早期发现和随后的治疗可以挽救生命。然而,在临床和计算上很难在早期发现癌症及其亚型。因此,我们扩展了Machap等人(2019)的分析和结果,纳入了整合基因表达和临床特征数据的Kaplan-Meier生存分析。有两种癌症数据集用于分析:乳腺癌和多形性胶质母细胞瘤。腔型是乳腺癌的常见亚型,生存率较高。而多形性胶质母细胞瘤的前膜亚型比其他三种亚型生存率稍长。这些亚型之间的分子差异已被证明与临床特征和生存参数非常相关,有助于了解疾病并开发更好的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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