Chen Bolin, Chakrobortty Nandita, Saha Apu Kumar, Shang Xuequn
School of Computer Science, Northwestern Polytechnical University, Xi'an, Shaanxi, China.
MIIT Key Laboratory of Big Data Storage and Management, Northwestern Polytechnical University, Xi'an, Shaanxi, China.
Front Genet. 2023 Jan 19;14:1120185. doi: 10.3389/fgene.2023.1120185. eCollection 2023.
In the world, colon cancer is regarded as one of the most common deadly cancer. Due to the lack of a better understanding of its prognosis system, this prevailing cancer has the second-highest morbidity and mortality rate compared with other cancers. A variety of genes are responsible to participate in colon cancer and the molecular mechanism is almost unsure. In addition, various studies have been done to identify the differentially expressed genes to investigate the dysfunctions of the genes but most of them did it individually. In this study, we constructed a functional interaction network for identifying the group of genes that conduct cellular functions and Protein-Protein Interaction network, which aims to better understanding protein functions and their biological relationships. A functional evolution network was also generated to analyze the dysfunctions from initial stage to later stage of colon cancer by investigating the gene modules and their molecular functions. The results show that the proposed evolution network is able to detect the significant cellular functions, which can be used to explore the evolution process of colon cancer. Moreover, a total of 10 core genes associated with colon cancer were identified, which were INS, SNAP25, GRIA2, SST, GCG, PVALB, SLC17A7, SLC32A1, SLC17A6, and NPY, respectively. The responsible candidate genes and corresponding pathways presented in this study could be used to develop new tumor indicators and novel therapeutic targets for the prevention and treatment of colon cancer.
在全球范围内,结肠癌被视为最常见的致命癌症之一。由于对其预后系统缺乏更深入的了解,这种常见癌症的发病率和死亡率在所有癌症中位居第二。多种基因参与结肠癌的发生,但其分子机制尚不清楚。此外,已有多项研究致力于识别差异表达基因以探究基因功能异常,但大多是单独进行的。在本研究中,我们构建了一个功能相互作用网络来识别执行细胞功能的基因群以及蛋白质 - 蛋白质相互作用网络,旨在更好地理解蛋白质功能及其生物学关系。还生成了一个功能进化网络,通过研究基因模块及其分子功能来分析结肠癌从早期到晚期的功能异常。结果表明,所提出的进化网络能够检测到重要的细胞功能,可用于探索结肠癌的进化过程。此外,共鉴定出10个与结肠癌相关的核心基因,分别为胰岛素(INS)、突触小体相关蛋白25(SNAP25)、谷氨酸受体离子型AMPA2(GRIA2)、生长抑素(SST)、胰高血糖素(GCG)、小白蛋白(PVALB)、溶质载体家族17成员7(SLC17A7)、溶质载体家族32成员1(SLC32A1)、溶质载体家族17成员6(SLC17A6)和神经肽Y(NPY)。本研究中提出的相关候选基因和相应途径可用于开发新的肿瘤指标以及预防和治疗结肠癌的新型治疗靶点。