2022
DOI: 10.1109/tcbb.2021.3106344
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Identifying Cancer Patient Subgroups by Finding Co-Modules From the Driver Mutation Profiles and Downstream Gene Expression Profiles

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Cited by 9 publications
(3 citation statements)
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“…Most somatic mutations of the EGFR gene associated with lung adenocarcinoma cause abnormal expression of the KRAS gene, which can continuously activate the EGFR signaling pathway and eventually enhance cell proliferation, leading to the generation of cancer. The ATM gene provides instructions for Entropy 2023, 25, 841 10 of 16 making proteins, mainly in the nucleus, where it helps control the rate at which cells grow and divide [37][38][39]. This protein also plays an important role in the normal development and activities of several body systems, including the nervous system and the immune system.…”
Section: K (Number Of Genes In Pathway)mentioning
confidence: 99%
“…Most somatic mutations of the EGFR gene associated with lung adenocarcinoma cause abnormal expression of the KRAS gene, which can continuously activate the EGFR signaling pathway and eventually enhance cell proliferation, leading to the generation of cancer. The ATM gene provides instructions for Entropy 2023, 25, 841 10 of 16 making proteins, mainly in the nucleus, where it helps control the rate at which cells grow and divide [37][38][39]. This protein also plays an important role in the normal development and activities of several body systems, including the nervous system and the immune system.…”
Section: K (Number Of Genes In Pathway)mentioning
confidence: 99%
“…These techniques identify SMG with genetic variation that are considerably greater than that of the background mutation rate and classify those as driving genes. The majority of cancer driver gene research has been on identifying single somatic point mutations [12]. Somatic mutations, on the other hand, are typically very diverse within cancer genomes, within the same kind of cancer, and account for only a tiny part of genomic changes [3] [19] [20] [21].…”
Section: Introductionmentioning
confidence: 99%
“…Other genomic elements, including as nonsense mutations, penetrations, and omissions, as well as germ line variations, have been previously overlooked but now have recently been discovered to play an important effect on cancer formation [9] [21] [22]. When genomic components, such as somatic mutations, germ line variations, insertions and deletions, are investigated jointly, particularly inside an interaction term, modeling intricacy as well as investigation strength are obstacles [12]. To evaluate the influence of genetic mutations on modifications in gene expression patterns, Tang et al [10] used a semi-local centrality measure and a gene mutation effect function in 2021.…”
Section: Introductionmentioning
confidence: 99%