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Pan-Cancer Analysis Reveals Distinct Metabolic Reprogramming in Different Epithelial-Mesenchymal Transition Activity States

DC Field Value Language
dc.contributor.author정재호-
dc.date.accessioned2022-01-26T01:58:25Z-
dc.date.available2022-01-26T01:58:25Z-
dc.date.issued2021-04-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/187418-
dc.description.abstractEpithelial-mesenchymal transition (EMT) is critical for cancer development, invasion, and metastasis. Its activity influences metabolic reprogramming, tumor aggressiveness, and patient survival. Abnormal tumor metabolism has been identified as a cancer hallmark and is considered a potential therapeutic target. We profiled distinct metabolic signatures by EMT activity using data from 9452 transcriptomes across 31 different cancer types from The Cancer Genome Atlas. Our results demonstrated that ~80 to 90% of cancer types had high carbohydrate and energy metabolism, which were associated with the high EMT group. Notably, among the distinct EMT activities, metabolic reprogramming in different immune microenvironments was correlated with patient prognosis. Nine cancer types showed a significant difference in survival with the presence of high EMT activity. Stomach cancer showed elevated energy metabolism and was associated with an unfavorable prognosis (p < 0.0068) coupled with high expression of CHST14, indicating that it may serve as a potential drug target. Our analyses highlight the prevalence of cancer type-dependent EMT and metabolic reprogramming activities and identified metabolism-associated genes that may serve as potential therapeutic targets.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherMDPI-
dc.relation.isPartOfCANCERS-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titlePan-Cancer Analysis Reveals Distinct Metabolic Reprogramming in Different Epithelial-Mesenchymal Transition Activity States-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Surgery (외과학교실)-
dc.contributor.googleauthorJi-Yong Sung-
dc.contributor.googleauthorJae-Ho Cheong-
dc.identifier.doi10.3390/cancers13081778-
dc.contributor.localIdA03717-
dc.relation.journalcodeJ03449-
dc.identifier.eissn2072-6694-
dc.identifier.pmid33917859-
dc.subject.keywordenergy metabolism-
dc.subject.keywordepithelial–mesenchymal transition-
dc.subject.keywordmetabolic reprogramming-
dc.subject.keywordsurvival-
dc.subject.keywordtumor immune microenvironment-
dc.contributor.alternativeNameCheong, Jae Ho-
dc.contributor.affiliatedAuthor정재호-
dc.citation.volume13-
dc.citation.number8-
dc.citation.startPage1778-
dc.identifier.bibliographicCitationCANCERS, Vol.13(8) : 1778, 2021-04-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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