Please use this identifier to cite or link to this item: https://doi.org/10.1093/gastro/goaa066
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dc.titleMetabolic alterations and vulnerabilities in hepatocellular carcinoma
dc.contributor.authorTenen, Daniel G.
dc.contributor.authorChai, Li
dc.contributor.authorTan, Justin L.
dc.date.accessioned2022-10-13T01:15:49Z
dc.date.available2022-10-13T01:15:49Z
dc.date.issued2020-11-18
dc.identifier.citationTenen, Daniel G., Chai, Li, Tan, Justin L. (2020-11-18). Metabolic alterations and vulnerabilities in hepatocellular carcinoma. Gastroenterology Report 9 (1) : 1-13. ScholarBank@NUS Repository. https://doi.org/10.1093/gastro/goaa066
dc.identifier.issn2052-0034
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/232866
dc.description.abstractLiver cancer is a serious disease. It is ranked as the cancer with the second highest number of cancer-related deaths worldwide. Hepatocellular carcinoma (HCC), which arises from transformed hepatocytes, is the major subtype of liver cancer. It accounts for 85% of total liver-cancer cases. An important aspect of HCC that has been actively studied is its metabolism. With the liver as the primary site of numerous metabolic processes in the body, it has been shown that the metabolism of HCC cells is highly dysregulated compared to that of normal hepatocytes. It is therefore crucial to understand the metabolic alterations caused by HCC and the underlying mechanisms for these alterations. This deeper understanding will allow diagnostic and therapeutic advancements in the treatment of HCC. In this review, we will summarize the current literature in HCC metabolic alterations, induced vulnerabilities, and potential therapeutic interventions. © 2020 The Author(s) 2020. Published by Oxford University Press and Sixth Affiliated Hospital of Sun Yat-sen University.
dc.publisherOxford University Press
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjecthepatocellular carcinoma (HCC)
dc.subjectmetabolic vulnerability
dc.subjectmetabolism
dc.subjecttargeted therapy
dc.typeReview
dc.contributor.departmentMEDICINE
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1093/gastro/goaa066
dc.description.sourcetitleGastroenterology Report
dc.description.volume9
dc.description.issue1
dc.description.page1-13
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