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Article: Cancer stemness in hepatocellular carcinoma: mechanisms and translational potential

TitleCancer stemness in hepatocellular carcinoma: mechanisms and translational potential
Authors
Keywordscancer genetics
cancer stem cell
carcinogenesis
cell component
cell differentiation
Issue Date2020
PublisherSpringer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc
Citation
British Journal of Cancer, 2020, v. 122 n. 10, p. 1428-1440 How to Cite?
AbstractCancer stemness, referring to the stem-cell-like phenotype of cancer cells, has been recognised to play important roles in different aspects of hepatocarcinogenesis. A number of well-established cell-surface markers already exist for liver cancer stem cells, with potential new markers of liver cancer stem cells being identified. Both genetic and epigenetic factors that affect various signalling pathways are known to contribute to cancer stemness. In addition, the tumour microenvironment—both physical and cellular—is known to play an important role in regulating cancer stemness, and the potential interaction between cancer stem cells and their microenvironment has provided insight into the regulation of the tumour-initiating ability as well as the cellular plasticity of liver CSCs. Potential specific therapeutic targeting of liver cancer stemness is also discussed. With increased knowledge, effective druggable targets might be identified, with the aim of improving treatment outcome by reducing chemoresistance.
Persistent Identifierhttp://hdl.handle.net/10722/286400
ISSN
2021 Impact Factor: 9.075
2020 SCImago Journal Rankings: 2.833
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTsui, YM-
dc.contributor.authorChan, LK-
dc.contributor.authorNg, IOL-
dc.date.accessioned2020-08-31T07:03:21Z-
dc.date.available2020-08-31T07:03:21Z-
dc.date.issued2020-
dc.identifier.citationBritish Journal of Cancer, 2020, v. 122 n. 10, p. 1428-1440-
dc.identifier.issn0007-0920-
dc.identifier.urihttp://hdl.handle.net/10722/286400-
dc.description.abstractCancer stemness, referring to the stem-cell-like phenotype of cancer cells, has been recognised to play important roles in different aspects of hepatocarcinogenesis. A number of well-established cell-surface markers already exist for liver cancer stem cells, with potential new markers of liver cancer stem cells being identified. Both genetic and epigenetic factors that affect various signalling pathways are known to contribute to cancer stemness. In addition, the tumour microenvironment—both physical and cellular—is known to play an important role in regulating cancer stemness, and the potential interaction between cancer stem cells and their microenvironment has provided insight into the regulation of the tumour-initiating ability as well as the cellular plasticity of liver CSCs. Potential specific therapeutic targeting of liver cancer stemness is also discussed. With increased knowledge, effective druggable targets might be identified, with the aim of improving treatment outcome by reducing chemoresistance.-
dc.languageeng-
dc.publisherSpringer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc-
dc.relation.ispartofBritish Journal of Cancer-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcancer genetics-
dc.subjectcancer stem cell-
dc.subjectcarcinogenesis-
dc.subjectcell component-
dc.subjectcell differentiation-
dc.titleCancer stemness in hepatocellular carcinoma: mechanisms and translational potential-
dc.typeArticle-
dc.identifier.emailTsui, YM: ymtsui@hku.hk-
dc.identifier.emailChan, LK: lkchan1@hku.hk-
dc.identifier.emailNg, IOL: iolng@hku.hk-
dc.identifier.authorityChan, LK=rp02289-
dc.identifier.authorityNg, IOL=rp00335-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41416-020-0823-9-
dc.identifier.pmid32231294-
dc.identifier.pmcidPMC7217836-
dc.identifier.scopuseid_2-s2.0-85082927906-
dc.identifier.hkuros313907-
dc.identifier.volume122-
dc.identifier.issue10-
dc.identifier.spage1428-
dc.identifier.epage1440-
dc.identifier.isiWOS:000522379800004-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0007-0920-

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