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Sex-Biased Molecular Signature for Overall Survival of Liver Cancer Patients

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dc.contributor.authorKim, Sun Young-
dc.contributor.authorSong, Hye Kyung-
dc.contributor.authorLee, Suk Kyeong-
dc.contributor.authorKim, Sang Geon-
dc.contributor.authorWoo, Hyun Goo-
dc.contributor.authorYang, Jieun-
dc.contributor.authorNoh, Hyun-Jin-
dc.contributor.authorKim, You-Sun-
dc.contributor.authorMoon, Aree-
dc.date.accessioned2023-04-27T20:41:00Z-
dc.date.available2023-04-27T20:41:00Z-
dc.date.issued2020-11-
dc.identifier.issn1976-9148-
dc.identifier.issn2005-4483-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/5958-
dc.description.abstractSex/gender disparity has been shown in the incidence and prognosis of many types of diseases, probably due to differences in genes, physiological conditions such as hormones, and lifestyle between the sexes. The mortality and survival rates of many cancers, especially liver cancer, differ between men and women. Due to the pronounced sex/gender disparity, considering sex/ gender may be necessary for the diagnosis and treatment of liver cancer. By analyzing research articles through a PubMed literature search, the present review identified 12 genes which showed practical relevance to cancer and sex disparities. Among the 12 sex-specific genes, 7 genes (BAP1, CTNNB1, FOXA1, GSTO1, GSTP1, IL6, and SRPK1) showed sex-biased function in liver cancer. Here we summarized previous findings of cancer molecular signature including our own analysis, and showed that sex-biased molecular signature CTNNB1(High), IL6(High), RHOA(High) and GLIPR1(Low) may serve as a female-specific index for prediction and evaluation of OS in liver cancer patients. This review suggests a potential implication of sex-biased molecular signature in liver cancer, providing a useful information on diagnosis and prediction of disease progression based on gender.-
dc.format.extent12-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC APPLIED PHARMACOLOGY-
dc.titleSex-Biased Molecular Signature for Overall Survival of Liver Cancer Patients-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.4062/biomolther.2020.157-
dc.identifier.scopusid2-s2.0-85094130150-
dc.identifier.wosid000614912400001-
dc.identifier.bibliographicCitationBIOMOLECULES & THERAPEUTICS, v.28, no.6, pp 491 - 502-
dc.citation.titleBIOMOLECULES & THERAPEUTICS-
dc.citation.volume28-
dc.citation.number6-
dc.citation.startPage491-
dc.citation.endPage502-
dc.type.docTypeReview-
dc.identifier.kciidART002638296-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusHEPATOCELLULAR-CARCINOMA PROGRESSION-
dc.subject.keywordPlusMALE-FEMALE DIFFERENCES-
dc.subject.keywordPlusESTROGEN RECEPTOR-BETA-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusX-CHROMOSOME-
dc.subject.keywordPlusWNT/BETA-CATENIN-
dc.subject.keywordPlusDNA METHYLATION-
dc.subject.keywordPlusSIGNALING PATHWAY-
dc.subject.keywordPlusGENDER DISPARITY-
dc.subject.keywordPlusCELL PHENOTYPE-
dc.subject.keywordAuthorLiver cancer-
dc.subject.keywordAuthorSex/gender-
dc.subject.keywordAuthorOverall survival-
dc.subject.keywordAuthorGene expression-
dc.subject.keywordAuthorMolecular signature-
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