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Lung and lymph node metastases from hepatocellular carcinoma: Comparison of pathological aspects

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dc.contributor.author김도영-
dc.contributor.author김세훈-
dc.contributor.author박영년-
dc.contributor.author우하영-
dc.contributor.author유정은-
dc.contributor.author이형진-
dc.contributor.author이혜선-
dc.contributor.author최기홍-
dc.date.accessioned2022-03-11T05:54:32Z-
dc.date.available2022-03-11T05:54:32Z-
dc.date.issued2022-01-
dc.identifier.issn1478-3223-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/187859-
dc.description.abstractBackground & aims: Extrahepatic metastasis from hepatocellular carcinoma (HCC) is a catastrophic event, yet organ-specific pathological characteristics of metastatic HCC remain unclear. We aimed to characterize the pathological aspects of HCC metastases to various organs. Methods: We collected intrahepatic HCC (cohort 1, n = 322) and extrahepatic metastatic HCC (cohort 2, n = 130) samples. Clinicopathological evaluation and immunostaining for K19, CD34, αSMA, fibroblast-associated protein (FAP), CAIX, VEGF, PD-L1, CD3, CD8, Foxp3, CD163 and epithelial-mesenchymal transition (EMT)-related markers were performed. Results: Independent factors for extrahepatic metastasis included BCLC stage B-C, microvascular invasion (MVI), vessels encapsulating tumour clusters (VETC)-HCC, K19 and FAP expression, and CD163+ macrophage infiltration (cohort 1, P < .05 for all). Lung metastases (n = 63) had the highest proportion of VETC-HCC and macrotrabecular-massive (MTM)-HCC. Lymph node metastases (n = 19) showed significantly high rates of EMT-high features, K19 expression, fibrous tumour stroma with αSMA and FAP expression, high immune cell infiltration, PD-L1 expression (combined positive score), CD3+, CD8+, Foxp3+ T cell and CD163+ macrophage infiltration (adjusted P < .05 for all). In both cohorts, EMT-high HCCs showed higher rates of K19 expression, fibrous tumour stroma, high immune cell infiltration, PD-L1 expression and CD3+ T cell infiltration, whereas EMT-low HCCs were more frequent among VETC-HCCs (P < .05 for all). Overall phenotypic features were not significantly different between paired primary-metastatic HCCs (n = 32). Conclusions: Metastatic HCCs to various organs showed different pathological features. VETC and MTM subtypes were related to lung metastasis, whereas K19 expression, EMT-high features with fibrous tumour stroma and high immune cell infiltration were related to lymph node metastasis.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherWiley-Blackwell-
dc.relation.isPartOfLIVER INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHCarcinoma, Hepatocellular* / pathology-
dc.subject.MESHEpithelial-Mesenchymal Transition-
dc.subject.MESHHumans-
dc.subject.MESHLiver Neoplasms* / pathology-
dc.subject.MESHLung-
dc.subject.MESHLymphatic Metastasis-
dc.titleLung and lymph node metastases from hepatocellular carcinoma: Comparison of pathological aspects-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorHa Young Woo-
dc.contributor.googleauthorHyungjin Rhee-
dc.contributor.googleauthorJeong Eun Yoo-
dc.contributor.googleauthorSe Hoon Kim-
dc.contributor.googleauthorGi Hong Choi-
dc.contributor.googleauthorDo Young Kim-
dc.contributor.googleauthorHyun Goo Woo-
dc.contributor.googleauthorHye Sun Lee-
dc.contributor.googleauthorYoung Nyun Park-
dc.identifier.doi10.1111/liv.15051-
dc.contributor.localIdA00385-
dc.contributor.localIdA00610-
dc.contributor.localIdA01563-
dc.contributor.localIdA04854-
dc.contributor.localIdA02504-
dc.contributor.localIdA05171-
dc.contributor.localIdA03312-
dc.contributor.localIdA04046-
dc.relation.journalcodeJ02171-
dc.identifier.eissn1478-3231-
dc.identifier.pmid34490997-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1111/liv.15051-
dc.subject.keywordepithelial-mesenchymal transition-
dc.subject.keywordextrahepatic metastasis-
dc.subject.keywordhepatocellular carcinoma-
dc.subject.keywordkeratin 19-
dc.subject.keywordmacrotrabecular-massive-
dc.subject.keywordvessels encapsulating tumour clusters-
dc.contributor.alternativeNameKim, Do Young-
dc.contributor.affiliatedAuthor김도영-
dc.contributor.affiliatedAuthor김세훈-
dc.contributor.affiliatedAuthor박영년-
dc.contributor.affiliatedAuthor우하영-
dc.contributor.affiliatedAuthor유정은-
dc.contributor.affiliatedAuthor이형진-
dc.contributor.affiliatedAuthor이혜선-
dc.contributor.affiliatedAuthor최기홍-
dc.citation.volume42-
dc.citation.number1-
dc.citation.startPage199-
dc.citation.endPage209-
dc.identifier.bibliographicCitationLIVER INTERNATIONAL, Vol.42(1) : 199-209, 2022-01-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Radiology (영상의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers

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