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dc.contributor.author Lee, Youngmin ko
dc.contributor.author Kim, Seokhyun ko
dc.contributor.author Kim, Minseok S. ko
dc.contributor.author Kim, Daecheol ko
dc.contributor.author Lee, Eunhee ko
dc.contributor.author Lee, Jusuk ko
dc.contributor.author Lee, Sunghun ko
dc.contributor.author Kim, Youngzoon ko
dc.date.accessioned 2021-01-22T07:03:54Z -
dc.date.available 2021-01-22T07:03:54Z -
dc.date.created 2020-12-17 -
dc.date.issued 2020-12 -
dc.identifier.citation Cancers, v.12, no.12, pp.3632 -
dc.identifier.issn 2072-6694 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/12661 -
dc.description.abstract Purpose: The objective of this study was to investigate the epigenetic role of histone lysine methylation/demethylation on the expression of epithelial-to-mesenchymal transition (EMT) associated transcriptional factors (TFs) during the metastasis of lung adenocarcinoma to the brain. Methods: Paired samples of lung adenocarcinoma and brain metastasis (BM) were analyzed in 46 individual patients. Both samples were obtained by surgical resection or biopsy of the lung and brain. The paraffin-fixed formalin-embedded samples were obtained from the pathology archives in our institute. In samples of lung adenocarcinoma and BM, immunohistochemical staining was performed for epithelial markers, mesenchymal markers, EMT-TFs, histone lysine methyltransferase and demethylase. Results: The immunoreactivity of EMT-TFs such as Slug (15.6% vs. 42.6%, p = 0.005), Twist (23.6% vs. 45.9%, p = 0.010) and ZEB1 (15.0% vs. 55.9%, p = 0.002) was increased in BM compared with that in lung adenocarcinoma. Epigenetic inducers such as H3K4 methyltransferase (MLL4, p = 0.018) and H3K36me3 demethylase (UTX, p = 0.003) were statistically increased, and epigenetic repressors such as EZH2 (H3K27 methyltransferase, p = 0.046) were significantly decreased in BM compared with those in lung adenocarcinoma. The expression of UTX-ZEB1 (R2 linear = 1.204) and MLL4-Slug (R2 linear = 0.987) was increased in direct proportion, and EZH2-Twist (R2 linear = −2.723) decreased in reverse proportion. Conclusions: The results suggest that certain histone lysine methyltransferase/demethylase, such as MLL4, UTX, and EZH2, regulate the expression of EMT-TFs such as Slug, ZEB1, and Twist epigenetically, which may thereby influence cancer metastasis from the lung to the brain. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. -
dc.language English -
dc.publisher MDPI AG -
dc.title Epigenetic Role of Histone Lysine Methyltransferase and Demethylase on the Expression of Transcription Factors Associated with the Epithelial-to-Mesenchymal Transition of Lung Adenocarcinoma Metastasis to the Brain -
dc.type Article -
dc.identifier.doi 10.3390/cancers12123632 -
dc.identifier.wosid 000601719000001 -
dc.identifier.scopusid 2-s2.0-85097246765 -
dc.type.local Article(Overseas) -
dc.type.rims ART -
dc.description.journalClass 1 -
dc.contributor.nonIdAuthor Lee, Youngmin -
dc.contributor.nonIdAuthor Kim, Seokhyun -
dc.contributor.nonIdAuthor Kim, Daecheol -
dc.contributor.nonIdAuthor Lee, Eunhee -
dc.contributor.nonIdAuthor Lee, Jusuk -
dc.contributor.nonIdAuthor Lee, Sunghun -
dc.contributor.nonIdAuthor Kim, Youngzoon -
dc.identifier.citationVolume 12 -
dc.identifier.citationNumber 12 -
dc.identifier.citationStartPage 3632 -
dc.identifier.citationTitle Cancers -
dc.type.journalArticle Article -
dc.description.isOpenAccess Y -
dc.subject.keywordAuthor lung cancer -
dc.subject.keywordAuthor brain metastasis -
dc.subject.keywordAuthor epigenome -
dc.subject.keywordAuthor histone modification -
dc.subject.keywordAuthor epithelial-to-mesenchymal transition -
dc.subject.keywordPlus POLYCOMB GROUP PROTEIN -
dc.subject.keywordPlus E-CADHERIN REPRESSION -
dc.subject.keywordPlus CELL CARCINOMA -
dc.subject.keywordPlus BREAST-CANCER -
dc.subject.keywordPlus STEM-CELLS -
dc.subject.keywordPlus EZH2 -
dc.subject.keywordPlus PROGRESSION -
dc.subject.keywordPlus REGULATOR -
dc.subject.keywordPlus PROGRAMS -
dc.subject.keywordPlus SURVIVAL -
dc.contributor.affiliatedAuthor Kim, Minseok S. -
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Department of New Biology BioDr. Lab - Nanobiomedicine 1. Journal Articles

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