The ETV6-NTRK3 chimeric tyrosine kinase suppresses TGF-β signaling by inactivating the TGF-β type II receptor = ETV6-NTRK3 chimeric 타이로신 카이네이스의 TGF-β 2형 수용체 불활성화에 의한 TGF-β 2

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dc.contributor.authorW Jin-
dc.contributor.authorB C Kim-
dc.contributor.authorC Tognon-
dc.contributor.authorHo Jae Lee-
dc.contributor.authorS Patel-
dc.contributor.authorC L Lannon-
dc.contributor.authorJ M Maris-
dc.contributor.authorT J Triche-
dc.contributor.authorP H B Sorensen-
dc.contributor.authorS J Kim-
dc.date.accessioned2017-04-19T09:03:37Z-
dc.date.available2017-04-19T09:03:37Z-
dc.date.issued2005-
dc.identifier.issn0027-8424-
dc.identifier.uri10.1073/pnas.0503137102ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7166-
dc.description.abstractAn emerging theme in cancer biology is that although some malignancies occur through the sequential acquisition of different genetic alterations, certain dominantly acting oncoproteins such as those associated with chromosomal translocations have multiple functions and do not require additional mutations for cell transformation. The ETV6-NTRK3 (EN) chimeric tyrosine kinase, a potent oncoprotein expressed in tumors derived from multiple cell lineages, functions as a constitutively active protein tyrosine kinase. Here, we show that EN suppresses TGF-β signaling by directly binding to the type II TGF-β receptor, thereby preventing it from interacting with the type I TGF-β receptor. This activity requires a functional EN protein tyrosine kinase, and type II TGF-β receptor appears to be a direct target of EN. Our findings provide evidence for a previously undescribed mechanism by which oncogenic tyrosine kinases can block TGF-β tumor suppressor activity.-
dc.publisherNatl Acad Sciences-
dc.titleThe ETV6-NTRK3 chimeric tyrosine kinase suppresses TGF-β signaling by inactivating the TGF-β type II receptor = ETV6-NTRK3 chimeric 타이로신 카이네이스의 TGF-β 2형 수용체 불활성화에 의한 TGF-β 2-
dc.title.alternativeThe ETV6-NTRK3 chimeric tyrosine kinase suppresses TGF-β signaling by inactivating the TGF-β type II receptor-
dc.typeArticle-
dc.citation.titleProceedings of National Academy of Sciences of United States of America-
dc.citation.number45-
dc.citation.endPage16244-
dc.citation.startPage16239-
dc.citation.volume102-
dc.contributor.affiliatedAuthorHo Jae Lee-
dc.contributor.alternativeName진욱-
dc.contributor.alternativeName김병철-
dc.contributor.alternativeNameTognon-
dc.contributor.alternativeName이호재-
dc.contributor.alternativeNamePatel-
dc.contributor.alternativeNameLannon-
dc.contributor.alternativeNameMaris-
dc.contributor.alternativeNameTriche-
dc.contributor.alternativeNameSorensen-
dc.contributor.alternativeName김성진-
dc.identifier.bibliographicCitationProceedings of National Academy of Sciences of United States of America, vol. 102, no. 45, pp. 16239-16244-
dc.identifier.doi10.1073/pnas.0503137102-
dc.subject.keywordchromosomal translocation-
dc.subject.keywordcongenital fibrosarcoma-
dc.subject.keywordTGF-β receptor-
dc.subject.localchromosomal translocation-
dc.subject.localcongenital fibrosarcoma-
dc.subject.localTGF-β receptor-
dc.description.journalClassY-
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