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FBXW7-mediated stability regulation of signal transducer and activator of transcription 2 in melanoma formation.


ABSTRACT: In this study, we provide critical evidence that STAT2 stability regulation plays an essential role in melanoma cell proliferation and colony growth. We found that the interaction of FBXW7 and STAT2 induced STAT2 destabilization via a ubiquitination-mediated proteasomal degradation pathway. Notably, GSK3?-mediated STAT2 phosphorylation facilitated STAT2-FBXW7 interactions via the DNA binding domain of STAT2 and domains 1, 2, 6, and 7 of FBXW7 WD40. Importantly, the inverse correlation between protein levels of STAT2 and FBXW7 were observed not only in human melanoma cells but also in a human skin cancer tissue array. The relationship between protein levels of STAT2 and FBXW7, cell proliferation, and colony growth were similarly observed in the melanoma cell lines SK-MEL-2, -5, and -28. Moreover, STAT2 knockdown in melanoma cells suppressed melanoma cell proliferation and colony formation. These data demonstrated that FBXW7-mediated STAT2 stability regulation plays an essential role in melanoma cell proliferation and cancer growth.

SUBMITTER: Lee CJ 

PROVIDER: S-EPMC6955312 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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FBXW7-mediated stability regulation of signal transducer and activator of transcription 2 in melanoma formation.

Lee Cheol-Jung CJ   An Hyun-Jung HJ   Kim Seung-Min SM   Yoo Sun-Mi SM   Park Juhee J   Lee Ga-Eun GE   Kim Woo-Young WY   Kim Dae Joon DJ   Kang Han Chang HC   Lee Joo Young JY   Lee Hye Suk HS   Cho Sung-Jun SJ   Cho Yong-Yeon YY  

Proceedings of the National Academy of Sciences of the United States of America 20191216 1


In this study, we provide critical evidence that STAT2 stability regulation plays an essential role in melanoma cell proliferation and colony growth. We found that the interaction of FBXW7 and STAT2 induced STAT2 destabilization via a ubiquitination-mediated proteasomal degradation pathway. Notably, GSK3β-mediated STAT2 phosphorylation facilitated STAT2-FBXW7 interactions via the DNA binding domain of STAT2 and domains 1, 2, 6, and 7 of FBXW7 WD40. Importantly, the inverse correlation between pr  ...[more]

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