MYBPH, a transcriptional target of TTF-1, inhibits ROCK1, and reduces cell motility and metastasis

Cell migration driven by actomyosin filament assembly is a critical step in tumour invasion and metastasis. Herein, we report identification of myosin binding protein H ( MYBPH ) as a transcriptional target of TTF‐1 (also known as NKX2‐1 and TITF1 ), a master regulator of lung development that also...

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Published inThe EMBO journal Vol. 31; no. 2; pp. 481 - 493
Main Authors Hosono, Yasuyuki, Yamaguchi, Tomoya, Mizutani, Eri, Yanagisawa, Kiyoshi, Arima, Chinatsu, Tomida, Shuta, Shimada, Yukako, Hiraoka, Michiyo, Kato, Seiichi, Yokoi, Kohei, Suzuki, Motoshi, Takahashi, Takashi
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 18.01.2012
Nature Publishing Group UK
Blackwell Publishing Ltd
Nature Publishing Group
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Summary:Cell migration driven by actomyosin filament assembly is a critical step in tumour invasion and metastasis. Herein, we report identification of myosin binding protein H ( MYBPH ) as a transcriptional target of TTF‐1 (also known as NKX2‐1 and TITF1 ), a master regulator of lung development that also plays a role as a lineage‐survival oncogene in lung adenocarcinoma development. MYBPH inhibited assembly competence‐conferring phosphorylation of the myosin regulatory light chain (RLC) as well as activating phosphorylation of LIM domain kinase (LIMK), unexpectedly through its direct physical interaction with Rho kinase 1 (ROCK1) rather than with RLC. Consequently, MYBPH inhibited ROCK1 and negatively regulated actomyosin organization, which in turn reduced single cell motility and increased collective cell migration, resulting in decreased cancer invasion and metastasis. Finally, we also show that MYBPH is epigenetically inactivated by promoter DNA methylation in a fraction of TTF‐1 ‐positive lung adenocarcinomas, which appears to be in accordance with its deleterious functions in lung adenocarcinoma invasion and metastasis, as well as with the paradoxical association of TTF‐1 expression with favourable prognosis in lung adenocarcinoma patients. The TTF‐1 transcription factor is upregulated in lung adenocarcinomas, where it apparently suppresses malignant progression. One of its targets, MYBPH, inhibits Rho kinase 1 and hence cell motility and invasion, providing a potential explanation for the protective function of TTF‐1.
Bibliography:istex:7E031A4AFF8CEDF30B3C930182B863EE3895EF9C
ark:/67375/WNG-L3FD5WDW-N
ArticleID:EMBJ2011416
Supplementary InformationFigure source data filesReview Process File
ISSN:0261-4189
1460-2075
DOI:10.1038/emboj.2011.416