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 in | The EMBO journal Vol. 31; no. 2; pp. 481 - 493 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
18.01.2012
Nature Publishing Group UK Blackwell Publishing Ltd Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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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. |
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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 |