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The Rb tumor suppressor regulates epithelial cell migration and polarity.


ABSTRACT: Altered cell polarity and migration are hallmarks of cancer and metastases. Here we show that inactivation of the retinoblastoma gene (Rb) tumor suppressor causes defects in tissue closure that reflect the inability of Rb null epithelial cells to efficiently migrate and polarize. These defects occur independently of pRB's anti-proliferative role and instead correlate with upregulation of RhoA signaling and mislocalization of apical-basal polarity proteins. Notably, concomitant inactivation of tp53 specifically overrides the motility defect, and not the aberrant polarity, thereby uncovering previously unappreciated mechanisms by which Rb and tp53 mutations cooperate to promote cancer development and metastases.

SUBMITTER: Parisi T 

PROVIDER: S-EPMC6168347 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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The Rb tumor suppressor regulates epithelial cell migration and polarity.

Parisi Tiziana T   Balsamo Michele M   Gertler Frank F   Lees Jacqueline A JA  

Molecular carcinogenesis 20180826 11


Altered cell polarity and migration are hallmarks of cancer and metastases. Here we show that inactivation of the retinoblastoma gene (Rb) tumor suppressor causes defects in tissue closure that reflect the inability of Rb null epithelial cells to efficiently migrate and polarize. These defects occur independently of pRB's anti-proliferative role and instead correlate with upregulation of RhoA signaling and mislocalization of apical-basal polarity proteins. Notably, concomitant inactivation of tp  ...[more]

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