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HDAC2 promotes loss of primary cilia in pancreatic ductal adenocarcinoma.


ABSTRACT: Loss of primary cilia is frequently observed in tumor cells, including pancreatic ductal adenocarcinoma (PDAC) cells, suggesting that the absence of this organelle may promote tumorigenesis through aberrant signal transduction and the inability to exit the cell cycle. However, the molecular mechanisms that explain how PDAC cells lose primary cilia are still ambiguous. In this study, we found that inhibition or silencing of histone deacetylase 2 (HDAC2) restores primary cilia formation in PDAC cells. Inactivation of HDAC2 results in decreased Aurora A expression, which promotes disassembly of primary cilia. We further showed that HDAC2 controls ciliogenesis independently of Kras, which facilitates Aurora A expression. These studies suggest that HDAC2 is a novel regulator of primary cilium formation in PDAC cells.

SUBMITTER: Kobayashi T 

PROVIDER: S-EPMC5286357 | biostudies-literature | 2017 Feb

REPOSITORIES: biostudies-literature

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HDAC2 promotes loss of primary cilia in pancreatic ductal adenocarcinoma.

Kobayashi Tetsuo T   Nakazono Kosuke K   Tokuda Mio M   Mashima Yu Y   Dynlacht Brian David BD   Itoh Hiroshi H  

EMBO reports 20161227 2


Loss of primary cilia is frequently observed in tumor cells, including pancreatic ductal adenocarcinoma (PDAC) cells, suggesting that the absence of this organelle may promote tumorigenesis through aberrant signal transduction and the inability to exit the cell cycle. However, the molecular mechanisms that explain how PDAC cells lose primary cilia are still ambiguous. In this study, we found that inhibition or silencing of histone deacetylase 2 (HDAC2) restores primary cilia formation in PDAC ce  ...[more]

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