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P53-induced microRNA-107 inhibits HIF-1 and tumor angiogenesis.


ABSTRACT: The pathway involving the tumor suppressor gene TP53 can regulate tumor angiogenesis by unclear mechanisms. Here we show that p53 regulates hypoxic signaling through the transcriptional regulation of microRNA-107 (miR-107). We found that miR-107 is a microRNA expressed by human colon cancer specimens and regulated by p53. miR-107 decreases hypoxia signaling by suppressing expression of hypoxia inducible factor-1beta (HIF-1beta). Knockdown of endogenous miR-107 enhances HIF-1beta expression and hypoxic signaling in human colon cancer cells. Conversely, overexpression of miR-107 inhibits HIF-1beta expression and hypoxic signaling. Furthermore, overexpression of miR-107 in tumor cells suppresses tumor angiogenesis, tumor growth, and tumor VEGF expression in mice. Finally, in human colon cancer specimens, expression of miR-107 is inversely associated with expression of HIF-1beta. Taken together these data suggest that miR-107 can mediate p53 regulation of hypoxic signaling and tumor angiogenesis.

SUBMITTER: Yamakuchi M 

PROVIDER: S-EPMC2851979 | biostudies-literature | 2010 Apr

REPOSITORIES: biostudies-literature

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P53-induced microRNA-107 inhibits HIF-1 and tumor angiogenesis.

Yamakuchi Munekazu M   Lotterman Craig D CD   Bao Clare C   Hruban Ralph H RH   Karim Baktiar B   Mendell Joshua T JT   Huso David D   Lowenstein Charles J CJ  

Proceedings of the National Academy of Sciences of the United States of America 20100322 14


The pathway involving the tumor suppressor gene TP53 can regulate tumor angiogenesis by unclear mechanisms. Here we show that p53 regulates hypoxic signaling through the transcriptional regulation of microRNA-107 (miR-107). We found that miR-107 is a microRNA expressed by human colon cancer specimens and regulated by p53. miR-107 decreases hypoxia signaling by suppressing expression of hypoxia inducible factor-1beta (HIF-1beta). Knockdown of endogenous miR-107 enhances HIF-1beta expression and h  ...[more]

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