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Nitric oxide inactivates the retinoblastoma pathway in chronic inflammation.


ABSTRACT: Patients with chronic inflammatory bowel disease have a high risk of colon cancer. The molecules that initiate and promote colon cancer and the cancer pathways altered remain undefined. Here, using in vitro models and a mouse model of colitis, we show that nitric oxide (NO) species induce retinoblastoma protein (pRb) hyperphosphorylation and inactivation, resulting in increased proliferation through the pRb-E2F1 pathway. NO-driven pRb hyperphosphorylation occurs through soluble guanylyl cyclase/guanosine 3',5'-cyclic monophosphate signaling and is dependent on the mitogen-activated protein kinase/extracellular signal-regulated kinase kinase MEK/ERK and phosphatidylinositol 3-kinase/AKT pathways. Our results reveal a link between NO and pRb inactivation and provide insight into molecules that can be targeted in the prevention of the inflammation-to-cancer sequence.

SUBMITTER: Ying L 

PROVIDER: S-EPMC2752153 | biostudies-literature | 2007 Oct

REPOSITORIES: biostudies-literature

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Nitric oxide inactivates the retinoblastoma pathway in chronic inflammation.

Ying Lei L   Hofseth Anne B AB   Browning Darren D DD   Nagarkatti Mitzi M   Nagarkatti Prakash S PS   Hofseth Lorne J LJ  

Cancer research 20071001 19


Patients with chronic inflammatory bowel disease have a high risk of colon cancer. The molecules that initiate and promote colon cancer and the cancer pathways altered remain undefined. Here, using in vitro models and a mouse model of colitis, we show that nitric oxide (NO) species induce retinoblastoma protein (pRb) hyperphosphorylation and inactivation, resulting in increased proliferation through the pRb-E2F1 pathway. NO-driven pRb hyperphosphorylation occurs through soluble guanylyl cyclase/  ...[more]

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