4.6 Article

S-Nitrosoglutathione Reductase in Human Lung Cancer

Journal

Publisher

AMER THORACIC SOC
DOI: 10.1165/rcmb.2011-0147OC

Keywords

lung cancer; S-nitrosoglutathione reductase; Ras

Funding

  1. National Institutes of Health/National Heart, Lung, and Blood Institute [3R01HL59337, P01HL101871-01A1, 2R01HL69170]

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S-Nitrosoglutathione (GSNO) reductase regulates cell signaling pathways relevant to asthma and protects cells from nitrosative stress. Recent evidence suggests that this enzyme may prevent human hepatocellular carcinoma arising in the setting of chronic hepatitis. We hypothesized that GSNO reductase may also protect the lung against potentially carcinogenic reactions associated with nitrosative stress. We report that wild-type Ras is S-nitrosylated and activated by nitrosative stress and that it is denitrosylated by GSNO reductase. In human lung cancer, the activity and expression of GSNO reductase are decreased. Further, the distribution of the enzyme(including its colocalization with wild-type Ras) is abnormal. We conclude that decreased activity of GSNO reductase could leave the human lung vulnerable to the oncogenic effects of nitrosative stress, as is the case in the liver. This potential should be considered when developing therapies that inhibit pulmonary GSNO reductase to treat asthma and other conditions.

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