Article
Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers.
American journal of respiratory and critical care medicine - 15 May 2006
Cantin André M, Hanrahan John W, Bilodeau Ginette, Ellis Lynda, Dupuis Annie, Liao Jie, Zielenski Julian, Durie Peter
Abstract excerpt
RATIONALE: Cigarette smoke extract inhibits chloride secretion in human bronchial epithelial cells. Oxidants decrease gene expression, protein expression, and function of the cystic fibrosis transmembrane conductance regulator (CFTR). OBJECTIVES: Because cigarette smoke is a rich source of oxidants, we verified the hypothesis that CFTR may be suppressed by exposure to cigarette smoke in vitro and in vivo....
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
