Shobha A. Akerkar
National Institutes of Health
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Featured researches published by Shobha A. Akerkar.
The New England Journal of Medicine | 1993
Stephen S. Hecht; Steven G. Carmella; Sharon E. Murphy; Shobha A. Akerkar; Klaus D. Brunnemann; Dietrich Hoffmann
BACKGROUND Environmental tobacco smoke has been classified by the Environmental Protection Agency as a carcinogen causally associated with lung cancer in adults, but there have been no reports of lung carcinogens or their metabolites in the body fluids or tissues of nonsmokers exposed to environmental tobacco smoke. METHODS Five male nonsmokers were exposed to sidestream cigarette smoke generated by machine smoking of reference cigarettes for 180 minutes on each of two days, six months apart. Sidestream smoke is the smoke that originates from the smoldering end of a cigarette between puffs. Twenty-four-hour urine samples were collected before and after exposure. The urine samples were analyzed for 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and its glucuronide, which are metabolites of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), a powerful lung carcinogen in rodents. NNAL is also a lung carcinogen in rodents. RESULTS The urinary excretion of the metabolites increased after exposure to sidestream smoke in all the men. The mean (+/- SD) amount of NNAL and NNAL glucuronide was significantly higher after exposure than at base line (33.9 +/- 20.0 vs. 8.4 +/- 11.2 ng per 24 hours [127 +/- 74 vs. 31 +/- 41 pmol per day], P < 0.001) and was correlated with urinary cotinine excretion (r = 0.89, P < 0.001). The nicotine concentrations in the air to which the men were exposed were comparable to those in a heavily smoke-polluted bar. CONCLUSIONS Nonsmokers exposed to sidestream cigarette smoke take up and metabolize a lung carcinogen, which provides experimental support for the proposal that environmental tobacco smoke can cause lung cancer.
Cancer Epidemiology, Biomarkers & Prevention | 2005
Bogdan Prokopczyk; Gerhard Leder; Neil Trushin; A. John Cunningham; Shobha A. Akerkar; Brian Pittman; Marco Ramadani; Joern Straeter; Hans G. Beger; Doris Henne-Bruns; Karam El-Bayoumy
Tobacco smoking is the only known etiologic agent that causes pancreatic cancer. The tobacco-specific nitrosamine 4-(methylnitrosamino)-I-(3-pyridyl)-1-butanone (NNK) is a potent carcinogen in laboratory rodents that, independent of the route of administration, induces primarily lung adenocarcinoma
Cancer Epidemiology, Biomarkers & Prevention | 1995
Stephen S. Hecht; Fung Lung Chung; John P. Richie; Shobha A. Akerkar; Anna Borukhova; Lisa Skowronski; Steven G. Carmella
Cancer Epidemiology, Biomarkers & Prevention | 1995
Steven G. Carmella; Shobha A. Akerkar; John P. Richie; Stephen S. Hecht
Cancer Research | 1993
Steven G. Carmella; Shobha A. Akerkar; Stephen S. Hecht
Cancer Epidemiology, Biomarkers & Prevention | 1997
John P. Richie; Steven G. Carmella; Joshua E. Muscat; Daniella G. Scott; Shobha A. Akerkar; Stephen S. Hecht
Chemical Research in Toxicology | 1991
Peter G. Foiles; Shobha A. Akerkar; Steven G. Carmella; Mark Kagan; Gary D. Stoner; James H. Resau; Stephen S. Hecht
Cancer Epidemiology, Biomarkers & Prevention | 1996
Stephen S. Hecht; Neil Trushin; Jeffrey Rigotty; Steven G. Carmella; Anna Borukhova; Shobha A. Akerkar; Abraham Rivenson
Chemical Research in Toxicology | 2002
Bogdan Prokopczyk; Dietrich Hoffmann; M Bologna; Aj Cunningham; Neil Trushin; Shobha A. Akerkar; Telih Boyiri; Shantu Amin; Dhimant Desai; Steven Colosimo; Brian Pittman; Gerd Leder; Marco Ramadani; Doris Henne-Bruns; Hans G. Beger; Karam El-Bayoumy
Cancer Epidemiology, Biomarkers & Prevention | 1998
William D. Parsons; Steven G. Carmella; Shobha A. Akerkar; Leo E. Bonilla; Stephen S. Hecht