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Journal ArticleDOI

Tobacco-specific N-nitrosamines and Areca-derived N-nitrosamines : chemistry, biochemistry, carcinogenicity, and relevance to humans

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TLDR
Evidence is presented that strongly supports the concept that TSNA contribute to the increased risk for cancer of the upper digestive tract in tobacco chewers and for the increase risk of lung cancer, especially pulmonary adenocarcinoma, in smokers.
Abstract
Nicotine and the minor tobacco alkaloids give rise to tobacco-specific N-nitrosamines (TSNA) during tobacco processing and during smoking. Chemical-analytical studies led to the identification of seven TSNA in smokeless tobacco (< or = 25 micrograms/g) and in mainstream smoke of cigarettes (1.3 micrograms TSNA/cigarette). Indoor air polluted by tobacco smoke may contain up to 24 pg/L of TSNA. In mice, rats, and hamsters, three TSNA, N'-nitrosonornicotine (NNN), 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), and 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), are powerful carcinogens; two TSNA are moderately active as carcinogens; and two TSNA appear not to be carcinogenic. The TSNA are procarcinogens, agents that require metabolic activation. The active forms of the carcinogenic TSNA react with cellular components, including DNA, and with hemoglobin (Hb). The Hb adducts in chewers and smokers serve as biomarkers for the uptake and metabolic activation of carcinogenic TSNA and the urinary excretion of NNAL as free alcohol and as glucuronide for the uptake of TSNA. The review presents evidence that strongly supports the concept that TSNA contribute to the increased risk for cancer of the upper digestive tract in tobacco chewers and for the increased risk of lung cancer, especially pulmonary adenocarcinoma, in smokers. The high incidence of cancer of the upper digestive tract especially among men on the Indian subcontinent has been causally associated with chewing of betel quid mixed with tobacco. In addition to the TSNA, the betel quid chewers are exposed to four N-nitrosamines that are formed during chewing from the Areca alkaloids, two of these N-nitrosamines are carcinogens. The article also reviews approaches toward the reduction of the carcinogenic potency of smokeless tobacco, betel quid-tobacco mixtures, and cigarette smoke. Although the safest way to reduce the risk for tobacco-related cancers is to refrain from chewing and smoking, modifications of smokeless tobacco and of cigarettes are indicated to lead to less toxic products. Another more recent approach for reducing the carcinogenic effect of tobacco products is the application of chemopreventive agents, primarily of micronutrients. Future aspects in tobacco carcinogenesis, especially as it relates to TSNA, are expected in the field of molecular biochemistry and in biomarker studies, with the goal of identifying those tobacco and betel quid chewers and tobacco smokers who are at especially high risk for cancer.

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Patent

Tobacco products with reduced nicotine

TL;DR: In this paper, a plant quinolate phosphoribosyl transferase (QPRTase) enzyme was encoded in DNA and constructs comprising such DNA were provided, and methods of altering quinoline phosphorbi-biophase expression were provided.
Journal ArticleDOI

Re: Foulds and Ramstrom: Cancer Causes and Control 17: 227-228 (2006) and Henley et al., Cancer Causes and Control 16: 347-358 (2005). How smokeless tobacco can cause lung cancer.

TL;DR: Evidence is provided for a carcinogenic effect of smokeless tobacco first suggested by D. Hoffmann and I more than 15 years ago and repeatedly discussed—the occurrence of lung cancer in smokeless Tobacco users due to the presence in these products of sizeable amounts of the systemic lung carcinogen NNK.
Dissertation

Predicting the outcome of oral potentially malignant disorders using a composite clinical, histopathological and molecular classifier

TL;DR: The author states that the aim of this book is to provide a history of oral cancer in the context of modern medicine and to contribute to the public understanding of this disease.
Journal ArticleDOI

Hair nicotine concentration of cats with gastrointestinal lymphoma and unaffected control cases.

TL;DR: A significant association was not identified between HNC (a biomarker for ETS) and gastrointestinal lymphoma in cats; however, an association may exist and further studies are therefore required.
Journal ArticleDOI

A Quantitative Real-Time PCR-Based Strategy for Molecular Evaluation of Nicotine Conversion in Burley Tobacco

TL;DR: A novel strategy based on quantitative real-time polymerase chain reaction (qPCR) method is reported, which analyzed the ratio of nicotine conversion through examining the transcript level of CYP82E4 in burley leaves and do not need ethylene induction before detected.
References
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Journal Article

Smoking and Drinking in Relation to Oral and Pharyngeal Cancer

TL;DR: Risks of oropharyngeal cancer tended to combine more in a multiplicative than additive fashion and were increased more than 35-fold among those who consumed two or more packs of cigarettes and more than four alcoholic drinks/day.
Journal ArticleDOI

Smoking and health.

C. M. Fletcher, +1 more
- 01 Aug 1970 - 
TL;DR: Evidence connecting smoking with disease smoking habits and total mortality diseases causing excess mortality of cigarette smokers cigarette smoking as a cause of excess mortality specific diseases related to cigarette smoking approaches to prevention and experience in the United States.
Journal ArticleDOI

The Production of Malignant Primary Hepatic Tumours in the Rat by Feeding Dimethylnitrosamine

TL;DR: ImagesFigs.
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