CA
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVECOVER ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


CA Cancer J Clin 2003; 53:66
doi: 10.3322/canjclin.53.2.66
© 2003 American Cancer Society
This Article
Right arrow Full Text (PDF) Freely available
Right arrow Submit a letter to the editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Search for Related Content


NEWS & VIEWS

STUDY SUGGESTS NICOTINE MAY PROMOTE CANCER DEVELOPMENT

A report in the January 2003 issue of the Journal of Clinical Investigation (2003; 111:81–90) concludes that nicotine and its metabolite, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) may contribute to lung carcinogenesis by functioning as tumor promoters.


Figure
Nicotine may contribute to lung carcinogenesis.

Tobacco smoke contains over 40 known genotoxic initiators of carcino-genesis. The new information from this study suggests that nicotine and NNK inhibit apoptotic destruction of cells whose DNA has been damaged by these initiators, thereby allowing these cells the opportunity to persist and to undergo additional molecular changes eventuating in malignant transformation. In addition, exposure to these two compounds induced normal lung epithelial cell cultures to express two characteristics typical of malignant cells—a reduced dependence on growth factors and extracellular matrix, and an ability to continue growing under crowded conditions.

In their report, Phillip A. Dennis, PhD, and colleagues from the National Cancer Institute (NCI) in Bethesda, MD, and the Lovelace Respiratory Institute in Albuquerque, NM, also note previous studies indicating that nicotine might contribute to carcinogenesis via stimulation of angiogenesis. They conclude that, "...sustained exposure to nicotine might alter the phenotype of endothelial and/or epithelial cells in undetectable, premalignant lesions."

The significance of these observations is twofold. Firstly, description of this pathway as a component in lung carcinogenesis suggests it might be a target for chemopreventive or therapeutic agents. These observations also raise a second question that is of immediate clinical relevance; that is, whether nicotine replacement therapy (NRT) might contribute to carcinogenesis.

"This certainly is a valuable study, conducted by an excellent research team," said Thomas J. Glynn, PhD, National Director of Science and Trends at the American Cancer Society. "While well-conducted, [it] is preliminary and [this area] needs further investigation in order to unravel the complex puzzle of carcinogenesis." Addressing its relevance to NRT, Glynn said, "Continuing to smoke is far worse than any short-term exposure to nicotine through NRTs. As the authors themselves suggest, the most important action for a smoker to take is to quit, and nicotine replacement medications have proven effective in helping smokers do that."

In support of these conclusions, Glynn noted:

For these reasons, Glynn advises physicians to reassure their patients who are users of NRT. Although this information might help motivate some patients to wean themselves off NRT after they have been tobacco free, patients who are currently using NRT for tobacco cessation should NOT consider stopping the use of their medication.





This Article
Right arrow Full Text (PDF) Freely available
Right arrow Submit a letter to the editor
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Search for Related Content


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVECOVER ARCHIVE SEARCH TABLE OF CONTENTS