Enhanced expression of nicotinic alpha-1 acetylcholine receptor in lung cancer
K. Tanaka, W. Shuo, M. Takeshita, M. Izumi, K. Takayama, Y. Nakanishi (Fukuoka, Japan)
Source: Annual Congress 2010 - Pathology of lung cancer
Session: Pathology of lung cancer
Session type: Thematic Poster Session
Number: 3268
Disease area: Thoracic oncology
Abstract (Background) Nicotine, which is a major component of tobacco smoke, has been known as the principal psycoactive component to induce addiction by exerting its effects on the nicotinic acetylcholcholine receptors (nAchR) composed of alpha and beta subunits in the central nervous system. This addiction is thought to lead to the high incidence of the lung cancer through exposure to many carcinogens in the lung. Besides this, recent several reports suggested that nicotine might play another role in lung cancer by promoting in vivo the growth of cancer cells via nAcR signaling. nAchR exists in non-neural organs including lung. However, the precise mechanism how nicotine induces lung cancer remains to be elucidated. (Methods and results) To know expression profiles, we analyzed nAchR expression by immunohistochemistry in 24 Asian (Japanese) patients‘ specimen diagnosed as lung cancer (18 adenocarcinoma, 4 Squamous cell carcinoma, 1 large cell carcinoma and 1 small cell carcinoma) by Department of Pathology in Kyushu University. Interestingly, we found out that alpha 1 subunit was significantly expressed high in comparison to alpha 7 and other subunits. (Conclusions) Differnt from previous reports that alpha 7 might be important, we got an interesting result that alpha 1 would be also related to lung cancer. Each subunit in nAchR may have an essential and unique function in oncogenesis.
Rating:
You must login to grade this presentation.
Share or cite this content
Citations should be made in the following way:
K. Tanaka, W. Shuo, M. Takeshita, M. Izumi, K. Takayama, Y. Nakanishi (Fukuoka, Japan). Enhanced expression of nicotinic alpha-1 acetylcholine receptor in lung cancer. Eur Respir J 2010; 36: Suppl. 54, 3268
You must login to share this Presentation/Article on Twitter, Facebook, LinkedIn or by email.
Member's Comments
Related content which might interest you:
Related content which might interest you: