DocumentCode
3149477
Title
Mecamylamine affects cell proliferation and adhesion of lung cancer in vitro
Author
Ma, Xiaoli ; Zhao, Yun ; Wang, Yunshan ; Zhang, Xiuping ; Zhou, Qian ; Sun, Haiji ; An, Liguo ; Zhang, Xueping
Author_Institution
Med. Res. & Lab. Diagnostic Center, Jinan Central Hosp. Affiliated to Shandong Univ., Jinan, China
Volume
5
fYear
2010
fDate
16-18 Oct. 2010
Firstpage
2078
Lastpage
2080
Abstract
Mecamylamine, pharmacologically, has been well characterized as a nonselective and noncompetitive antagonist of nicotinic acetylcholine receptors (nAChRs). Because mecamylamine easily crosses the blood - brain barrier at relatively low doses, it has been used by several research groups over the past two decades investigating the role of central nAChRs in the etiology and treatment of various neuropsychiatric disorders. Recently, nAChRs have also been found on non-neuronal cells such as bronchial epithelium and keratinocytes, so it is necessary to investigate the antitumor activity of mecamylamine in lung cancer. In the present study, we study the effects of mecamylamine on cell proliferation and adhesion of lung cancer in vitro. The results showed that cell proliferation of lung cancer was inhibited by mecamylamine treatment in dose dependent and time dependent manners and expression of cell adhesion molecule was changed after mecamylamine treatment. These results indicate that nAChRs played important roles in cell proliferation as well as cell adhesion of lung cancer and action of mecamylamine may be effective as an augmentation pharmacotherapy for lung cancer.
Keywords
biochemistry; cancer; cellular biophysics; lung; patient treatment; pharmaceuticals; bronchial epithelium; cell adhesion; cell proliferation; keratinocytes; lung cancer augmentation pharmacotherapy; mecamylamine antitumor activity; nicotinic acetylcholine receptor; noncompetitive nAChR antagonist; nonselective nAChR antagonist; Adhesives; Biomembranes; Cancer; Computer architecture; Genomics; Lungs; Microprocessors; adhesion; cell proliferation; lung cancer; mecamylamine; nicotinic acetylcholine receptors;
fLanguage
English
Publisher
ieee
Conference_Titel
Biomedical Engineering and Informatics (BMEI), 2010 3rd International Conference on
Conference_Location
Yantai
Print_ISBN
978-1-4244-6495-1
Type
conf
DOI
10.1109/BMEI.2010.5639870
Filename
5639870
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