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Nicotinic acetylcholine receptors in cancer: multiple roles in proliferation and inhibition of apoptosis.

Abstract
Nicotinic acetylcholine receptors (nAChRs) constitute a heterogeneous family of ion channels that mediate fast synaptic transmission in neurons. They have also been found on non-neuronal cells such as bronchial epithelium and keratinocytes, underscoring the idea that they have functions well beyond neurotransmission. Components of cigarette smoke, including nicotine and NNK [4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone], are agonists of nAChRs. Given the association of tobacco use with several diseases, the non-neuronal nAChR signaling pathway has considerable implications for cancer and cardiovascular disease. Recent studies have shown that alpha7 is the main nAChR subunit that mediates the proliferative effects of nicotine in cancer cells. As a result, alpha7 nAChR might be a valuable molecular target for therapy of cancers such as lung cancer and mesothelioma. Future studies involving the design of nAChR antagonists with improved selectivity might identify novel strategies for the treatment of tobacco-related cancers. Here we review the cellular roles of non-neuronal nAChRs, including regulation of cell proliferation, angiogenesis, apoptosis, migration, invasion and secretion.
AuthorsRichard D Egleton, Kathleen C Brown, Piyali Dasgupta
JournalTrends in pharmacological sciences (Trends Pharmacol Sci) Vol. 29 Issue 3 Pg. 151-8 (Mar 2008) ISSN: 0165-6147 [Print] England
PMID18262664 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S., Review)
Chemical References
  • Nitrosamines
  • Receptors, Nicotinic
  • Nicotine
Topics
  • Animals
  • Apoptosis (drug effects)
  • Cell Proliferation (drug effects)
  • Humans
  • Neoplasms (blood supply, drug therapy, metabolism, pathology)
  • Neovascularization, Pathologic (chemically induced, metabolism)
  • Nicotine (toxicity)
  • Nitrosamines (toxicity)
  • Receptors, Nicotinic (biosynthesis, metabolism)
  • Signal Transduction (drug effects)
  • Nicotiana (adverse effects, chemistry)

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