Targeting TRPC6 channels in oesophageal carcinoma growth
- PMID: 20235901
- DOI: 10.1517/14728221003733602
Targeting TRPC6 channels in oesophageal carcinoma growth
Abstract
Importance of the field: Oesophageal carcinoma ranks among the ten most frequent cancers worldwide. The special growing site and malignant nature make it difficult to be completely treated by surgical operation and radiotherapy or chemotherapy. Discovery of new therapeutic targets responsible for the rapid proliferation of oesophageal carcinoma cells could help to treat this disease.
Areas covered in this review: Over the past two decades, studies have revealed a critical role of Ca(2+) channels in cancer cell proliferation. As non-selective cation channels, canonical transient receptor potential (TRPC) channels permeable to Ca(2+) are expressed in many types of tissues and are involved in the proliferation of cancer cells. The TRPC6 channel, a member of TRPC family, is highly expressed in oesophageal squamous cell carcinoma (OSCC) and is essential for cell proliferation and cell cycle. Inhibition of TRPC6 channels in human OSCC cells suppresses their proliferation and induces G2/M phase arrest.
What the reader will gain: In this review, we discuss the possible roles of TRPC6 channels and Ca(2+) signaling in OSCC cell proliferation.
Take home message: TRPC6 channels may be a novel therapeutic target for OSCC.
Similar articles
-
Critical role of TRPC6 channels in G2 phase transition and the development of human oesophageal cancer.Gut. 2009 Nov;58(11):1443-50. doi: 10.1136/gut.2009.181735. Epub 2009 Aug 2. Gut. 2009. PMID: 19651628
-
Essential role of TRPC6 channels in G2/M phase transition and development of human glioma.J Natl Cancer Inst. 2010 Jul 21;102(14):1052-68. doi: 10.1093/jnci/djq217. Epub 2010 Jun 16. J Natl Cancer Inst. 2010. PMID: 20554944
-
Blockade of TRPC6 channels induced G2/M phase arrest and suppressed growth in human gastric cancer cells.Int J Cancer. 2009 Nov 15;125(10):2281-7. doi: 10.1002/ijc.24551. Int J Cancer. 2009. PMID: 19610066
-
TRPC6: physiological function and pathophysiological relevance.Handb Exp Pharmacol. 2014;222:157-88. doi: 10.1007/978-3-642-54215-2_7. Handb Exp Pharmacol. 2014. PMID: 24756706 Review.
-
TRPC6.Handb Exp Pharmacol. 2007;(179):125-41. doi: 10.1007/978-3-540-34891-7_7. Handb Exp Pharmacol. 2007. PMID: 17217054 Review.
Cited by
-
PCC0208057 as a small molecule inhibitor of TRPC6 in the treatment of prostate cancer.Front Pharmacol. 2024 Mar 18;15:1352373. doi: 10.3389/fphar.2024.1352373. eCollection 2024. Front Pharmacol. 2024. PMID: 38567350 Free PMC article.
-
Store-Operated Calcium Channel Complex in Postsynaptic Spines: A New Therapeutic Target for Alzheimer's Disease Treatment.J Neurosci. 2016 Nov 23;36(47):11837-11850. doi: 10.1523/JNEUROSCI.1188-16.2016. J Neurosci. 2016. PMID: 27881772 Free PMC article.
-
How Dysregulated Ion Channels and Transporters Take a Hand in Esophageal, Liver, and Colorectal Cancer.Rev Physiol Biochem Pharmacol. 2021;181:129-222. doi: 10.1007/112_2020_41. Rev Physiol Biochem Pharmacol. 2021. PMID: 32875386 Review.
-
Zinc transporters and dysregulated channels in cancers.Front Biosci (Landmark Ed). 2017 Jan 1;22(4):623-643. doi: 10.2741/4507. Front Biosci (Landmark Ed). 2017. PMID: 27814637 Free PMC article. Review.
-
Pyrazolopyrimidines as Potent Stimulators for Transient Receptor Potential Canonical 3/6/7 Channels.J Med Chem. 2017 Jun 8;60(11):4680-4692. doi: 10.1021/acs.jmedchem.7b00304. Epub 2017 Apr 28. J Med Chem. 2017. PMID: 28395140 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous