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Philos Trans R Soc Lond B Biol Sci. 2014 Feb 3;369(1638):20130096. doi: 10.1098/rstb.2013.0096. Print 2014 Mar 19.

Role of anoctamins in cancer and apoptosis.

Author information

1
Institut für Physiologie, Universität Regensburg, , Universitätsstraße 31, Regensburg 93053, Germany.

Abstract

Anoctamin 1 (TMEM16A, Ano1) is a recently identified Ca(2+)-activated chloride channel and a member of a large protein family comprising 10 paralogues. Before Ano1 was identified as a chloride channel protein, it was known as the cancer marker DOG1. DOG1/Ano1 is expressed in gastrointestinal stromal tumours (GIST) and particularly in head and neck squamous cell carcinoma, at very high levels never detected in other tissues. It is now emerging that Ano1 is part of the 11q13 locus, amplified in several types of tumour, where it is thought to augment cell proliferation, cell migration and metastasis. Notably, Ano1 is upregulated through histone deacetylase (HDAC), corresponding to the known role of HDAC in HNSCC. As Ano1 does not enhance proliferation in every cell type, its function is perhaps modulated by cell-specific factors, or by the abundance of other anoctamins. Thus Ano6, by regulating Ca(2+)-induced membrane phospholipid scrambling and annexin V binding, supports cellular apoptosis rather than proliferation. Current findings implicate other cellular functions of anoctamins, apart from their role as Ca(2+)-activated Cl(-) channels.

KEYWORDS:

TMEM16A; TMEM16F; anoctamin 1; anoctamin 6; cancer; head and neck stromal cell carcinoma

PMID:
24493744
PMCID:
PMC3917350
DOI:
10.1098/rstb.2013.0096
[Indexed for MEDLINE]
Free PMC Article

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