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Cell Volume Regulation in Epithelial Physiology and Cancer

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Journal Front Physiol
Date 2013 Sep 7
PMID 24009588
Citations 47
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Abstract

The physiological function of epithelia is transport of ions, nutrients, and fluid either in secretory or absorptive direction. All of these processes are closely related to cell volume changes, which are thus an integrated part of epithelial function. Transepithelial transport and cell volume regulation both rely on the spatially and temporally coordinated function of ion channels and transporters. In healthy epithelia, specific ion channels/transporters localize to the luminal and basolateral membranes, contributing to functional epithelial polarity. In pathophysiological processes such as cancer, transepithelial and cell volume regulatory ion transport are dys-regulated. Furthermore, epithelial architecture and coordinated ion transport function are lost, cell survival/death balance is altered, and new interactions with the stroma arise, all contributing to drug resistance. Since altered expression of ion transporters and channels is now recognized as one of the hallmarks of cancer, it is timely to consider this especially for epithelia. Epithelial cells are highly proliferative and epithelial cancers, carcinomas, account for about 90% of all cancers. In this review we will focus on ion transporters and channels with key physiological functions in epithelia and known roles in the development of cancer in these tissues. Their roles in cell survival, cell cycle progression, and development of drug resistance in epithelial cancers will be discussed.

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References
1.
Anbari K, Schultz R . Effect of sodium and betaine in culture media on development and relative rates of protein synthesis in preimplantation mouse embryos in vitro. Mol Reprod Dev. 1993; 35(1):24-8. DOI: 10.1002/mrd.1080350105. View

2.
Di Virgilio F . Purines, purinergic receptors, and cancer. Cancer Res. 2012; 72(21):5441-7. DOI: 10.1158/0008-5472.CAN-12-1600. View

3.
Nakahari T, Murakami M, Yoshida H, Miyamoto M, Sohma Y, Imai Y . Decrease in rat submandibular acinar cell volume during ACh stimulation. Am J Physiol. 1990; 258(6 Pt 1):G878-86. DOI: 10.1152/ajpgi.1990.258.6.G878. View

4.
Webb B, Chimenti M, Jacobson M, Barber D . Dysregulated pH: a perfect storm for cancer progression. Nat Rev Cancer. 2011; 11(9):671-7. DOI: 10.1038/nrc3110. View

5.
Shen M, Droogmans G, Eggermont J, Voets T, Ellory J, Nilius B . Differential expression of volume-regulated anion channels during cell cycle progression of human cervical cancer cells. J Physiol. 2000; 529 Pt 2:385-94. PMC: 2270206. DOI: 10.1111/j.1469-7793.2000.00385.x. View