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Volume-sensitive organic osmolyte/anion channels in cancer: novel approaches to studying channel modulation employing proteomics technologies.
- Source :
-
Annals of the New York Academy of Sciences [Ann N Y Acad Sci] 2004 Dec; Vol. 1028, pp. 38-55. - Publication Year :
- 2004
-
Abstract
- Key elements of tumor development include proliferation, migration, invasiveness, and angiogenesis. Activation of the volume-sensitive organic osmolyte/anion channel (VSOAC) has been suggested to play a role in all of these processes. VSOACs may therefore represent an important therapeutic target in the etiology of cancer. However, pharmacological inhibitors of VSOAC are nonselective and of low potency, highlighting the importance of identifying novel regulators of the channel. The use of electrophysiological methods coupled with techniques such as pull-down assays, yeast 2-hybrid, and functional protein arrays have already proved valuable in studying protein-protein interactions in a variety of systems. Some of these methods have been used to identify small molecules that modulate the function of other types of ion channels. Given that several proteins have already been identified as putative modulators of VSOACs, proteomics technologies may prove useful in elucidating the molecular identity of VSOACs and helpful in identifying novel modulators of channel function. In this paper, we review the involvement of VSOACs in tumor development processes and its regulation by pharmacological agents and cellular proteins. Proteomic approaches to study protein-protein interactions and how such approaches may be used to study VSOACs are also discussed. We speculate on how modulation of protein-protein interactions may result in the identification of a novel class of compounds for modulating VSOACs.
- Subjects :
- Animals
Anions
Binding Sites
Cell Cycle
Cell Line, Tumor
Cell Movement
Cell Proliferation
Dogs
Dose-Response Relationship, Drug
Drug Design
Electrophysiology
HeLa Cells
Humans
Ion Channels chemistry
Ions chemistry
Neoplasm Invasiveness
Neovascularization, Pathologic
Protein Binding
Proteins chemistry
Rats
Two-Hybrid System Techniques
Culture Techniques
Neoplasms metabolism
Proteomics methods
Subjects
Details
- Language :
- English
- ISSN :
- 0077-8923
- Volume :
- 1028
- Database :
- MEDLINE
- Journal :
- Annals of the New York Academy of Sciences
- Publication Type :
- Academic Journal
- Accession number :
- 15650230
- Full Text :
- https://doi.org/10.1196/annals.1322.004