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Colocalisation of CD9 and mortalin in CD9-induced mitotic catastrophe in human prostate cancer cells.

Authors :
Zvereff, V.
Wang, J.-C.
Shun, K.
Lacoste, J.
Chevrette, M.
Source :
British Journal of Cancer. 10/8/2007, Vol. 97 Issue 7, p941-948. 8p. 2 Black and White Photographs, 3 Diagrams, 2 Charts.
Publication Year :
2007

Abstract

CD9, a member of the tetraspanin family of proteins, is involved in a variety of cellular interactions with many other proteins and molecules. Although CD9 has been implicated in cell fusion, migration and cancer progression, the detailed function of this protein is not completely understood and likely depends on interactions with different protein partners, which are not yet all known. Using co-immunoprecipitation and mass-spectrometric protein sequencing, we have identified in prostate cancer cells, a novel CD9 partner, the 75-kDa protein HSPA9B, also known as mortalin. We further show that introduction and overexpression of wild-type CD9 into human PC-3 prostate cancer cells induces mitotic catastrophe. We also demonstrate, by immunocolocalisation studies, the interaction of CD9 and mortalin in PC-3 cells undergoing mitotic catastrophe. Our results not only identified mortalin as a new CD9 partner, but also clarify the mechanisms by which CD9 may control prostate cancer progression.British Journal of Cancer (2007) 97, 941–948. doi:10.1038/sj.bjc.6603964 www.bjcancer.com Published online 11 September 2007 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
97
Issue :
7
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
26905435
Full Text :
https://doi.org/10.1038/sj.bjc.6603964