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Differential expression of CDC25 phosphatases splice variants in human breast cancer cells
Author(s) -
Hélène Albert,
Susana Santos,
Eric Battaglia,
Miguel Brito,
N. Carolino,
Denyse Bagrel
Publication year - 2011
Publication title -
clinical chemistry and laboratory medicine (cclm)
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.977
H-Index - 103
eISSN - 1437-4331
pISSN - 1434-6621
DOI - 10.1515/cclm.2011.635
Subject(s) - cdc25 , cdc25a , breast cancer , biology , gene isoform , alternative splicing , splice , cancer research , cancer , kinase , gene , cell cycle , genetics , cyclin dependent kinase 1 , cell cycle checkpoint
CDC25 phosphatases control cell cycle progression by activating cyclin dependent kinases. The three CDC25 isoforms encoding genes are submitted to alternative splicing events which generate at least two variants for CDC25A and five for both CDC25B and CDC25C. An over-expression of CDC25 was reported in several types of cancer, including breast cancer, and is often associated with a poor prognosis. Nevertheless, most of the previous studies did not address the expression of CDC25 splice variants. Here, we evaluated CDC25 spliced transcripts expression in anti-cancerous drug-sensitive and resistant breast cancer cell lines in order to identify potential breast cancer biomarkers.

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