CDC25 phosphatases as potential human oncogenes

Konstantin Galaktionov, Arthur K. Lee, Jens Eckstein, Giulio Draetta, Jason Meckler, Massimo Loda, David Beach

Research output: Contribution to journalArticlepeer-review

502 Scopus citations

Abstract

Cyclin-dependent kinases (CDKs) are activated by CDC25 phosphatases, which remove inhibitory phosphate from tyrosine and threonine residues. In human cells, CDC25 proteins are encoded by a multigene family, consisting of CDC25A, CDC25B, and CDC25C. In rodent cells, human CDC25A or CDC25B but not CDC25C phosphatases cooperate with either Ha-RAS(G12V) or loss of RB1 in oncogenic focus formation. Such transformants were highly aneuploid, grew in soft agar, and formed high-grade tumors in nude mice. Overexpression of CDC25B was detected in 32 percent of human primary breast cancers tested. The CDC25 phosphatases may contribute to the development of human cancer.

Original languageEnglish (US)
Pages (from-to)1575-1577
Number of pages3
JournalScience
Volume269
Issue number5230
StatePublished - Sep 15 1995
Externally publishedYes

ASJC Scopus subject areas

  • General

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