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  • Original Paper
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Increased susceptibility to carcinogen-induced mammary tumors in MMTV-Cdc25B transgenic mice

Abstract

Cdc25 phosphatases activate cyclin-dependent kinases (Cdks) by dephosphorylating critical phospho-tyrosine and phospho-threonine residues on these proteins. Several types of studies indicate that Cdc25s can enhance cell proliferation and oncogenesis. Furthermore, overexpression of Cdc25A and/or B have been detected in several types of primary human cancers, including breast cancers. To further assess the oncogenic capacity of Cdc25B in vivo, we have generated transgenic mice that overexpress Cdc25B in the mammary epithelium, driven by the MMTV – LTR promoter. Although these mice are grossly normal for up to 18 months, the ectopic expression of Cdc25B in their mammary glands increases the susceptibility of these mice to induction of mammary tumors by the carcinogen 9,10-dimethyl-1,2-benzanthracene (DMBA).

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Acknowledgements

We are grateful for the excellent administrative assistance provided by Barbara Castro. We thank Dr David Beach for the Cdc25B2 cDNA and Dr Giorgio Cattoretti for technical assistance and helpful discussions. This work was supported by National Institutes of Health Grant RO1 CA/ES 63467, and an award from the National Foundation for Cancer Research (to Dr I Bernard Weinstein). ED Slosberg was supported by NCI Cancer Training Grant T32CA09503 and a NIH Pre-Doctoral Training Grant T32GM07088.

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Yao, Y., Slosberg, E., Wang, L. et al. Increased susceptibility to carcinogen-induced mammary tumors in MMTV-Cdc25B transgenic mice. Oncogene 18, 5159–5166 (1999). https://doi.org/10.1038/sj.onc.1202908

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