Literature DB >> 15032668

A rationale for inhibiting progesterone-related pathways to combat breast cancer.

Michael R Moore1.   

Abstract

Inhibitors of estrogen-related pathways have been used with some success in the treatment of breast cancer. These include the antiestrogens tamoxifen, more recently faslodex, and the aromatase inhibitor anastrazole. However, failure and recurrence rates are substantial with drugs countering the effects of estrogens. Progestins, unlike estrogens, have generally been considered to oppose breast cancer and have been used with reasonable efficacy after antiestrogen failure. However, a building body of evidence, from cell culture, animal studies, and, most recently, several major clinical studies involving hormone replacement therapy, strongly supports the notion that progestins generally stimulate breast cancer. Our studies and those of others suggest that progestins increase the numbers of breast cancer cells by both stimulating the rate of proliferation and inhibiting cell death. These data indicate that progestin-related pathways might provide effective targets for breast cancer therapy. This review addresses the rationale for using inhibitors of progestin-related pathways to treat breast cancer and comments on some possible points of attack.

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Year:  2004        PMID: 15032668     DOI: 10.2174/1568009043481515

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  3 in total

1.  Progestin stimulation of manganese superoxide dismutase and invasive properties in T47D human breast cancer cells.

Authors:  Aaron K Holley; Kelley K Kiningham; Douglas R Spitz; Dean P Edwards; Jeffrey T Jenkins; Michael R Moore
Journal:  J Steroid Biochem Mol Biol       Date:  2009-06-27       Impact factor: 4.292

2.  Membrane progesterone receptors (mPRs) mediate progestin induced antimorbidity in breast cancer cells and are expressed in human breast tumors.

Authors:  Gwen E Dressing; Rebecca Alyea; Yefei Pang; Peter Thomas
Journal:  Horm Cancer       Date:  2012-06       Impact factor: 3.869

3.  Phosphorylation of progesterone receptor serine 400 mediates ligand-independent transcriptional activity in response to activation of cyclin-dependent protein kinase 2.

Authors:  Lisa K Pierson-Mullany; Carol A Lange
Journal:  Mol Cell Biol       Date:  2004-12       Impact factor: 4.272

  3 in total

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