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PGRMC1 (progesterone receptor membrane component 1): A targetable protein with multiple functions in steroid signaling, P450 activation and drug binding

期刊

PHARMACOLOGY & THERAPEUTICS
卷 121, 期 1, 页码 14-19

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pharmthera.2008.09.006

关键词

Progesterone; P450 proteins; Cholesterol; Carcinogenicity; Chemotherapy

资金

  1. American Cancer Society [85-001-19-IRG]
  2. NIH [COBRE P20 RR 15592]
  3. BIRCVVH (Building Interdisciplinary Research Careers in Women's Health) [K12DA 14040-06]
  4. NATIONAL CENTER FOR RESEARCH RESOURCES [P20RR015592] Funding Source: NIH RePORTER
  5. NATIONAL INSTITUTE ON DRUG ABUSE [K12DA014040] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Hormone signaling is important in a number of disease states, and hormone receptors are effective therapeutic targets. PGRMC1 (progesterone receptor membrane component 1) is a member of a multi-protein complex that binds to progesterone and other steroids, as well as pharmaceutical compounds. In spite of its name, PGRMC1 shares homology with cytochrome b(5)-related proteins rather than hormone receptors, and heme binding is the sole biochemical activity of PGRMC1. PGRMC1 and its homologues regulate cholesterol synthesis by activating the P450 protein Cyp51/lanosterol demethylase, and the cholesterol synthetic pathway is an important target in cardiovascular disease and in treating infections. PGRMC1 binding partners include multiple P450 proteins, PAIR-BP1, Insig, and an uncharacterized hormone/drug-binding protein. PGRMC1 is induced in a spectrum of cancers, where it promotes cell survival and damage resistance, and PGRMC1 is also expressed in the nervous system and tissues involved in drug metabolism, cholesterol synthesis and hormone synthesis and turnover. One of the appealing features of PGRMC1 and its associated protein complex is its affinity for steroids and drugs. Together with its biological role in promoting tumor survival, PGRMC1 is an attractive target for therapeutic intervention in cancer and related malignancies. (c) 2008 Elsevier Inc. All rights reserved.

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