Abstract |
Progesterone receptor membrane components 1 and 2, neudesin, and neuferricin belong to the membraneassociated progesterone receptor (MAPR) family. Recently, sex steroid membrane receptors have gained attention because of their potential involvement in sex hormone-mediated rapid non-genomic effects, which cannot currently be explained by the genomic action of nuclear receptors. Progesterone may increase cell proliferation and survival via nongenomic effects including the activation of the mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3- kinase (PI3K) pathways through MAPRs. Moreover, the unique expression of MAPRs suggests that they could be used as biomarkers and drug targets for sex steroid-related cancers and other diseases. In this review, we summarize the physiological roles of the MAPRs, provide a comprehensive overview of their progesterone-mediated non-genomic actions, and discuss new insights into their potential as therapeutic targets.
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Authors | Sae Hasegawa, Mayu Kasubuchi, Kazuya Terasawa, Ikuo Kimura |
Journal | Current drug targets
(Curr Drug Targets)
Vol. 17
Issue 10
Pg. 1189-97
( 2016)
ISSN: 1873-5592 [Electronic] United Arab Emirates |
PMID | 25981602
(Publication Type: Journal Article, Review, Research Support, Non-U.S. Gov't)
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Chemical References |
- Gonadal Steroid Hormones
- Receptors, Progesterone
- Progesterone
- Phosphatidylinositol 3-Kinases
- Mitogen-Activated Protein Kinases
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Topics |
- Animals
- Cell Proliferation
(physiology)
- Drug Design
- Gonadal Steroid Hormones
(metabolism)
- Humans
- Mitogen-Activated Protein Kinases
(metabolism)
- Molecular Targeted Therapy
- Neoplasms
(drug therapy, pathology)
- Phosphatidylinositol 3-Kinases
(metabolism)
- Progesterone
(metabolism)
- Receptors, Progesterone
(metabolism)
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