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Corticotropin Releasing Factor Receptors in breast cancer: Expression and activity in hormone-dependent growth in vitro
- Source :
- Peptides. 129
- Publication Year :
- 2019
-
Abstract
- Corticotropin Releasing Factor (CRF) neuropeptides coordinate the stress response via two distinct membrane receptors (CRF-Rs). We have previously shown expression of both CRF-Rs in human breast cancer tissues. In the present study, we examined in vitro using the MCF-7 cell line model, the regulation of CRF-Rs expression and their signaling in hormone-dependent breast cancer growth. Our findings show that similarly to breast cancer biopsies, the predominant receptor type expressed in the cell line is CRF-R2α. The transcription of CRF-R1 and CRF-R2 is up and down-regulated respectively by exposure to estradiol (E2); however this effect seems not to be exerted at the level of promoter gene methylation, although in human breast cancer specimens, CRF-R1 methylation was found to be positively associated with the presence of steroid hormone receptors. Finally, we showed that specific activation of CRF-R2 increased the migration of MCF-7 cells and potentiated an estrogen-inducing effect. Our data support an involvement of CRF-R signaling in breast cancer pathophysiology via a regulatory steroid-hormone interplay.
- Subjects :
- Adult
endocrine system
Physiology
medicine.drug_class
medicine.medical_treatment
Neuropeptide
Fluorescent Antibody Technique
030209 endocrinology & metabolism
Breast Neoplasms
Biology
Real-Time Polymerase Chain Reaction
Biochemistry
Polymerase Chain Reaction
Receptors, Corticotropin-Releasing Hormone
03 medical and health sciences
Cellular and Molecular Neuroscience
0302 clinical medicine
Endocrinology
Breast cancer
Cell surface receptor
Cell Movement
Cell Line, Tumor
medicine
Humans
Receptor
Aged
Cell Proliferation
Promoter
Middle Aged
medicine.disease
Steroid hormone
Estrogen
Cancer research
MCF-7 Cells
hormones, hormone substitutes, and hormone antagonists
030217 neurology & neurosurgery
Hormone
Subjects
Details
- ISSN :
- 18735169
- Volume :
- 129
- Database :
- OpenAIRE
- Journal :
- Peptides
- Accession number :
- edsair.doi.dedup.....820b93ad79d8e07e6a7d09a632665825