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Implication of β2-adrenergic receptor and miR-196a correlation in neurite outgrowth of LNCaP prostate cancer cells.
- Source :
-
PloS one [PLoS One] 2021 Jun 30; Vol. 16 (6), pp. e0253828. Date of Electronic Publication: 2021 Jun 30 (Print Publication: 2021). - Publication Year :
- 2021
-
Abstract
- The β2-adrenergic receptor has been shown to be involved in neuroendocrine differentiation and to contribute to the development of aggressive prostate cancer. In this study we have investigated whether miR-196a plays a role in the regulation of the β2-adrenergic receptor in the LNCaP prostate cancer cell line. Our results show that the expression of miR-196a is elevated in LNCaP prostate cancer cells with reduced levels of β2-adrenergic receptor after stably transfection with three different shRNAs. Furthermore, treatment with β-blockers showed that this upregulation is strictly related to the low levels of β2-adrenergic receptor and not to the inhibition of the receptor signaling activity. Finally, we found that the reduced ability of LNCaP cells with low levels of β2-adrenergic receptor to initiate neuroendocrine differentiation under androgen depletion conditions is mediated by miR-196a. In conclusion, this study provides the rational for a role of miR-196a in the β2-adrenergic receptor mediated neuroendocrine differentiation of LNCaP prostate cancer cells.<br />Competing Interests: The authors have declared that no competing interests exist.
- Subjects :
- Adrenergic beta-2 Receptor Antagonists
Cell Line, Tumor
Gene Knockdown Techniques
Humans
Male
MicroRNAs genetics
Neuronal Outgrowth drug effects
Prostate pathology
Prostatic Neoplasms pathology
Receptors, Adrenergic, beta-2 metabolism
Up-Regulation
Gene Expression Regulation, Neoplastic
MicroRNAs metabolism
Neuronal Outgrowth genetics
Prostatic Neoplasms genetics
Receptors, Adrenergic, beta-2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1932-6203
- Volume :
- 16
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- PloS one
- Publication Type :
- Academic Journal
- Accession number :
- 34191854
- Full Text :
- https://doi.org/10.1371/journal.pone.0253828