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MicroRNA in prostate cancer: functional importance and potential as circulating biomarkers.
- Source :
-
BMC cancer [BMC Cancer] 2014 Dec 10; Vol. 14, pp. 930. Date of Electronic Publication: 2014 Dec 10. - Publication Year :
- 2014
-
Abstract
- Background: This non-systematic review article aims to summarise the progress made in understanding the functional consequences of microRNA (miRNA) dysregulation in prostate cancer development, and the identification of potential miRNA targets as serum biomarkers for diagnosis or disease stratification.<br />Results: A number of miRNAs have been shown to influence key cellular processes involved in prostate tumourigenesis, including apoptosis-avoidance, cell proliferation and migration and the androgen signalling pathway. An overlapping group of miRNAs have shown differential expression in the serum of patients with prostate cancer of varying stages compared with unaffected individuals. The majority of studies thus far however, involve small numbers of patients and have shown variable and occasionally conflicting results<br />Conclusion: MiRNAs show promise as potential circulating biomarkers in prostate cancer, but larger prospective studies are required to validate particular targets and better define their clinical utility.
- Subjects :
- Androgens metabolism
Animals
Apoptosis genetics
Cell Movement genetics
DNA Methylation
Enhancer of Zeste Homolog 2 Protein
Gene Expression Regulation, Neoplastic
Humans
Male
MicroRNAs blood
Oncogene Proteins, Fusion genetics
Oncogene Proteins, Fusion metabolism
PTEN Phosphohydrolase metabolism
Polycomb Repressive Complex 2 metabolism
Prostatic Neoplasms blood
Prostatic Neoplasms diagnosis
Proto-Oncogene Proteins c-akt metabolism
Signal Transduction
Biomarkers, Tumor
MicroRNAs genetics
Prostatic Neoplasms genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1471-2407
- Volume :
- 14
- Database :
- MEDLINE
- Journal :
- BMC cancer
- Publication Type :
- Academic Journal
- Accession number :
- 25496077
- Full Text :
- https://doi.org/10.1186/1471-2407-14-930