MiR-455-5p Suppresses the Progression of Prostate Cancer by Targeting CCR5.
Qianwei XingHuyang XieBingye ZhuZhiwei SunYe-Qing HuangPublished in: BioMed research international (2019)
Accumulated evidence indicates that miR-455-5p functions as tumor suppressor in the progression of various cancers. However, the mechanism through which miR-455-5p influences the tumorigenesis of human prostate cancer (PCa) remains undetermined. In this study, reanalysis of data obtained from the Memorial Sloan Kettering Cancer Center showed that miR-455-5p can be used as biomarker for PCa diagnosis and predictor of poor prognosis. Functional assays indicated that miR-455-5p overexpression could suppress cellular proliferation, inhibit tumor growth, and trigger apoptosis by activating and cleaving caspase 3. We experimentally verified that miR-455-5p negatively regulated the C-C motif chemokine receptor 5 (CCR5). Overall, our data demonstrate that miR-455-5p suppressed PCa cellular proliferation and induced cell apoptosis by downregulating CCR5. Thus, miR-455-5p may be considered a new therapeutic strategy for PCa.
Keyphrases
- prostate cancer
- poor prognosis
- signaling pathway
- radical prostatectomy
- dendritic cells
- long non coding rna
- regulatory t cells
- cell death
- electronic health record
- cell proliferation
- induced apoptosis
- endothelial cells
- transcription factor
- big data
- oxidative stress
- papillary thyroid
- pi k akt
- endoplasmic reticulum stress
- cell cycle arrest
- diabetic rats
- high throughput
- squamous cell
- childhood cancer
- immune response
- pluripotent stem cells
- young adults
- drug induced
- artificial intelligence