Abstract
UHRF1 promotes melanoma progression by inducing cell proliferation, and is correlated with poor prognosis of melanoma patients. However, the regulation mechanism has not been fully elaborated. Here, we detected hsa-let-7b expression and its role in melanoma. Through Targetscan and miRanda predication, 30 overlapped miRNAs were found; further survival analysis revealed that hsa-let-7b was the only miRNA that affected the overall survival. Overexpressed hsa-let-7b could significantly inhibit the proliferation ability of A375 and A2058 cells, and this phenomenon was reversed after co-transfection with pLenti-UHRF1. In conclusion, hsa-let-7b regulates melanoma cells proliferation in vitro by targeting UHRF1.
Acknowledgments
The authors thank the Pathology Department of Zhongshan Hospital for providing tumor samples.
Ethics approval and consent to participate
Ethical approval for the study was obtained from the Ethics Committee of the Zhongshan Hospital Biomedical Research, and written informed consent was obtained from each patient.
Authors’ contributions
GJY and QFZ conceived and designed the study. LNH and WCY performed the experiments. LNH wrote the manuscript. WCY reviewed and edited the manuscript. All authors read and approved the manuscript and agree to be accountable for all aspects of the research in ensuring that questions about the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Disclosure statement
The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the article.
Availability of data and materials
The datasets used in the present study are available from the corresponding author upon reasonable request.