| Literature DB >> 26829037 |
Sen Guo1, Weinan Guo1, Shuli Li1, Wei Dai1, Nan Zhang1, Tao Zhao1, Huina Wang1, Jingjing Ma1, Xiuli Yi1, Rui Ge1, Gang Wang1, Tianwen Gao1, Chunying Li2.
Abstract
Melanoma is among the most malignant cancers with notorious aggressiveness, and its prognosis is greatly influenced by progression status. Serum microRNAs are small noncoding RNAs with high stability and easy accessibility in human blood. Their expression profiles are frequently dysregulated in cancers; hence, levels of serum microRNAs may reflect progression status and thus predict melanoma prognosis. In a hospital based case-control study, we found a significant reduction of serum miR-16 level in melanoma patients compared with cancer-free controls (P < 0.001). In addition, serum miR-16 level markedly decreased in melanoma patients with increased tumor thickness, occurrence of ulceration, and advanced American Joint Committee on Cancer stages, and was highly correlated with tissue Ki-67 expression (r = -0.521, P < 0.0001). Kaplan-Meier analysis and Cox proportional hazards regression analysis revealed a prognostic role of serum miR-16 (hazard ratio 2.49, 95% confidence interval 1.10-5.63, P = 0.028), which independently evaluated patients' survival outcome. Finally, the suppressive role of miR-16 in melanoma growth was validated both in vitro and in vivo. In conclusion, we demonstrated that serum miR-16 is a potential biomarker for predicting melanoma prognosis.Entities:
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Year: 2016 PMID: 26829037 DOI: 10.1016/j.jid.2015.12.041
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551