Identification of a functional polymorphism within the 3′-untranslated region of denticleless E3 ubiquitin protein ligase homolog associated with survival in acral melanoma

• DOI: 10.1016/j.ejca.2019.06.006
• Publication Date: 2019-07-17T18:10:10Z
• Authors: Lu Yang; Jie Dai; Meng Ma; Lili Mao; Lu Si; Chuanliang Cui; Xinan Sheng; Zhihong Chi; Sifan Yu; Tianxiao Xu; Jinyu Yu; Yan Kong; Jun Guo
• Keywords: Adult; Male; 0303 health sciences; Binding Sites; Nuclear Proteins; Middle Aged; Polymorphism, Single Nucleotide; Gene Expression Regulation, Enzymologic; Progression-Free Survival; Gene Expression Regulation, Neoplastic; MicroRNAs; 03 medical and health sciences; HEK293 Cells; Phenotype; Humans; Female; Genetic Predisposition to Disease; RNA Processing, Post-Transcriptional; 3' Untranslated Regions; Melanoma; Aged; Retrospective Studies

High expression of denticleless E3 ubiquitin protein ligase homologue (DTL) correlates with poor disease-free survival and overall survival in cutaneous melanoma, but the molecular features and clinical significance of this gene in acral melanoma (AM) remain unclear.The expression levels of DTL were compared between AM and benign melanocytic nevi using existing Gene Expression Omnibus data and validated in fresh frozen tissues. Two candidate tag single-nucleotide polymorphisms (SNPs) in the 3'-untranslated region (3'UTR) of DTL in patients with AM were sequenced and analysed for their association with survival in a discovery cohort (n = 570), and the significant SNP was subjected to a replication cohort (n = 201). The expression of DTL was evaluated by immunohistochemistry. The microRNA interacting with rs11275300:C > G was predicted using in silico target prediction tools and validated by in vitro analysis.DTL was overexpressed in AM compared with benign melanocytic nevi. rs11275300:C > G was found to be significantly associated with progression-free survival and overall survival of patients with AM in both cohorts and the combined cohort. Furthermore, the DTL expression level in the patients with the rs11275300:G allele was higher than that in patients with the CC genotype. In vitro analysis demonstrated that DTL was a direct target of hsa-miR-4672, and the rs11275300:G allele interfered with the binding affinity of hsa-miR-4672 with the 3'UTR of DTL and thereby increased DTL expression.The rs11275300:G allele in the 3'UTR of DTL may lead to a poor prognosis and allele-specific increase in the expression of DTL by post-transcriptional regulation in AM.