Abstract

Cutaneous melanoma is an aggressive neoplasm and is responsible for the majority of skin cancer deaths. Several miRNAs are involved in melanoma tumor progression. One of them is miR-205, the loss of which contributes to the development of melanoma metastasis. We evaluated whole-genome mRNA expression profiling associated with different miR-205 expression levels in melanoma cells. Differential expression analysis identified 243 differentially expressed transcripts including inositol polyphosphate 5′-phosphatase-like protein-1 (INPPL1) and BTB/POZ Domain-Containing Protein 3 (BTBD3). INPPL1 and BTBD3 were downregulated when melanoma cells expressed miR-205, indicating that these genes are potential miR-205 targets. Additionally, the target prediction algorithm TargetScan revealed that INPPL1 and BTBD3 genes had predicted target sites of miR-205 in their 3′UTRs and functional analysis demonstrated that these genes were directly linked to miR-205. Interestingly, our clinical data showed that INPPL1 was significantly associated with lymph node metastasis-free survival (LNMFS), distant metastasis-free survival (DMFS) and melanoma specific survival (MSS). This study supports INPPL1 as a miR-205 target gene and, therefore, that the involvement of miR-205 in the metastatic dissemination of malignant melanoma is, at least in part, via INPPL1.

Highlights

  • Most skin cancer related deaths are caused by melanoma, a malignant neoplasm with great potential to metastasize that is increasing in incidence and mortality[1]

  • With respect to age at diagnosis, the results revealed that inositol polyphosphate 5′-phosphatase-like protein-1 (INPPL1) and BTBD3 expression directly correlated with age (Spearman r 0.344, p 0.005; Spearman r 0.302, p 0.013 respectively) whilst ATF4 expression did not show any association with age (Fig. 6D)

  • Advances in the identification of the target genes for miR-205 may significantly contribute to delineating and understanding the molecular pathways involved in the metastatic dissemination of malignant melanoma when miR-205 expression is downregulated

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Summary

Introduction

Most skin cancer related deaths are caused by melanoma, a malignant neoplasm with great potential to metastasize that is increasing in incidence and mortality[1]. Epigenetic regulation of gene expression has, as in other cancer types, a significant role in melanoma[2]. Our aim was to clarify the targets and pathways by which miR-205 influences the development of metastasis in human cutaneous melanoma. For this purpose, we conducted a transcriptomic microarray-based profiling study in melanoma cells with and without miR-205 expression in order to analyze differences in gene expression and identify new genes targeted by miR-205 in melanoma

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