| Literature DB >> 33099468 |
Ulrich H Weidle1, Simon AuslÄnder2, Ulrich Brinkmann1.
Abstract
During the last years a considerable therapeutic progress in melanoma patients with the RAF V600E mutation via RAF/MEK pathway inhibition and immuno-therapeutic modalities has been witnessed. However, the majority of patients relapse after therapy. Therefore, a deeper understanding of the pathways driving oncogenicity and metastasis of melanoma is of paramount importance. In this review, we summarize microRNAs modulating tumor growth, metastasis, or both, in preclinical melanoma-related in vivo models and possible clinical impact in melanoma patients as modalities and targets for treatment of melanoma. We have identified miR-199a (ApoE, DNAJ4), miR-7-5p (RelA), miR-98a (IL6), miR-219-5p (BCL2) and miR-365 (NRP1) as possible targets to be scrutinized in further target validation studies. CopyrightEntities:
Keywords: Epithelial-mesenchymal transition; invasion and proliferation; metastasis models; microRNA editing; microRNA inhibition and reconstitution of function; migration; review; therapeutic targets
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Year: 2020 PMID: 33099468 PMCID: PMC7675655 DOI: 10.21873/cgp.20221
Source DB: PubMed Journal: Cancer Genomics Proteomics ISSN: 1109-6535 Impact factor: 4.069