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MicroRNA-221 and -222 pathway controls melanoma progression

期刊

EXPERT REVIEW OF ANTICANCER THERAPY
卷 8, 期 11, 页码 1759-1765

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TAYLOR & FRANCIS LTD
DOI: 10.1586/14737140.8.11.1759

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antagomir; c-KIT; melanoma; microRNA; p27Kip; tumor progression

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  1. Italian Ministry of Health to Alessandra Car

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MicroRNAs (miRNAs) represent a new family of small noncoding RNAs that negatively regulate gene expression. Recent studies demonstrated miRNA involvement in all the main biological processes, including tumor development as a consequence of an aberrant deregulated expression. Growing evidence is showing the capability of miRNA expression profiles to unequivocally distinguish between normal and neoplastic tissues, leading to the identification of new diagnostic and/or prognostic molecular markers. In addition, miRNAs might eventually represent new targets to aim at as innovative therapeutic approaches, particularly relevant in those types of cancer, such as melanoma, which are still lacking effective traditional therapies. In particular, the inhibition of miRNA-221 and -222, which are abnormally expressed in melanoma and favor the induction of the malignant phenotype by downregulating c-KIT receptor and p27Kip, might in the future represent an efficient treatment for translation into the clinical setting.

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