The pleiotropic role of circular and long noncoding RNAs in cutaneous melanoma

被引:16
作者
Montico, Barbara [1 ]
Giurato, Giorgio [2 ,3 ]
Pecoraro, Giovanni [2 ,3 ]
Salvati, Annamaria [2 ]
Covre, Alessia [4 ,5 ]
Colizzi, Francesca [1 ]
Steffan, Agostino [1 ]
Weisz, Alessandro [2 ,3 ]
Maio, Michele [4 ,5 ,6 ]
Sigalotti, Luca [7 ]
Fratta, Elisabetta [1 ]
机构
[1] IRCCS, Ctr Riferimento Oncol Aviano CRO, Immunopathol & Canc Biomarkers, Via Franco Gallini 2, I-33081 Aviano, PN, Italy
[2] Univ Salerno, Scuola Med Salernitana, Dept Med Surg & Dent, Lab Mol Med & Genom, Via S Allende, I-84081 Baronissi, SA, Italy
[3] Univ Salerno, Genome Res Ctr Hlth CRGS, Campus Med, Baronissi, Italy
[4] Univ Hosp Siena, Ctr Immunooncol, Siena, Italy
[5] Univ Siena, Siena, Italy
[6] NIBIT Fdn Onlus, Siena, Italy
[7] IRCCS, Ctr Riferimento Oncol Aviano CRO, Oncogenet & Funct Oncogenom Unit, Aviano, Italy
关键词
circular RNAs; cutaneous melanoma; immunotherapy; long noncoding RNAs; targeted therapy; MANUALLY CURATED DATABASE; COMPETING ENDOGENOUS RNA; CELL-PROLIFERATION; MALIGNANT-MELANOMA; MAPK PATHWAY; TUMOR-GROWTH; MESENCHYMAL TRANSITION; METASTATIC MELANOMA; GLUCOSE-METABOLISM; OXIDATIVE STRESS;
D O I
10.1002/1878-0261.13034
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cutaneous melanoma (CM) is a very aggressive disease, often characterized by unresponsiveness to conventional therapies and high mortality rates worldwide. The identification of the activating BRAF(V600) mutations in approximately 50% of CM patients has recently fueled the development of novel small-molecule inhibitors that specifically target BRAF(V600)-mutant CM. In addition, a major progress in CM treatment has been made by monoclonal antibodies that regulate the immune checkpoint inhibitors. However, although target-based therapies and immunotherapeutic strategies have yielded promising results, CM treatment remains a major challenge. In the last decade, accumulating evidence points to the aberrant expression of different types of noncoding RNAs (ncRNAs) in CM. While studies on microRNAs have grown exponentially leading to significant insights on CM biology, the role of circular RNAs (circRNAs) and long noncoding RNAs (lncRNAs) in this tumor is less understood, and much remains to be discovered. Here, we summarize and critically review the available evidence on the molecular functions of circRNAs and lncRNAs in BRAF(V600)-mutant CM and CM immunogenicity, providing recent updates on their functional role in targeted therapy and immunotherapy resistance. In addition, we also include an evaluation of several algorithms and databases for prediction and validation of circRNA and lncRNA functional interactions.
引用
收藏
页码:565 / 593
页数:29
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