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A Robust Discovery Platform for the Identification of Novel Mediators of Melanoma Metastasis
Published on: March 8, 2022
The pleiotropic roles of circular and long noncoding RNAs in cutaneous melanoma
Barbara Montico1, Giorgio Giurato2,3, Giovanni Pecoraro2,3
1Immunopathology and Cancer Biomarkers, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, Italy.
Abstract:
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 BRAFV600 mutations in approximately 50% of CM patients has recently fueled the development of novel small-molecule inhibitors that specifically target BRAFV600 -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 BRAFV600 -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.
Insights
Circular RNAs (circRNAs) and long noncoding RNAs (lncRNAs) play key roles in cutaneous melanoma (CM) development and treatment resistance. Understanding these noncoding RNAs offers new avenues for BRAF-mutant CM targeted therapy and immunotherapy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Cutaneous melanoma (CM) is an aggressive skin cancer with high mortality.
- BRAF V600 mutations are found in ~50% of CM patients, driving targeted therapy development.
- Noncoding RNAs (ncRNAs), including microRNAs, circular RNAs (circRNAs), and long noncoding RNAs (lncRNAs), are increasingly implicated in CM.
Purpose of the Study:
- To review the molecular functions of circRNAs and lncRNAs in BRAF V600-mutant CM.
- To explore the role of circRNAs and lncRNAs in CM immunogenicity and treatment resistance.
- To evaluate computational tools for circRNA and lncRNA functional interaction prediction.
Main Methods:
- Literature review and critical analysis of existing studies on circRNAs and lncRNAs in CM.
- Focus on BRAF V600-mutant CM, targeted therapy, and immunotherapy resistance.
- Evaluation of bioinformatics algorithms and databases for ncRNA analysis.
Main Results:
- Aberrant expression of circRNAs and lncRNAs is evident in CM.
- These ncRNAs influence CM pathogenesis, targeted therapy response, and immunotherapy resistance.
- Evidence suggests circRNAs and lncRNAs modulate CM immunogenicity.
Conclusions:
- circRNAs and lncRNAs represent promising biomarkers and therapeutic targets in CM.
- Further research is needed to fully elucidate their roles in BRAF-mutant CM and immune evasion.
- Computational tools are crucial for understanding circRNA and lncRNA functional networks.
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