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.

Molecular Oncology
|June 3, 2021
PubMed

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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