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March 3, 2026Frontiers in Molecular Biosciences3 citationsOpen Access

Non-coding RNA transcripts and their exosomal counterparts in the pathogenesis, diagnosis, and treatment of skin cancers, with a focus on melanoma

LZLinjing ZouXWXuemei WenFujian Medical UniversityXDXiyan Dai

Key Points

  • Melanoma remains a serious threat due to challenges like tumor recurrence and drug resistance, highlighting the need for better strategies.
  • The study emphasizes the critical role of non-coding RNAs in regulating key processes like immune response and treatment resistance.
  • Reviewing current studies on ncRNAs and exosomes provides insights into their potential as diagnostic and therapeutic targets.
  • Understanding these components may offer novel pathways for improving treatment efficacy in skin cancers, particularly melanoma.

Abstract

Skin malignancies, including melanoma and non-melanoma cancers, are the most common cancers worldwide, with increasing incidence and fatality rates. Malignant melanoma (MM) is a highly aggressive cancer with poor prognosis, and despite various therapies, it remains a serious threat due to factors like tumor recurrence, drug resistance, and lack of effective treatments. Non-coding RNAs (ncRNAs) transcripts have gained attention due to their critical roles in regulating proliferation, angiogenesis, immune regulation, invasion, metastasis, and treatment resistance. Exosomes, biologically active lipid-bilayer extracellular vesicles secreted by various cell types, are also involved in cancer by carrying multiple bioactive molecules, including ncRNAs. Investigating the noncoding components of the transcriptome and their exosomal counterparts opens up the possibility of discovering new therapeutic and diagnostic targets. This review discusses current studies on the involvement of ncRNAs and their exosomal counterparts in the pathogenesis, diagnosis, and treatment of human skin cancers, particularly melanoma.

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Cite This Study

Zou et al. (2026) studied this question.

synapsesocial.com/papers/69a75e31c6e9836116a289c8https://doi.org/10.3389/fmolb.2026.1669297
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