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Updated: Apr 16, 2026

Analysis of Lymph Node Volume by Ultra-High-Frequency Ultrasound Imaging in the Braf/Pten Genetically Engineered Mouse Model of Melanoma
Published on: September 8, 2021
Insight into the emerging role of long non-coding RNAs in BRAF inhibitor resistance in melanoma
Vikas Yadav1, Manoj Kumar Jena2, Tejveer Singh3
1Department of Translational Medicine, Clinical Research Centre, Skåne University Hospital, Lund University, Malmö, Sweden.
Abstract:
Melanoma is the deadliest type of skin cancer, arising from melanocytes, and its global incidence continues to rise. Although multiple somatic mutations contribute towards melanoma development, but the BRAF mutation is the most prevalent. The FDA approval of targeted therapies for BRAF-mutant melanoma greatly increased overall survival in considerable number of patients. However, the majority of patients eventually developed resistance against BRAF inhibitors (BRAFi) and the underlying mechanisms still under explorations. Recent research has revealed that long noncding RNAs (lncRNAs) are closely linked to the development and progression of several malignancies, including melanoma. However, the connection between lncRNA expression profiles and acquired resistance to melanoma BRAFi is in the early stages of research. Herein, we present a current summary of the ways by which lncRNAs either restore melanoma cell susceptibility to BRAFi or cause resistance. Additionally, we have also discussed the potential of lncRNAs role as prognostic indicators of response and resistance to BRAFi therapy in melanoma.
Insights
Long noncoding RNAs (lncRNAs) are emerging as key players in melanoma BRAF inhibitor (BRAFi) resistance. Understanding lncRNA roles can reveal new therapeutic strategies and prognostic markers for BRAFi-treated melanoma patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Melanoma, the deadliest skin cancer, is increasingly common globally.
- BRAF mutations are prevalent in melanoma, and targeted therapies (BRAFi) improve survival.
- Acquired resistance to BRAFi is a major clinical challenge, with underlying mechanisms under investigation.
Purpose of the Study:
- To summarize the current understanding of long noncoding RNAs (lncRNAs) in acquired resistance to BRAF inhibitors (BRAFi) in melanoma.
- To explore the dual role of lncRNAs in either restoring sensitivity or conferring resistance to BRAFi.
- To discuss the potential of lncRNAs as prognostic biomarkers for BRAFi therapy response and resistance.
Main Methods:
- Literature review and synthesis of recent research findings.
- Analysis of studies investigating lncRNA expression profiles in melanoma.
- Examination of functional studies on lncRNAs in the context of BRAFi treatment.
Main Results:
- lncRNAs are implicated in the development and progression of melanoma.
- Specific lncRNAs can either re-sensitize melanoma cells to BRAFi or promote resistance.
- lncRNA expression patterns correlate with treatment response and resistance.
Conclusions:
- lncRNAs represent a critical, yet underexplored, factor in BRAFi resistance in melanoma.
- Targeting lncRNAs may offer novel therapeutic avenues to overcome BRAFi resistance.
- lncRNAs hold promise as predictive biomarkers for patient stratification and treatment selection in melanoma.
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