Cytotoxic effects of cannabidiol on human metastatic melanoma cells: a potential therapeutic strategy?

Authors

  • Maria Moreira FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal
  • Natanael Videira FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal
  • Verónica Rocha FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal
  • José Catita FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal; Paralab, SA, 4420-392 Valbom, Portugal
  • Sérgio Barreira FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal; RISE HEALTH – UFP; Faculdade Ciências da Saúde, Universidade Fernando Pessoa, Porto, Portugal
  • Ana Margarida Araújo LAQV/REQUIMTE, Laboratory of Bromatology and Hydrology, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313, Porto, Portugal
  • Márcia Carvalho FFP-I3ID, FP-BHS, Faculty of Health Sciences, Fernando Pessoa University, 4200-150 Porto, Portugal; RISE HEALTH – UFP; Faculdade Ciências da Saúde, Universidade Fernando Pessoa, Porto, Portugal; LAQV/REQUIMTE, Laboratory of Bromatology and Hydrology, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313, Porto, Portugal

DOI:

https://doi.org/10.48797/sl.2025.380

Keywords:

Poster

Abstract

Background: Melanoma is the most aggressive form of skin cancer, responsible for the majority of skin cancer-related deaths due to its high metastatic potential and resistance to treatment [1]. The limited efficacy of systemic therapies in treating this disease underscores the need to explore novel therapeutic strategies. Cannabidiol (CBD), a bioactive compound from Cannabis sativa, has shown anticancer properties in various cancer models [2,3]. However, its effects on melanoma cells and its potential selectivity remain under investigation. Objective: This study evaluates the cytotoxic effects of CBD on human metastatic melanoma cells. Methods: Two melanoma cell lines (A375 and MeWo) and a normal human keratinocyte cell line (HaCaT) were treated with CBD (0.05-100 µM) for 24 and 48 hours. Cell viability was assessed by the MTT assay, and morphological changes were analyzed by inverted light microscopy. Results: CBD reduced cell viability in a concentration-dependent manner in all cell lines. HaCaT cells were the most sensitive with IC50 values at 24 h of 4.1 µM, followed by A375 (IC50 5.1 µM) and MeWo (IC50 5.8 µM) cells. Similar values were observed at 48 h (p > 0.05), indicating no significant time-dependent effect. Morphological changes were observed in all cell lines, becoming more pronounced with increasing CBD concentration and exposure time. Conclusions: CBD is a promising candidate for melanoma management. However, its non-selective cytotoxicity toward melanoma cells remains a major challenge for safe clinical application. Ongoing research aims to elucidate the molecular mechanisms underlying CBD-induced cytotoxicity and to explore strategies for improving selectivity, potentially enhancing its clinical applicability in melanoma treatment.

References

1. Fateeva, A. et al. Current state of melanoma therapy and next sSteps: Battling therapeutic resistance. Cancers 2024, 16, 1571, doi:10.3390/cancers16081571.

2. Faiz, M.B. et al. Exploring the therapeutic potential of cannabinoids in cancer by modulating signaling pathways and addressing clinical challenges. Discov Oncol 2024, 15, 490, doi:10.1007/s12672-024-01356-8.

3. Mashabela, M.D. et al. Anti-cancer and anti-proliferative potential of cannabidiol: A cellular and molecular perspective. Int J Mol Sci 2024, 25, 5659, doi:10.3390/ijms25115659.

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Published

2025-05-27

How to Cite

Moreira , M. ., Videira , N. ., Rocha , V., Catita , J. ., Barreira , S. ., Araújo , A. M., & Carvalho , M. . (2025). Cytotoxic effects of cannabidiol on human metastatic melanoma cells: a potential therapeutic strategy?. Scientific Letters, 1(Sup 1). https://doi.org/10.48797/sl.2025.380

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