Preclinical CBD findings in cisplatin-resistant head and neck cancer

Cannabidiol impairs tumor-associated behaviors and modulates apoptosis- and autophagy-related pathways in cisplatin-resistant head and neck squamous cell carcinoma.

Medical oncology (Northwood, London, England) • • Highly Relevant
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AI Summary

This study asked whether cannabidiol (CBD) affects tumor-related behaviors in cisplatin-resistant, HPV-negative head and neck squamous cell carcinoma. Researchers tested HN13 cancer cells in laboratory assays, compared their response with fibroblasts and keratinocytes, and also used tumor spheroids and a chick chorioallantoic membrane model. The abstract reports no sample sizes or quantitative effect estimates.

CBD showed selective cytotoxicity toward HN13 cells and reduced migration, invasion, matrix metalloproteinase activity, clonogenic survival, and spheroid growth. In the membrane model, it reduced tumor growth and vascular area without causing vascular irritation. CBD also changed proteins linked to apoptosis, autophagy, and cell-cycle regulation; combining CBD with cisplatin produced synergistic cytotoxic effects in HN13 cells. These are preclinical findings, not evidence of benefit in people. The abstract-based summary cannot establish clinical effectiveness or safety, and the results require further preclinical investigation.

💡 Key Findings

1
In laboratory assays, CBD showed selective cytotoxicity toward cisplatin-resistant HN13 cancer cells compared with fibroblasts and keratinocytes.
High
80%
2
CBD reduced HN13-cell migration, invasion, metalloproteinase activity, clonogenic survival, and growth of 3D spheroids.
High
80%
3
In a chick membrane tumor model, CBD reduced tumor growth and vascular area without inducing vascular irritation.
Good
70%
4
CBD and cisplatin had synergistic cytotoxic effects in HN13 cells; the abstract reports no human treatment outcomes.
High
80%

📄 Original Abstract

Head and neck squamous cell carcinoma (HNSCC) remains a challenge due to recurrence, metastasis, and resistance to conventional therapies, particularly in human papillomavirus (HPV)-negative tumors. Cannabidiol (CBD), a non-psychoactive phytocannabinoid, has demonstrated antitumor activity in several cancer models; however, its effects in chemoresistant HNSCC are not well established. This study evaluates the antitumor effects of CBD and cellular mechanisms in a cisplatin -resistant, HPV-negative HNSCC model. Cytotoxic effects of CBD were assessed in HN13 cells and compared with fibroblasts and keratinocytes using MTT and selectivity index analysis. Migration, invasion, metalloproteinase activity, clonogenic survival, and cytotoxicity on 3D spheroids were evaluated. Cell death-related mechanisms were investigated using acridine orange/propidium iodide staining and Western blot analysis of apoptosis, autophagy, and cell-cycle regulation. Antitumor activity and vascular safety were further assessed using the chorioallantoic membrane model and HET-CAM assay. The combined effect of CBD and CIS was evaluated using the combination index analysis. CBD exhibited selective cytotoxicity toward HN13 cells and reduced migration, invasion, matrix metalloproteinase-2/9 activity, clonogenic survival, and 3D spheroid growth. CBD altered proteins associated with apoptosis, autophagy, and cell-cycle regulation. Pharmacological inhibition with 3-MA enhanced CBD-associated apoptotic signaling, increasing PARP and caspase-3 cleavage. In the CAM, CBD reduced tumor growth and vascular area without inducing vascular irritation. Furthermore, CBD and CIS demonstrated synergistic cytotoxic effects in HN13 cells. CBD exerted selective antitumor effects on CIS-resistant HN13 HNSCC cells, affecting tumor-associated behaviors and modulating apoptosis and autophagy-related signaling, while acting synergistically with cisplatin. These findings support further preclinical investigation of CBD as a potential adjunct approach in HNSCC, particularly in chemoresistant settings.

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