Cannabidiol Inhibits Tumorigenesis in Cisplatin-Resistant Non-Small Cell Lung Cancer via TRPV2.
Swati MisriKirti KaulSanjay MishraManish CharanAjeet Kumar VermaMartin P BarrDinesh K AhirwarRamesh K GanjuPublished in: Cancers (2022)
Chemotherapy forms the backbone of current treatments for many patients with advanced non-small-cell lung cancer (NSCLC). However, the survival rate is low in these patients due to the development of drug resistance, including cisplatin resistance. In this study, we developed a novel strategy to combat the growth of cisplatin-resistant (CR) NSCLC cells. We have shown that treatment with the plant-derived, non-psychotropic small molecular weight molecule, cannabidiol (CBD), significantly induced apoptosis of CR NSCLC cells. In addition, CBD treatment significantly reduced tumor progression and metastasis in a mouse xenograft model and suppressed cancer stem cell properties. Further mechanistic studies demonstrated the ability of CBD to inhibit the growth of CR cell lines by reducing NRF-2 and enhancing the generation of reactive oxygen species (ROS). Moreover, we show that CBD acts through Transient Receptor Potential Vanilloid-2 (TRPV2) to induce apoptosis, where TRPV2 is expressed on human lung adenocarcinoma tumors. High expression of TRPV2 correlates with better overall survival of lung cancer patients. Our findings identify CBD as a novel therapeutic agent targeting TRPV2 to inhibit the growth and metastasis of this aggressive cisplatin-resistant phenotype in NSCLC.
Keyphrases
- induced apoptosis
- advanced non small cell lung cancer
- endoplasmic reticulum stress
- oxidative stress
- small cell lung cancer
- cell cycle arrest
- signaling pathway
- epidermal growth factor receptor
- reactive oxygen species
- neuropathic pain
- cell death
- poor prognosis
- end stage renal disease
- endothelial cells
- newly diagnosed
- cancer stem cells
- dna damage
- chronic kidney disease
- squamous cell carcinoma
- prognostic factors
- ejection fraction
- spinal cord
- spinal cord injury
- drug delivery
- patient reported outcomes
- induced pluripotent stem cells
- blood brain barrier
- free survival
- risk assessment