Department of Medicine and Surgery, Section of General Pathology, University of Perugia, S. Andrea delle Fratte, Perugia 06156, Italy.
Department of Medicine and Surgery, Faculty of Dentistry, University of Perugia, S. Andrea delle Fratte, Perugia 06156, Italy.
Arch Oral Biol. 2025 Jan;169:106110. doi: 10.1016/j.archoralbio.2024.106110. Epub 2024 Oct 16.
The present study examined the in vitro effects on oral squamous cell carcinoma cells (HSC-3) of cannabidiol (CBD), the main chemical component of Cannabis, proposed as a novel adjuvant therapy in the treatment of cancers.
Cell viability (MTT assay), morphology (SEM), apoptosis and cell cycle (flow cytometry), and DNA damage (phospho-γ-H2AX immunofluorescence) were evaluated. Cytotoxicity was evaluated with concentrations between 100 µM and 1 µM, and two concentrations were selected for subsequent analysis: 25 µM, as toxic dose, and 6.25 µM, as non-toxic.
CBD caused a dose- and time-dependent reduction in viability of 64 %, 96 %, and 99 % with 25 µM, 50 µM and 100 µM, respectively, after 72 h (p < 0.001), cell cycle arrest in G0-G1 phase with increased apoptosis in particular at 72 h for 25 µM (p < 0.001), significant morphological alterations with 25 µM, still present even at 6.25 µM, and significantly increased cell damage considering a significant increase in the percentage of highly positive cells (5 phosphorylated γH2AX foci), which is around 29 % for 25 µM and 19 % for 6.25 µM after 24 h.
CBD inhibits oral cancer growth causing DNA damage. In general, induced cell cytotoxicity appears to be dose- and time-related. Doses of CBD ≥25 μM showed a high reduction in viability. CBD could possibly represent a new therapeutic molecule for its cytotoxic effects against oral squamous cell carcinoma. The mechanism involved in the suppressive effect caused by CBD needs further investigation.
本研究探讨了大麻的主要化学成分大麻二酚 (CBD) 对口腔鳞状细胞癌细胞 (HSC-3) 的体外作用,CBD 被提议作为癌症治疗的一种新辅助疗法。
评估细胞活力 (MTT 测定)、形态 (SEM)、细胞凋亡和细胞周期 (流式细胞术) 以及 DNA 损伤 (磷酸化 γ-H2AX 免疫荧光)。用浓度在 100µM 和 1µM 之间进行细胞毒性评估,并选择两个浓度进行后续分析:25µM,作为毒性剂量,6.25µM,作为非毒性剂量。
CBD 导致细胞活力以剂量和时间依赖的方式下降,25µM、50µM 和 100µM 分别在 72 小时后下降 64%、96%和 99%(p<0.001),细胞周期停滞在 G0-G1 期,特别是在 72 小时时凋亡增加(p<0.001),25µM 时形态发生显著改变,即使在 6.25µM 时仍存在,并且细胞损伤明显增加,考虑到高度阳性细胞(5 个磷酸化 γH2AX 焦点)的百分比显著增加,25µM 时约为 29%,6.25µM 时约为 19%,在 24 小时后。
CBD 抑制口腔癌生长并导致 DNA 损伤。一般来说,诱导的细胞细胞毒性似乎与剂量和时间有关。CBD 剂量≥25µM 显示出高的细胞活力降低。CBD 可能因其对口腔鳞状细胞癌的细胞毒性作用而成为一种新的治疗分子。CBD 引起的抑制作用的机制需要进一步研究。