Sen Prakriti, Sadat Sayed, Ebisumoto Koji, Al-Msari Riyam, Miyauchi Sayuri, Roy Souvick, Mohammadzadeh Pardis, Lips Kristin, Nakagawa Takuya, Saddawi-Konefka Robert, Sharabi Andrew B, Califano Joseph A
Gleiberman Head and Neck Cancer Center, Moores Cancer Center, University of California San Diego, La Jolla, CA, United States.
Department of Otolaryngology-Head and Neck Surgery, Moores Cancer Center, University of California San Diego Health, La Jolla, CA, United States.
Front Immunol. 2025 May 22;16:1528520. doi: 10.3389/fimmu.2025.1528520. eCollection 2025.
Marijuana use is associated with HPV-positive head and neck squamous cell carcinoma (HNSCC). However, cannabinoid use continues to increase in the US general population for recreational purposes as well as in cancer patients for palliative care. In this study, we explored the role of cannabidiol (CBD) in promoting anti-tumor activity by modulating immune response in HPV-positive HNSCC by using pre-clinical models.
The anti-proliferative effect of CBD on HPV-positive HNSCC cells was evaluated through BrdU, apoptosis and migration analyses, followed by western blot analysis to assess its role in activating the MAPK pathway. Next, the anti-tumor immune response of CBD was evaluated in immunocompetent syngeneic mouse as well as in immune-deficient B6.129S7-Rag1/J or Rag 1 Knockout mice (Rag1 -/-) and athymic nude mouse. Immune cell infiltration was measured by flow cytometry, IHC and multiplex IHC analysis after subcutaneous injection of mEER cells. Furthermore, the anti-tumor activity of CBD on the tumor microenvironment was evaluated after the depletion of CD4+T cells and CD8+T cells in murine models.
We observed CBD treatment inhibited cell proliferation and migration by promoting apoptosis in HPV-positive HNSCC cells through activation of the MAPK pathway and its associated markers like ERK1/2, JNK/SAPK and MK2. CBD significantly inhibited tumor growth in immunocompetent mice but had no effect in immune-deficient models, indicating an immune-dependent mechanism. CBD enhanced infiltration of CD4+T and CD8+T cells, CD19+B cells, NK cells, and M1-like macrophages into the primary tumors of immunocompetent syngeneic mice models, implicating an enhanced anti-tumor immune response. Interestingly, we observed a significant increase in tumor volume in CD4-depleted mice treated with CBD as compared to CBD-treated wild-type mice suggesting the importance of CD4+T cells in CBD-mediated anti-tumor activity. Finally, multiplex IHC analysis demonstrated co-localization of CD4+T and CD8+ T cells with the activated MAPK marker phospho-p38 in CBD-treated tumors.
CBD inhibits tumor cell proliferation in HPV-positive HNSCC by activating the MAPK pathway. It also enhances anti-tumor activity by modulating the tumor immune microenvironment, promoting co-localization of p38 MAPK-activated CD4+ and CD8+ T cells.
大麻使用与HPV阳性头颈部鳞状细胞癌(HNSCC)相关。然而,在美国普通人群中,出于娱乐目的使用大麻素的情况持续增加,在癌症患者中用于姑息治疗的情况也是如此。在本研究中,我们通过使用临床前模型,探讨了大麻二酚(CBD)在HPV阳性HNSCC中通过调节免疫反应来促进抗肿瘤活性的作用。
通过BrdU、凋亡和迁移分析评估CBD对HPV阳性HNSCC细胞的抗增殖作用,随后进行蛋白质印迹分析以评估其在激活MAPK途径中的作用。接下来,在具有免疫活性的同基因小鼠以及免疫缺陷的B6.129S7-Rag1/J或Rag 1基因敲除小鼠(Rag1 -/-)和无胸腺裸鼠中评估CBD的抗肿瘤免疫反应。皮下注射mEER细胞后,通过流式细胞术、免疫组化(IHC)和多重免疫组化分析测量免疫细胞浸润情况。此外,在小鼠模型中耗竭CD4+T细胞和CD8+T细胞后,评估CBD对肿瘤微环境的抗肿瘤活性。
我们观察到,CBD处理通过激活MAPK途径及其相关标志物如ERK1/2、JNK/SAPK和MK2,促进HPV阳性HNSCC细胞凋亡,从而抑制细胞增殖和迁移。CBD显著抑制具有免疫活性小鼠的肿瘤生长,但在免疫缺陷模型中无作用,表明其作用机制依赖于免疫。CBD增强了CD4+T细胞、CD8+T细胞、CD19+B细胞、NK细胞和M1样巨噬细胞向具有免疫活性的同基因小鼠模型原发性肿瘤中的浸润,这意味着抗肿瘤免疫反应增强。有趣的是,我们观察到,与用CBD处理的野生型小鼠相比,用CBD处理的CD4耗竭小鼠的肿瘤体积显著增加,这表明CD4+T细胞在CBD介导的抗肿瘤活性中具有重要作用。最后,多重免疫组化分析表明,在经CBD处理的肿瘤中,CD4+T细胞和CD8+T细胞与激活的MAPK标志物磷酸化p38共定位。
CBD通过激活MAPK途径抑制HPV阳性HNSCC中的肿瘤细胞增殖。它还通过调节肿瘤免疫微环境,促进p38 MAPK激活的CD4+和CD8+T细胞共定位,从而增强抗肿瘤活性。