Degan Simone, May Brian L, Jin Yingai J, Hammoda Manel Ben, Sun Huiying, Zhang Guoqiang, Wang Yan, Erdmann Detlev, Warren Warren, Zhang Jennifer Y
Department of Dermatology, Duke University Medical Center, Durham, NC, United States.
Department of Chemistry, Duke University, Durham, NC, United States.
Front Oncol. 2022 Jun 30;12:782877. doi: 10.3389/fonc.2022.782877. eCollection 2022.
Autophagy is characterized as a cytoprotective process and inhibition of autophagy with medicinally active agents, such as chloroquine (CQ) is proposed as a prospective adjuvant therapy for cancer. Here, we examined the preclinical effects of CQ combined with the MEK inhibitor trametinib (TRA) on melanoma. We found that cotreatment of CQ and TRA markedly slowed melanoma growth induced in . mice. Immunostaining showed that trametinib decreased Ki-67+ proliferating cells, and increased TUNEL+ apoptotic cells. The combo treatment induced a further decrease of Ki-67+ proliferating cells. Consistent with the findings, CQ and TRA inhibited melanoma cell proliferation , which was correlated by decreased cyclin D1 expression. In addition, we found that tissues treated with CQ and TRA had significantly decreased numbers of CD4+ and CD8+ T-lymphocytes and F4/80+ macrophages. Together, these results indicate that cotreatment of CQ and TRA decreases cancer cell proliferation, but also dampens immune cell infiltration. Further study is warranted to understand whether CQ-induced immune suppression inadvertently affects therapeutic benefits.
自噬被认为是一种细胞保护过程,使用具有药理活性的药物(如氯喹)抑制自噬被提议作为一种潜在的癌症辅助治疗方法。在此,我们研究了氯喹联合MEK抑制剂曲美替尼(TRA)对黑色素瘤的临床前效应。我们发现氯喹和曲美替尼联合治疗显著减缓了小鼠体内诱导的黑色素瘤生长。免疫染色显示曲美替尼减少了Ki-67+增殖细胞,并增加了TUNEL+凋亡细胞。联合治疗进一步降低了Ki-67+增殖细胞。与这些发现一致,氯喹和曲美替尼抑制了黑色素瘤细胞增殖,这与细胞周期蛋白D1表达降低相关。此外,我们发现用氯喹和曲美替尼处理的组织中CD4+和CD8+ T淋巴细胞以及F4/80+巨噬细胞的数量显著减少。总之,这些结果表明氯喹和曲美替尼联合治疗降低了癌细胞增殖,但也抑制了免疫细胞浸润。有必要进一步研究以了解氯喹诱导的免疫抑制是否会无意中影响治疗效果。