Ren Yulin, Gallucci Judith C, Yu Jianhua, Burdette Joanna E, Fuchs James R, Kinghorn A Douglas
Division of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, The Ohio State University, Columbus, OH 43210, United States.
Division of Hematology & Oncology, Department of Medicine, School of Medicine, University of California Irvine, Irvine, CA 92697, United States; The Clemons Family Center for Transformative Cancer Research, Chao Family Comprehensive Cancer Center, University of California Irvine, Irvine, CA 92697, United States.
Bioorg Med Chem. 2025 Jul 1;124:118197. doi: 10.1016/j.bmc.2025.118197. Epub 2025 Apr 14.
Immune surveillance plays a key role in controlling tumor formation and development, and immune cell-based therapies, such as chimeric antigen receptor (CAR)-T cells and CAR-natural killer (NK) cells, have become important for the treatment of cancer. The proton pump (PP), vacuolar H-ATPase (V-ATPase), acidifies intracellular organelles, pumps protons across the cell plasma membranes, and regulates the activity of various signaling pathways, and thus has been regarded as a potential target for cancer treatment. In addition, V-ATPase plays an important role in cytotoxic T lymphocytes, extracellular vesicle (EV) endocytosis, innate immune responses (IIR), and phagocytosis and hence has the potential to function as a target for the enhancement of immunotherapy. As potent V-ATPase inhibitors, the arylnaphthalene lignans, diphyllin and its derivatives, have exhibited potent antitumor and immunomodulatory activities. The structurally related aryltetralin lignan, podophyllotoxin, has served as a lead compound for both etoposide and teniposide, which have been developed as effective anticancer agents. In the present review, the role of V-ATPase in cancer immunotherapy and the structure-activity relationships (SARs) of diphyllin and its cytotoxic and V-ATPase inhibitory activities and the mechanisms of action are discussed. Also, the promise of diphyllin and its derivatives in the development of new adjuvants for cancer immunotherapies has been proposed.
免疫监视在控制肿瘤形成和发展中起关键作用,基于免疫细胞的疗法,如嵌合抗原受体(CAR)-T细胞和CAR-自然杀伤(NK)细胞,已成为癌症治疗的重要手段。质子泵(PP),即液泡H-ATP酶(V-ATPase),可酸化细胞内细胞器,将质子泵过细胞质膜,并调节各种信号通路的活性,因此被视为癌症治疗的潜在靶点。此外,V-ATPase在细胞毒性T淋巴细胞、细胞外囊泡(EV)内吞作用、先天免疫反应(IIR)和吞噬作用中起重要作用,因此有潜力作为增强免疫治疗的靶点。作为有效的V-ATPase抑制剂,芳基萘木脂素、双叶豆素及其衍生物已表现出强大的抗肿瘤和免疫调节活性。结构相关的芳基四氢萘木脂素鬼臼毒素已作为依托泊苷和替尼泊苷的先导化合物,这两种药物已被开发为有效的抗癌药物。在本综述中,讨论了V-ATPase在癌症免疫治疗中的作用以及双叶豆素及其细胞毒性和V-ATPase抑制活性的构效关系(SARs)和作用机制。此外,还提出了双叶豆素及其衍生物在开发新型癌症免疫治疗佐剂方面的前景。