Tannins in Phyllanthus emblica L. improves cisplatin efficacy in lung cancer cells by boosting endoplasmic reticulum stress to trigger immunogenic cell death

• Published in: Phytomedicine (Stuttgart) 2024-01, Vol.123, p.155219-155219, Article 155219
• Main Authors: Hu, Qian, Wang, Shukai, Cheng, Ruiyang, Liu, Yuqi, Chang, Zihao, Huang, Ya, Chen, Yinxin, Luo, Xiaowei, Zhou, Lipeng, Wang, Baojin, Gao, Ye, Chen, Hongjiao, Liu, Runping, Zhang, Lanzhen
• Format: Article
• Language: English
• Subjects: Animals; Cell Line, Tumor; Cisplatin - therapeutic use; Endoplasmic Reticulum Stress; Humans; Immunogenic Cell Death; Lung Neoplasms - drug therapy; Lung Neoplasms - pathology; Mice; Phyllanthus emblica; Tannins - pharmacology; Tumor Microenvironment
• ISSN: 0944-7113; 1618-095X
• DOI: 10.1016/j.phymed.2023.155219

Lung cancer is one of the deadliest cancers world-wide and immunotherapy has been considered as a promising therapeutic strategy. Previously, our study found that tannins in Phyllanthus emblica L. (PTF) could inhibit the growth of tumor by activating the immune response in liver cancer, and also exhibited a cytotoxicity on human lung cancer cells A549, H460, H1703 in vitro. To explore whether PTF inhibited the growth of lung cancer through its immune-regulating function and to clarify underlying mechanisms. The induction of immunogenic cell death (ICD) were characterized by calreticulin exposure, extracellular ATP secretion, and High Mobility Group Box 1(HMGB1) release both in vivo using LLC-derived xenograft tumor model and in vitro using both mouse LLC and human A549 cancer cells. PTF inhibited lung cancer cells growth and tumorigenesis in vivo/vitro and promoted anti-tumor immune responses. We further found that PTF could induce ICD, which then activated Type I interferon responses and CXCL9/10-mediated chemotaxis. Mechanistically, PTF induced the formation of intracellular protein aggregates and following activation of PERK/ATF4/CHOP-dependent endoplasmic reticulum stress-related ICD. Moreover, PTF improved the antitumor efficacy of cisplatin by inducing ICD both in vitro and in vivo. Finally, we screened out 5 components from PTF, including gallocatechin, gallic acid, methyl gallate, ethyl gallate and ellagic acid, which could induce ICD in vitro and might be considered as the potential antitumor pharmacodynamic substances. In conclusion, PTF inhibits the growth of lung cancer by triggering ICD and remodeling the tumor microenvironment, suggesting that PTF may have promising prospects as an adjacent immunotherapy for cancers.