Centipeda minima and 6-O-angeloylplenolin enhance the efficacy of immune checkpoint inhibitors in non-small cell lung cancer

被引:1
|
作者
Wang, Min [1 ,2 ,3 ]
Guo, Hua [1 ]
Sun, Bei-Bei [1 ]
Jie, Xiao-Liang [1 ]
Shi, Xue-Yan [1 ]
Liu, Yong-Qiang [4 ]
Shi, Xu-Liu [5 ]
Ding, Li-Qin [5 ]
Xue, Peng-Hui [5 ]
Qiu, Feng [5 ]
Cao, Wei [6 ]
Wang, Gui-Zhen [1 ]
Zhou, Guang-Biao [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Natl Canc Ctr, Natl Clin Res Ctr Canc, State Key Lab Mol Oncol,Canc Hosp, Beijing 100021, Peoples R China
[2] Zhengzhou Univ, Affiliated Canc Hosp, Zhengzhou 450008, Peoples R China
[3] Henan Acad Innovat Med Sci, Henan Canc Hosp, Inst Canc Res, Zhengzhou 450008, Peoples R China
[4] Guangzhou Univ Chinese Med, Res Ctr Chinese Herbal Resources Sci & Engn, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R China
[5] Tianjin Univ Tradit Chinese Med, Sch Chinese Mat Med, Tianjin 301617, Peoples R China
[6] China Acad Chinese Med Sci, Wangjing Hosp, Beijing 100102, Peoples R China
基金
中国国家自然科学基金;
关键词
Non -small cell lung cancer; Immune checkpoint inhibitor; Centipeda minima; O; -angeloylplenolin; PD-L1; GSK-3; beta; beta-TRCP pathway; THERAPEUTIC-EFFICACY; NEGATIVE REGULATION; B7; FAMILY; PD-L1; PROLIFERATION; IMMUNOTHERAPY; EXPRESSION; MEMBER; SKP1;
D O I
10.1016/j.phymed.2024.155825
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Background: Chemotherapeutic agents including cisplatin, gemcitabine, and pemetrexed, significantly enhance the efficacy of immune checkpoint inhibitors (ICIs) in non-small cell lung cancer (NSCLC) by increasing PD-L1 expression and potentiating T cell cytotoxicity. However, the low response rate and adverse effects limit the application of chemotherapy/ICI combinations in patients. Methods: We screened for medicinal herbs that could perturb PD-L1 expression and enhance T cell cytotoxicity in the presence of anti-PD-L1 antibody, and investigated the underlying mechanisms. Results: We found that the aqueous extracts of Centipeda minima (CM) significantly enhanced the cancer cellkilling activity and granzyme B expression level of CD8+ T cells, in the presence of anti-PD-L1 antibody. Both CM and its active component 6-O-angeloylplenolin (6-OAP) upregulated PD-L1 expression by suppressing GSK3 beta-beta-TRCP-mediated ubiquitination and degradation. CM and 6-OAP significantly enhanced ICI-induced reduction of tumor burden and prolongation of overall survival of mice bearing NSCLC cells, accompanied by upregulation of PD-L1 and increase of CD8+ T cell infiltration. CM also exhibited anti-NSCLC activity in cells and in a patient-derived xenograft mouse model. Conclusions: These data demonstrated that the induced expression of PD-L1 and enhancement of CD8+ T cell cytotoxicity underlay the beneficial effects of 6-OAP-rich CM in NSCLCs, providing a clinically available and safe medicinal herb for combined use with ICIs to treat this deadly disease.
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页数:13
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