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二甲基氨基米氏内酯使癌细胞对放疗敏感,以与免疫检查点阻断协同联合。

Dimethylaminomicheliolide Sensitizes Cancer Cells to Radiotherapy for Synergistic Combination with Immune Checkpoint Blockade.

作者信息

Li Yingying, Ni Kaiyuan, Chan Christina, Guo Nining, Luo Taokun, Han Wenbo, Culbert August, Weichselbaum Ralph R, Lin Wenbin

机构信息

Department of Chemistry University of Chicago Chicago, IL 60637, USA.

Department of Radiation and Cellular Oncology and The Ludwig Center for Metastasis Research University of Chicago, Chicago, IL 60637, USA.

出版信息

Adv Ther (Weinh). 2022 Jan;5(1). doi: 10.1002/adtp.202100160. Epub 2021 Oct 3.

Abstract

Radiotherapy (RT) has demonstrated synergy with immune checkpoint blockade (ICB) in preclinical models. However, its potential as an immunoadjuvant is limited by low immunogenicity at low radiation doses and immunosuppression at high radiation doses. It is hypothesized that radiosensitizers can enhance both the anticancer and immunogenic effects of low-dose radiation. Herein the authors report the antitumor immunity of combined RT and immunotherapy with dimethylaminomicheliolide (DMAMCL), a prodrug of the anti-inflammatory sesquiterpene lactone micheliolide (MCL). DMAMCL sensitized cancer cells to a single fraction of RT in vitro by inducing apoptosis and DNA double-strand breaks. DMAMCL with 5 fractions of 2 Gy focal X-ray irradiation led to significant anticancer efficacy in subcutaneous and spontaneous models of murine cancer. DMAMCL-sensitized RT upregulated programmed death-ligand 1 (PD-L1) expression in the tumors. Combination of DMAMCL-sensitized RT with anti-PD-L1 ICB significantly enhanced antitumor efficacy by increasing tumor-infiltrating CD4 and CD8 T cells and establishing immune memory.

摘要

放射疗法(RT)在临床前模型中已显示出与免疫检查点阻断(ICB)具有协同作用。然而,其作为免疫佐剂的潜力受到低辐射剂量下免疫原性低和高辐射剂量下免疫抑制的限制。据推测,放射增敏剂可以增强低剂量辐射的抗癌和免疫原性作用。在此,作者报告了联合RT与免疫疗法使用抗炎倍半萜内酯米氏内酯(MCL)的前药二甲基氨基米氏内酯(DMAMCL)的抗肿瘤免疫作用。DMAMCL在体外通过诱导细胞凋亡和DNA双链断裂使癌细胞对单次分割的RT敏感。DMAMCL与5次2 Gy局部X射线照射导致在小鼠癌症的皮下和自发模型中具有显著的抗癌疗效。DMAMCL增敏的RT上调了肿瘤中程序性死亡配体1(PD-L1)的表达。DMAMCL增敏的RT与抗PD-L1 ICB联合使用通过增加肿瘤浸润性CD4和CD8 T细胞并建立免疫记忆,显著增强了抗肿瘤疗效。

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