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程序性死亡蛋白1(PD-1)抑制剂通过重新激活T细胞和诱导食管鳞状细胞癌G2/M期阻滞增强放射敏感性。

PD-1 Inhibitor Enhanced Radiosensitivity by Reactivating T Cells and Inducing G2/M Phase Arrest in Esophageal Squamous Cell Carcinoma.

作者信息

Hao Shengnan, Zhang Xiangyan, Han Litao, Ma Xiangli, Nie Yongzhan, Deng Jiaying, Zhu Hongcheng, Liu Qi, Ai Dashan, Chen Yun, Kong Zhaolu, Zhao Kuaile

机构信息

Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai 200032, China.

Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.

出版信息

Radiat Res. 2022 Nov 1;198(5):458-466. doi: 10.1667/RADE-22-00061.1.

Abstract

Radiotherapy is a main treatment for esophageal squamous cell carcinoma (ESCC), but radioresistance leads to treatment failure ultimately. The combination of radiotherapy and PD-1 inhibitors showed significant antitumor effects. Our study showed that high-immune score, IFNG and CD8A level were associated with a low-radiosensitivity index (RSI) in the TCGA-ESCC cohort. And blocking PD-1 promoted exhausted T cells proliferation and IFN-γ expression. PD-1 inhibitor-reactivated T cells promoted G2/M-phase arrest, apoptosis and impaired DNA damage in radioresistant cells in an IFN-γ-dependent manner. Our study showed PD-1 inhibitors promote radiosensitivity though enhancing exhausted T cells expansion and IFN-γ expression, and highlights that neoadjuvant anti-PD-1 therapy and radiotherapy could offer an optimum strategy for improving cancer patients' outcome.

摘要

放射疗法是食管鳞状细胞癌(ESCC)的主要治疗方法,但放射抗性最终会导致治疗失败。放射疗法与PD-1抑制剂联合使用显示出显著的抗肿瘤效果。我们的研究表明,在TCGA-ESCC队列中,高免疫评分、IFNG和CD8A水平与低放射敏感性指数(RSI)相关。阻断PD-1可促进耗竭T细胞增殖和IFN-γ表达。PD-1抑制剂重新激活的T细胞以IFN-γ依赖的方式促进放射抗性细胞中的G2/M期阻滞、凋亡并损害DNA损伤。我们的研究表明,PD-1抑制剂通过增强耗竭T细胞的扩增和IFN-γ表达来促进放射敏感性,并强调新辅助抗PD-1治疗和放射疗法可为改善癌症患者的预后提供最佳策略。

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