Radiotherapy modulates autophagy to reshape the tumor immune microenvironment to enhance anti-tumor immunity in esophageal cancer

IF 9.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Reviews on cancer Pub Date : 2025-03-20 DOI:10.1016/j.bbcan.2025.189302
Suna Zhou, Haihua Yang
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Abstract

The combination of radiotherapy and immunotherapy exerts synergistic antitumor in a range of human cancers, and also in esophageal cancer. Radiotherapy-induced tumor immune microenvironment (TIME) reprogramming is an essential basis for the synergistic antitumor between radiotherapy and immunotherapy. Radiotherapy can induce autophagy in tumor cells and immune cells of TIME, and autophagy activation is involved in the modification of immunological characteristics of TIME. The TIME landscape of esophageal cancer, especially ESCC, can be affected by radiotherapy or autophagy regulation. In this review, we depicted that local radiotherapy-induced autophagy could promote the maturation, migration, infiltration, and function of immune cells by complicated mechanisms to make TIME from immune “cold” to “hot”, resulting in the synergistic antitumor of RT and IO. We argue that unraveling the relevance of radiotherapy-initiated autophagy to driving radiotherapy reprogramming TIME will open new ideas to explore new targets or more efficiently multimodal therapeutic interventions in ESCC.
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放疗通过调节肿瘤自噬重塑肿瘤免疫微环境,增强食管癌的抗肿瘤免疫能力
放射治疗和免疫治疗的联合治疗对多种人类癌症和食管癌具有协同抗肿瘤作用。放疗诱导肿瘤免疫微环境(TIME)重编程是放疗与免疫治疗协同抗肿瘤的重要基础。放疗可诱导肿瘤细胞和TIME免疫细胞自噬,自噬激活参与了TIME免疫特性的改变。食管癌,尤其是ESCC的TIME分布可受放疗或自噬调节的影响。在本文中,我们描述了局部放疗诱导的自噬可以通过复杂的机制促进免疫细胞的成熟、迁移、浸润和功能,使时间从免疫“冷”到“热”,从而产生RT和IO的协同抗肿瘤作用。我们认为,揭示放射治疗引发的自噬与驱动放射治疗重编程时间的相关性,将为探索ESCC的新靶点或更有效的多模式治疗干预开辟新的思路。
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来源期刊
Biochimica et biophysica acta. Reviews on cancer
Biochimica et biophysica acta. Reviews on cancer 医学-生化与分子生物学
CiteScore
17.20
自引率
0.00%
发文量
138
审稿时长
33 days
期刊介绍: Biochimica et Biophysica Acta (BBA) - Reviews on Cancer encompasses the entirety of cancer biology and biochemistry, emphasizing oncogenes and tumor suppressor genes, growth-related cell cycle control signaling, carcinogenesis mechanisms, cell transformation, immunologic control mechanisms, genetics of human (mammalian) cancer, control of cell proliferation, genetic and molecular control of organismic development, rational anti-tumor drug design. It publishes mini-reviews and full reviews.
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