间皮瘤
癌症研究
钙网蛋白
永生化细胞系
程序性细胞死亡
免疫原性细胞死亡
遗传增强
细胞凋亡
肿瘤微环境
生物
免疫学
内质网
细胞培养
免疫系统
免疫疗法
医学
细胞生物学
基因
病理
生物化学
遗传学
作者
Kenji Araki,Naoya Yamamuro,Nahoko Tomonobu,Hiromi Kumon
出处
期刊:Anticancer Research
[Anticancer Research USA Inc.]
日期:2021-10-01
卷期号:41 (10): 4837-4855
被引量:4
标识
DOI:10.21873/anticanres.15298
摘要
Background/Aim: The adenovirus vector– carrying reduced expression in immortalized cell (REIC) gene (Ad-REIC) increases endoplasmic reticulum stress chaperone GRP78/BiP expression and induces the JNK-mediated apoptotic pathway. We aimed to determine whether Ad-REIC–induced apoptotic cell death can trigger immunogenic cell death (ICD). Materials and Methods: We examined the emission of damage-associated molecular patterns in vitro and the vaccination effect in vivo. We determined the immunological changes in the tumour microenvironment by putative ICD inducers and the combined effects of immune checkpoint blockade therapies. Results: Ad-REIC induced the release of high-mobility group box 1 and adenosine triphosphate and the translocation of calreticulin in murine mesothelioma AB12 cells. The vaccination effect was elicited by Ad-REIC treatment in vivo. The effect of Ad-REIC was potentiated by anti-cytotoxic T-lymphocyte–associated protein 4 antibody treatment in a murine mesothelioma AB1-HA cell model. Conclusion: Ad-REIC induces ICD in malignant mesothelioma.
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