Calmette-Guerin芽孢杆菌通过下调ARID1A诱导CD8+ T细胞浸润,抑制微卫星稳定型结直肠癌肿瘤进展。

IF 5 3区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Zhiyue Xie, Nan Peng, Zhihua Pan, Yun Feng, Yihan Wu, Yansheng Yang, Rui Li, Liang Zhao
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引用次数: 0

摘要

新辅助免疫治疗对微卫星稳定型(MSS)结直肠癌(CRC)的疗效有限。在体内和体外条件下,卡介苗(Bacillus calmetate - gusamrin, BCG)均能抑制MSS-CRC的进展并下调ARID1A。通过对临床样本、体内体外模型和生物信息学的分析,我们发现ARID1A的低表达在体外促进肿瘤生长;然而,在体内,它可以增强MSS-CRC组织中CD8+ T细胞的浸润,同时抑制肿瘤的生长。进一步研究发现,BCG通过TLR4/NF-κB通路下调ARID1A,导致MSS-CRC中MLH1和PMS2的下调以及随后MMR功能的改变。这种级联反应增强抗原呈递,促进CD8+ T细胞浸润,有助于抑制肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bacillus Calmette-Guerin induces CD8+ T cell infiltration and suppresses tumor progression in microsatellite stable colorectal cancer by downregulating ARID1A.

Neoadjuvant immunotherapy demonstrates limited efficacy in microsatellite-stable (MSS) colorectal cancer (CRC). In vivo observations reveal that Bacillus Calmette-Guérin (BCG) can inhibit the progression of MSS-CRC and downregulate ARID1A in both in vivo and in vitro settings. Through the analysis of clinical samples, in vivo and in vitro models, and bioinformatics, we found that the low expression of ARID1A promotes tumor growth in vitro; however, in vivo, it enhances CD8+ T cell infiltration in MSS-CRC tissues while inhibiting tumor growth. Further investigation revealed that BCG downregulates ARID1A via the TLR4/NF-κB pathway, leading to the downregulation of MLH1 and PMS2 and subsequent alterations in MMR function in MSS-CRC. This cascade enhances antigen presentation, promotes CD8+ T cell infiltration, and contributes to tumor suppression.

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来源期刊
Cancer gene therapy
Cancer gene therapy 医学-生物工程与应用微生物
CiteScore
10.20
自引率
0.00%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Cancer Gene Therapy is the essential gene and cellular therapy resource for cancer researchers and clinicians, keeping readers up to date with the latest developments in gene and cellular therapies for cancer. The journal publishes original laboratory and clinical research papers, case reports and review articles. Publication topics include RNAi approaches, drug resistance, hematopoietic progenitor cell gene transfer, cancer stem cells, cellular therapies, homologous recombination, ribozyme technology, antisense technology, tumor immunotherapy and tumor suppressors, translational research, cancer therapy, gene delivery systems (viral and non-viral), anti-gene therapy (antisense, siRNA & ribozymes), apoptosis; mechanisms and therapies, vaccine development, immunology and immunotherapy, DNA synthesis and repair. Cancer Gene Therapy publishes the results of laboratory investigations, preclinical studies, and clinical trials in the field of gene transfer/gene therapy and cellular therapies as applied to cancer research. Types of articles published include original research articles; case reports; brief communications; review articles in the main fields of drug resistance/sensitivity, gene therapy, cellular therapy, tumor suppressor and anti-oncogene therapy, cytokine/tumor immunotherapy, etc.; industry perspectives; and letters to the editor.
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