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肿瘤微环境中免疫抑制促进口腔恶性肿瘤的研究进展

Perspectives of Immune Suppression in the Tumor Microenvironment Promoting Oral Malignancy.

作者信息

Kondoh Nobuo, Mizuno-Kamiya Masako, Takayama Eiji, Kawati Harumi, Umemura Naoki, Yamazaki Yutaka, Mitsudo Kenji, Tohnai Iwai

机构信息

Department of Oral Biochemistry, Division of Oral Structure, Function and Development, Asahi University School of Dentistry, 1851 Hozumi, Mizuho, Gifu, 501-0296, Japan.

Department of Management and Information Studies, Chemistry Laboratory, Asahi University School of Business Administration, 1851 Hozumi, Mizuho, Gifu 501-0296, Japan.

出版信息

Open Dent J. 2018 Jun 20;12:455-465. doi: 10.2174/1874210601812010455. eCollection 2018.

DOI:10.2174/1874210601812010455
PMID:29988281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6018133/
Abstract

INTRODUCTION

In order to survive, cancers control immune systems and evade immune detection using mediators consisting of immune checkpoint molecules and cellular systems associated with immune suppression.

METHODOLOGY

During the development of cancer and chronic infections, the immune checkpoints and cellular components including regulatory T cells, myeloid derived suppressor cells and cancer associated fibroblasts are often enhanced as a mechanism of immune subversion and have therefore become very important therapeutic targets.

CONCLUSION

In this review, we will discuss the complexity of immune-suppressive mechanisms in the tumor milieu of cancers, including oral malignancy.

摘要

引言

为了生存,癌症利用由免疫检查点分子和与免疫抑制相关的细胞系统组成的介质来控制免疫系统并逃避免疫检测。

方法

在癌症和慢性感染的发展过程中,免疫检查点和细胞成分,包括调节性T细胞、髓源性抑制细胞和癌症相关成纤维细胞,常常会增强,作为一种免疫颠覆机制,因此已成为非常重要的治疗靶点。

结论

在本综述中,我们将讨论癌症肿瘤微环境中免疫抑制机制的复杂性,包括口腔恶性肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8f/6018133/38fa6d75f259/TODENTJ-12-455_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8f/6018133/38fa6d75f259/TODENTJ-12-455_F1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8f/6018133/38fa6d75f259/TODENTJ-12-455_F1.jpg

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2
Gene expression analyses associated with malignant phenotypes of metastatic sub-clones derived from a mouse oral squamous cell carcinoma Sq-1979 cell line.与源自小鼠口腔鳞状细胞癌Sq-1979细胞系的转移亚克隆恶性表型相关的基因表达分析。
Oncol Lett. 2018 Mar;15(3):3350-3356. doi: 10.3892/ol.2017.7648. Epub 2017 Dec 19.
3
Enrichment of Human CCR6 Regulatory T Cells with Superior Suppressive Activity in Oral Cancer.
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Cancers (Basel). 2022 Jun 11;14(12):2884. doi: 10.3390/cancers14122884.
4
The mechanisms of action of Plasmodium infection against cancer.疟原虫感染对抗癌症的作用机制。
Cell Commun Signal. 2021 Jul 9;19(1):74. doi: 10.1186/s12964-021-00748-5.
5
Immunomodulatory aspects in the progression and treatment of oral malignancy.口腔恶性肿瘤进展与治疗中的免疫调节方面
Jpn Dent Sci Rev. 2019 Nov;55(1):113-120. doi: 10.1016/j.jdsr.2019.09.001. Epub 2019 Oct 7.
口腔癌中具有卓越抑制活性的人CCR6调节性T细胞的富集
J Immunol. 2017 Jul 15;199(2):467-476. doi: 10.4049/jimmunol.1601815. Epub 2017 Jun 9.
4
Regulatory T cells as suppressors of anti-tumor immunity: Role of metabolism.调节性 T 细胞作为抗肿瘤免疫的抑制物:代谢的作用。
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