The Role of Regulatory T Cells in Cancer Treatment Resistance

被引:7
|
作者
Dabrowska, Anna [1 ]
Grubba, Magdalena [1 ]
Balihodzic, Amar [2 ,3 ]
Szot, Olga [1 ]
Sobocki, Bartosz Kamil [1 ]
Perdyan, Adrian [4 ,5 ]
机构
[1] Med Univ Gdansk, Student Sci Circle Oncol & Radiotherapy, PL-80210 Gdansk, Poland
[2] Med Univ Graz, Comprehens Canc Ctr Graz, Dept Internal Med, Div Oncol, A-8036 Graz, Austria
[3] BioTechMed Graz, A-8010 Graz, Austria
[4] Med Univ Gdansk, 3P Med Lab, PL-80210 Gdansk, Poland
[5] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
关键词
regulatory T cell; resistance mechanisms; immunotherapy; chemotherapy; radiotherapy; TGF-BETA; ACQUIRED-RESISTANCE; RADIOTHERAPY; HETEROGENEITY; ANGIOGENESIS; CHEMOTHERAPY; EXPRESSION; BLOCKADE;
D O I
10.3390/ijms241814114
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite tremendous progress in cancer treatment in recent years, treatment resistance is still a major challenge for a great number of patients. One of the main causes is regulatory T lymphocytes (Tregs), which suppress excessive inflammatory responses via the secretion of immunosuppressive cytokines and upregulate the immune checkpoints. Their abundance causes an immunosuppressive reprogramming of the tumor environment, which is ideal for tumor growth and drug inefficiency. Hence, regiments that can regain tumor immunogenicity are a promising strategy to overcome Tregs-mediated drug resistance. However, to develop effective therapeutic regimens, it is essential to understand the molecular mechanisms of Treg-mediated resistance. In this article, we gathered a comprehensive summary of the current knowledge on molecular mechanisms and the role of Tregs in cancer treatment resistance, including cancer immunotherapy, targeted therapy, chemotherapy, and radiotherapy.
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页数:20
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