The Role of Regulatory T Cells in Cancer Treatment Resistance

Author:

Dąbrowska Anna1ORCID,Grubba Magdalena1,Balihodzic Amar23ORCID,Szot Olga1,Sobocki Bartosz Kamil1ORCID,Perdyan Adrian45ORCID

Affiliation:

1. Student Scientific Circle of Oncology and Radiotherapy, Medical University of Gdansk, 80-210 Gdansk, Poland

2. Division of Oncology, Department of Internal Medicine, Comprehensive Cancer Center Graz, Medical University of Graz, 8036 Graz, Austria

3. BioTechMed-Graz, 8010 Graz, Austria

4. 3P-Medicine Laboratory, Medical University of Gdansk, 80-210 Gdansk, Poland

5. Department of Biology, Stanford University, Stanford, CA 94305, USA

Abstract

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.

Funder

Foundation for Polish Science

NAWA-Polish National Agency for Academic Exchange

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference76 articles.

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