Chemokine-Directed Tumor Microenvironment Modulation in Cancer Immunotherapy

被引:145
作者
Bule, Pedro [1 ]
Aguiar, Sandra Isabel [1 ]
Aires-Da-Silva, Frederico [1 ]
Dias, Joana Nunes Ribeiro [1 ]
机构
[1] Univ Lisbon, Fac Med Vet, Ctr Invest Interdisciplinar Sanidade Anim, P-1300477 Lisbon, Portugal
关键词
cancer; chemokine; chemokine receptor; immunotherapy; tumoral microenvironment; REGULATORY T-CELLS; MYELOID SUPPRESSOR-CELLS; HUMAN MONOCLONAL-ANTIBODY; NON-HODGKIN-LYMPHOMA; CARLUMAB CNTO 888; CC-CHEMOKINE; CXCR4; ANTAGONIST; LIGAND; INDUCED SENESCENCE; PANCREATIC-CANCER;
D O I
10.3390/ijms22189804
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
Chemokines are a large family of small chemotactic cytokines that coordinates immune cell trafficking. In cancer, they have a pivotal role in the migration pattern of immune cells into the tumor, thereby shaping the tumor microenvironment immune profile, often towards a pro-tumorigenic state. Furthermore, chemokines can directly target non-immune cells in the tumor microenvironment, including cancer, stromal and vascular endothelial cells. As such, chemokines participate in several cancer development processes such as angiogenesis, metastasis, cancer cell proliferation, stemness and invasiveness, and are therefore key determinants of disease progression, with a strong influence in patient prognosis and response to therapy. Due to their multifaceted role in the tumor immune response and tumor biology, the chemokine network has emerged as a potential immunotherapy target. Under the present review, we provide a general overview of chemokine effects on several tumoral processes, as well as a description of the currently available chemokine-directed therapies, highlighting their potential both as monotherapy or in combination with standard chemotherapy or other immunotherapies. Finally, we discuss the most critical challenges and prospects of developing targeted chemokines as therapeutic options.
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页数:25
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