Cell Trafficking at the Intersection of the Tumor-Immune Compartments

被引:8
|
作者
Du, Wenxuan [1 ,2 ]
Nair, Praful [1 ,2 ]
Johnston, Adrian [1 ,2 ]
Wu, Pei-Hsun [1 ,2 ]
Wirtz, Denis [1 ,2 ,3 ,4 ]
机构
[1] Johns Hopkins Univ, Inst NanoBiotechnol, Dept Chem & Biomol Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Johns Hopkins Phys Sci Oncol Ctr, Baltimore, MD 21218 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Dept Pathol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21205 USA
关键词
random migration; chemotaxis; immunotherapy; tumor microenvironment; EPITHELIAL-MESENCHYMAL TRANSITION; BOYDEN CHAMBER ASSAY; T-CELLS; TRANSENDOTHELIAL MIGRATION; CANCER-CELLS; EXTRACELLULAR VESICLES; NEUTROPHIL RECRUITMENT; PEGINTERFERON ALPHA-2A; SIGNALING PATHWAYS; PROGNOSTIC-FACTOR;
D O I
10.1146/annurev-bioeng-110320-110749
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Migration is an essential cellular process that regulates human organ development and homeostasis as well as disease initiation and progression. In cancer, immune and tumor cell migration is strongly associated with immune cell infiltration, immune escape, and tumor cell metastasis, which ultimately account for more than 90% of cancer deaths. The biophysics and molecular regulation of the migration of cancer and immune cells have been extensively studied separately. However, accumulating evidence indicates that, in the tumor microenvironment, the modifies of immune and cancer cells are highly interdependent via secreted factors such as cytokines and chemokines. Tumor and immune cells constantly express these soluble factors, which produce a tightly intertwined regulatory network for these cells' respective migration. A mechanistic understanding of the reciprocal regulation of soluble factor-mediated cell migration can provide critical information for the development of new biomarkers of tumor progression and of tumor response to immuno-oncological treatments. We review the biophysical and biomolecular basis for the migration of immune and tumor cells and their associated reciprocal regulatory network. We also describe ongoing attempts to translate this knowledge into the clinic.
引用
收藏
页码:275 / 305
页数:31
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