Affiliation:
1. Department of Tumor Biology, Institute for Cancer Research, Oslo University Hospital Radiumhospitalet, Oslo, Norway
Abstract
B7-H3 belongs to the B7 family of immune checkpoint proteins, which are important
regulators of the adaptive immune response and emerging key players in human cancer.
B7-H3 is a transmembrane protein expressed on the surface of tumor cells, antigen presenting
cells, natural killer cells, tumor endothelial cells, but can also be present in intra- and extracellular
vesicles. Additionally, B7-H3 may be present as a circulating soluble isoform in serum
and other body fluids. B7-H3 is overexpressed in a variety of tumor types, in correlation with
poor prognosis. B7-H3 is a promising new immunotherapy target for anti-cancer immune response,
as well as a potential biomarker. Besides its immunoregulatory role, B7-H3 has intrinsic
pro-tumorigenic activities related to enhanced cell proliferation, migration, invasion, angiogenesis,
metastatic capacity and anti-cancer drug resistance. B7-H3 has also been found to
regulate key metabolic enzymes, promoting the high glycolytic capacity of cancer cells. B7-H3
receptors are still not identified, and little is known about the molecular mechanisms underlying
B7-H3 functions. Here, we review the current knowledge on the involvement of B7-H3 in
human cancer.
Funder
The Research Council of Norway
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
Cited by
57 articles.
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