CD276
Protein found in humans
From Wikipedia, the free encyclopedia
Cluster of Differentiation 276 (CD276) or B7 Homolog 3 (B7-H3) is a human protein encoded by the CD276 gene.[5]
| CD276 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | CD276, 4Ig-B7-H3, B7-H3, B7H3, B7RP-2, CD276 molecule | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 605715; MGI: 2183926; HomoloGene: 11892; GeneCards: CD276; OMA:CD276 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Structure
B7-H3 is a 316 amino acid-long type I transmembrane protein, existing in two isoforms determined by its extracellular domain. In mice, the extracellular domain consists of a single pair of immunoglobulin variable (IgV)-like and immunoglobulin constant (IgC)-like domains, whereas in humans it consists of one pair (2Ig-B7-H3) or two identical pairs (4Ig-B7-H3) due to exon duplication. B7-H3 mRNA is expressed in most normal tissues. In contrast, B7-H3 protein has a very limited expression on normal tissues because of its post-transcriptional regulation by microRNAs. However, B7-H3 protein is expressed at high frequency on many different cancer types (60% of all cancers).[6] The 4Ig-B7-H3 isoform is predominant in cancer.[7]
Function
In non-malignant tissues, B7-H3 has a predominantly inhibitory role in adaptive immunity, suppressing T cell activation and proliferation.
In malignant tissues, B7-H3 is an immune checkpoint molecule that inhibits tumor antigen-specific immune responses. B7-H3 also possesses non-immunological pro-tumorigenic functions such as promoting migration, invasion, angiogenesis, chemoresistance, epithelial-to-mesenchymal transition, and affecting tumor cell metabolism.[6]
As a possible drug target
Due to its selective expression on solid tumors, B7-H3 has been the target of several anticancer agents such as enoblituzumab (MGA271),[8] omburtamab, MGD009, MGC018, DS-7300a, and CAR T cells.[6][7] Nanobodies targeting the IgV and IgC domains of B7-H3 have been developed in the laboratory of Mitchell Ho at the NCI, NIH (Bethesda, US). The nanobody-based CAR T cells are active in preclinical models of pancreatic cancer and neuroblastoma and show efficacy against large tumors in mice.[7]
