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January 1, 2020International Journal of Biological Sciences250 citationsOpen Access

B7-H3, a checkpoint molecule, as a target for cancer immunotherapy

SYShuo YangWWWei WeiQZQi Zhao

Key Points

  • To provide a comprehensive and up-to-date summary of B7-H3 (CD276) targeting approaches and evaluate its potential as a target for cancer immunotherapy.
  • Narrative review summarizing current evidence on B7-H3 expression in tumors, immunological mechanisms, and targeted therapeutic development.
  • B7-H3 (CD276) is expressed across multiple tumor types, including non-small-cell lung cancer and prostate cancer, and is strongly associated with poor prognosis and reduced survival.
  • B7-H3 functions both as a regulator of T-cell activation and in nonimmunological tumor signaling pathways, offering a target for cancer therapies with enhanced efficacy and lower toxicity.

Abstract

B7-H3 (also known as CD276) is a newly found molecule of B7 family, which may be a promising target for cancer treatment. B7-H3 protein was demonstrated to be expressed in several kinds of tumor tissues including non-small-cell lung cancer (NSCLC) and prostate cancer. Its expression is highly associated with undesirable treatment outcomes and survival time, due to function of the immune checkpoint molecule. It was classified as either a co-stimulatory molecule for T cell activation or the nonimmunological role of regulating signaling pathways. Although there is still no agreed conclusion on the function of B7-H3, it may be a valuable target for cancer therapy. This review aims to provide a comprehensive, up-to-date summary of the advances in B7-H3 targeting approaches in cancer therapy. Although several challenges remain, B7-H3 offers a new therapeutic target with increased efficacy and less toxicity in future cancer treatment.

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Cite This Study

Yang et al. (2020) studied this question.

synapsesocial.com/papers/699ffdb1bae4b1758c863a94https://doi.org/10.7150/ijbs.41105
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