Harnessing B7-H6 for Anticancer Immunotherapy: Expression, Pathways, and Therapeutic Strategies

被引:0
|
作者
Lee, Sunyoung [1 ,2 ]
Kim, Ji Hyun [1 ,3 ]
Jang, In-Hwan [1 ]
Jo, Seona [1 ,3 ]
Lee, Soo Yun [1 ]
Oh, Se-Chan [1 ]
Kim, Seok-Min [1 ]
Kong, Lingzu [1 ,4 ]
Ko, Jesang [2 ]
Kim, Tae-Don [1 ,3 ]
机构
[1] Korea Res Inst Biosci & Biotechnol KRIBB, Ctr Cell & Gene Therapy, Daejeon 34141, South Korea
[2] Korea Univ, Div Life Sci, Seoul 02841, South Korea
[3] Korea Univ Sci & Technol UST, KRIBB Sch Biosci, Daejeon 34141, South Korea
[4] Chungnam Natl Univ, Coll Nat Sci, Dept Biochem, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
B7-H6; NKp30; cancer-specific target; targeted therapy; CHIMERIC ANTIGEN RECEPTORS; NATURAL CYTOTOXICITY RECEPTORS; PHOSPHOLIPASE C-GAMMA; FAMILY-MEMBER B7-H6; TUMOR-CELL LIGAND; ACTIVATING RECEPTOR; PROGNOSTIC VALUE; HEPARAN-SULFATE; NKP30; CANCER;
D O I
10.3390/ijms251910326
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
Cancer therapies have evolved from traditional chemotherapy to more precise molecular-targeted immunotherapies, which have been associated with improved side effects and outcomes. These modern strategies rely on cancer-specific biomarkers that differentiate malignant from normal cells. The B7 family of immune checkpoint molecules is crucial for cancer immune evasion and a prime therapeutic target. B7-H6, a recently identified member of the B7 family, has emerged as a promising therapeutic target. Unlike other B7 proteins, B7-H6 is not expressed in healthy tissues but is upregulated in several cancers. It binds to NKp30, activating natural killer (NK) cells and triggering immune responses against cancer cells. This review explores the expression of B7-H6 in different cancers, the factors that regulate its expression, and its intrinsic and extrinsic pathways. Additionally, we discuss potential anticancer therapies targeting B7-H6, highlighting its significance in advancing precision medicine. Understanding the role of B7-H6 in cancer immunity may inform the development of appropriate therapies that exploit its cancer-specific expression.
引用
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页数:16
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