Claudin-18.2 as a therapeutic target in cancers: cumulative findings from basic research and clinical trials

被引:47
|
作者
Kyuno, Daisuke [1 ,2 ]
Takasawa, Akira [1 ]
Takasawa, Kumi [1 ]
Ono, Yusuke [1 ]
Aoyama, Tomoyuki [1 ]
Magara, Kazufumi [1 ]
Nakamori, Yuna [1 ]
Takemasa, Ichiro [2 ]
Osanai, Makoto [1 ]
机构
[1] Sapporo Med Univ, Dept Pathol, Sapporo, Hokkaido, Japan
[2] Sapporo Med Univ, Dept Surg Surg Oncol & Sci, Sapporo, Hokkaido, Japan
来源
TISSUE BARRIERS | 2022年 / 10卷 / 01期
关键词
Tight junction; claudin-18.2; cancer; zolbetuximab; GASTRIC-CANCER; BARRIER DYSFUNCTION; DOWN-REGULATION; EXPRESSION; ADENOCARCINOMA; GENE; ZOLBETUXIMAB; DEFICIENCY; ANTIBODY; TRANSITION;
D O I
10.1080/21688370.2021.1967080
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Claudins are major components of tight junctions that maintain cell polarity and intercellular adhesion. The dynamics of claudins in cancer cells have attracted attention as a therapeutic target. During carcinogenesis, claudin expression is generally downregulated; however, overexpression of claudin-18.2 has been observed in several types of cancers. Upregulated and mislocalized claudin-18.2 expression in cancer cells has been suggested as a therapeutic target. Research on claudin-18.2 has revealed its involvement in carcinogenesis. Clinical trials using zolbetuximab, a monoclonal antibody targeting claudin-18.2, for patients with advanced cancer yielded positive results with few high-grade adverse events; thus, it is expected to be a novel and effective therapeutic. Here, we review current insights into the role that claudin-18.2 plays in basic cancer research and clinical applications. A better understanding of these roles will facilitate the development of new treatment strategies for cancer patients with poor prognoses.
引用
收藏
页数:16
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