Dataset Information

Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

ABSTRACT:

Background

Gastric cancer (GC) has a poor prognosis and limited therapeutic options. As a new promising cancer therapeutic approach, chimeric antigen receptor (CAR)-T cells represent a potential GC treatment. We investigated the antitumor activity of CAR-T cells target-B7H3 in GC.

Methods

In our study, expression of B7H3 was examined in GC tissues and explored the tumoricidal potential of B7H3-targeting CAR-T cells in GC. B7H3-directed CAR-T cells with a humanized antigen-recognizing domain was generated. The anti-tumor effects of this CAR-T cell were finally investigated in vitro and in vivo.

Results

Our results show that B7H3-directed CAR-T cells efficiently killed GC tumor cells. In addition, we found that B7H3 is correlated with tumor cell stemness, and anti-B7H3 CAR-T can simultaneously target stem cell-like GC cells to improve the treatment outcome.

Conclusions

Our study indicates that B7H3 is an attractive target for GC therapy, and B7H3 has high potential for clinical application.

SUBMITTER: Sun F

PROVIDER: S-EPMC8802437 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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Publications

Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

Sun Fengqiang F Yu Xiaomei X Ju Ruixue R Wang Zhanzhao Z Wang Yuhui Y

Cancer cell international 20220131 1

<h4>Background</h4>Gastric cancer (GC) has a poor prognosis and limited therapeutic options. As a new promising cancer therapeutic approach, chimeric antigen receptor (CAR)-T cells represent a potential GC treatment. We investigated the antitumor activity of CAR-T cells target-B7H3 in GC.<h4>Methods</h4>In our study, expression of B7H3 was examined in GC tissues and explored the tumoricidal potential of B7H3-targeting CAR-T cells in GC. B7H3-directed CAR-T cells with a humanized antigen-recogniz ...[more]

PMID: 35101032

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Dataset Information

Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

Background

Methods

Results

Conclusions

Publications

Antitumor responses in gastric cancer by targeting B7H3 via chimeric antigen receptor T cells.

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