EphA2 specific chimeric antigen receptor engineered T cells for the treatment of prostate cancer

Erythropoietin-producing hepatocyte receptor A2 (EphA2) is an attractive target for immunotherapy due to its high expression in a variety of solid tumors including prostate cancer. Among various types of immunotherapeutics, chimeric antigen receptor T (CAR-T) cell therapy has made promising progress in hematological and solid tumors. Here, we detected the expression of EphA2 in prostate cancer cells and developed a second-generation CAR targeting EphA2 with CD28 as a co-stimulatory receptor to explore its tumor suppressive potential for prostate cancer in vitro and in vivo. EphA2 was highly expressed on the surface of PC3 and DU145 cells. EphA2 CART cells effectively inhibited prostate cancer growth in an antigen-dependent manner in vitro and in vivo. In addition, tumor cells could stimulate the proliferation of CAR-T cells and the release of cytokine IFN-γ in vitro. These findings shed light on EphA2 as a potential target for prostate cancer, promising EphA2 specific CAR-T cells for the treatment of prostate cancer.

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Publication Details

Journal
Translational Oncology
Published
2024-09-09
DOI
https://doi.org/10.1016/j.tranon.2024.102111
Citations
5
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
1.41

Funders

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article

EphA2 specific chimeric antigen receptor engineered T cells for the treatment of prostate cancer

Shibao Li, Junnian Zheng, Hai‐Ting Wang, Meng Wang et al.
5 citations
Translational Oncology
CAR-T cell therapy research
1.41
article

EphA2 specific chimeric antigen receptor engineered T cells for the treatment of prostate cancer

Shibao Li, Junnian Zheng, Hai‐Ting Wang, Meng Wang, Miaomiao Zhang, Gang Wang, Ping Ma, Haoliang Zhang, Huizhong Li
article en
5 citations

Abstract

Erythropoietin-producing hepatocyte receptor A2 (EphA2) is an attractive target for immunotherapy due to its high expression in a variety of solid tumors including prostate cancer. Among various types of immunotherapeutics, chimeric antigen receptor T (CAR-T) cell therapy has made promising progress in hematological and solid tumors. Here, we detected the expression of EphA2 in prostate cancer cells and developed a second-generation CAR targeting EphA2 with CD28 as a co-stimulatory receptor to explore its tumor suppressive potential for prostate cancer in vitro and in vivo. EphA2 was highly expressed on the surface of PC3 and DU145 cells. EphA2 CART cells effectively inhibited prostate cancer growth in an antigen-dependent manner in vitro and in vivo. In addition, tumor cells could stimulate the proliferation of CAR-T cells and the release of cytokine IFN-γ in vitro. These findings shed light on EphA2 as a potential target for prostate cancer, promising EphA2 specific CAR-T cells for the treatment of prostate cancer.

Translational OncologyVol. 50
Jiangsu University (CN), Xuzhou Medical College (CN), Xuzhou Cancer Hospital (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Government of Jiangsu Province, Xuzhou Medical University, Xuzhou Science and Technology Bureau, National Key Research and Development Program of China Stem Cell and Translational Research
Good health and well-being
Openalex Percentile: Top 15%
CAR-T cell therapy research
1.41
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