Abstract 4771: A novel immunotherapy for metastatic prostate cancer: A monoclonal antibody that can bind both STEAP1 and STEAP2

Prostate cancer (PCa) is the most common cancer among Canadian men, with metastatic PCa (mPCa) patients having a 5-year survival rate of only 30%. However, the prostate-specific membrane antigen, a key target in PCa therapy, is expressed in many normal tissues and shows heterogeneity among PCa patients. Recently, Six Transmembrane Epithelial Antigens of the Prostate 1 and 2 (STEAP1 and STEAP2) have gained attention as promising therapeutic targets due to their high expression in most PCa cases compared to normal tissues and essential organs. This study aimed to develop a novel immunotherapy targeting STEAP1/2 to elicit PCa-specific immune responses in cellular and animal mPCa models. Monoclonal antibodies were generated against the extracellular region of STEAP1, which shares 60% sequence similarity with STEAP2 but has minimal homology with other human proteins. The specificity and binding strength of these antibodies were validated through techniques such as immunofluorescence, flow cytometry, immunoprecipitation, and ELISA. Results from immunofluorescence and flow cytometry using STEAP1 overexpression and knockdown PCa cell lines demonstrated the specificity of certain clones for human STEAP1. Furthermore, one antibody clone successfully pulled down STEAP2 in immunoprecipitation-mass spectrometry experiments and showed binding to STEAP2 in cell lines overexpressing the antigen. ELISA results revealed binding affinities in the low nanomolar range for STEAP1 and the low micromolar range for STEAP2.These findings highlight the potential of the monoclonal STEAP1/2 antibody developed in this study, providing a promising platform for future immunotherapy strategies and expanding treatment options for mPCa patients. Citation Format: Minzhi Sheng, Boyang Su, Amanda Sparkes, Gobi Thillainadesan, Esther Matus, Jessica Wright, Stanley Liu, Jean Gariepy, Hon S. Leong. A novel immunotherapy for metastatic prostate cancer: A monoclonal antibody that can bind both STEAP1 and STEAP2 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4771.

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Publication Details

Journal
Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-4771
Primary Topic
Prostate Cancer Treatment and Research
Type
article
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article

Abstract 4771: A novel immunotherapy for metastatic prostate cancer: A monoclonal antibody that can bind both STEAP1 and STEAP2

Gobi Thillainadesan, Boyang Su, Jean Gariépy, Stanley K. Liu et al.
Cancer Research
Prostate Cancer Treatment and Research
article

Abstract 4771: A novel immunotherapy for metastatic prostate cancer: A monoclonal antibody that can bind both STEAP1 and STEAP2

Gobi Thillainadesan, Boyang Su, Jean Gariépy, Stanley K. Liu, Minzhi Sheng, Esther Matus, Jessica Wright, Hon S. Leong, Amanda Sparkes
article en

Abstract

Prostate cancer (PCa) is the most common cancer among Canadian men, with metastatic PCa (mPCa) patients having a 5-year survival rate of only 30%. However, the prostate-specific membrane antigen, a key target in PCa therapy, is expressed in many normal tissues and shows heterogeneity among PCa patients. Recently, Six Transmembrane Epithelial Antigens of the Prostate 1 and 2 (STEAP1 and STEAP2) have gained attention as promising therapeutic targets due to their high expression in most PCa cases compared to normal tissues and essential organs. This study aimed to develop a novel immunotherapy targeting STEAP1/2 to elicit PCa-specific immune responses in cellular and animal mPCa models. Monoclonal antibodies were generated against the extracellular region of STEAP1, which shares 60% sequence similarity with STEAP2 but has minimal homology with other human proteins. The specificity and binding strength of these antibodies were validated through techniques such as immunofluorescence, flow cytometry, immunoprecipitation, and ELISA. Results from immunofluorescence and flow cytometry using STEAP1 overexpression and knockdown PCa cell lines demonstrated the specificity of certain clones for human STEAP1. Furthermore, one antibody clone successfully pulled down STEAP2 in immunoprecipitation-mass spectrometry experiments and showed binding to STEAP2 in cell lines overexpressing the antigen. ELISA results revealed binding affinities in the low nanomolar range for STEAP1 and the low micromolar range for STEAP2.These findings highlight the potential of the monoclonal STEAP1/2 antibody developed in this study, providing a promising platform for future immunotherapy strategies and expanding treatment options for mPCa patients. Citation Format: Minzhi Sheng, Boyang Su, Amanda Sparkes, Gobi Thillainadesan, Esther Matus, Jessica Wright, Stanley Liu, Jean Gariepy, Hon S. Leong. A novel immunotherapy for metastatic prostate cancer: A monoclonal antibody that can bind both STEAP1 and STEAP2 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 4771.

Cancer ResearchVol. 85(8_Supplement_1)
Sunnybrook Hospital (CA), Sunnybrook Research Institute
Openalex Percentile: Top 87%
Prostate Cancer Treatment and Research
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