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Updated: Aug 29, 2026

A Nonviral Approach to Generate Transient Chimeric Antigen Receptor T Cells Using mRNA for Cancer Immunotherapy
Published on: February 21, 2025
Targeted cancer therapy with gonadotropin-releasing hormone chimeric proteins
Ahmi Ben-Yehudah1, Haya Lorberboum-Galski
1Department of Cellular Biochemistry and Human Genetics, Hebrew University, Hadassah Medical School, Jerusalem, 91120, Israel. ahmi@md.huji.ac.il
Abstract:
Tumor-associated antigens (TAAs) have been identified mainly to determine cancer prognosis. In the past few years, TAAs have been used in the development of treatment modalities such as tumor vaccination. This review describes an additional application of TAAs: as a target for specific antitumor treatment. Since TAAs are overexpressed on the tumor cell surface, they can be targeted to deliver drugs directly to cancer cells. One such delivery system exploits chimeric proteins. Chimeric proteins are a class of targeted molecules designed to recognize and specifically destroy cells that overexpress specific receptors. These molecules, designed and constructed by gene fusion techniques, comprise both cell-targeting and cell-killing moieties. The authors' laboratory has developed a number of chimeric proteins using gonadotropin-releasing hormone (GnRH) as the targeting moiety. These chimeras recognize a GnRH binding site that is expressed on adenocarcinoma cells. GnRH was fused to a large number of killing moieties, including bacterial and human proapoptotic proteins. All GnRH-based chimeric proteins selectively killed adenocarcinoma cells both in vitro and in vivo. Utilizing chimeric proteins for targeted therapy represents a new and exciting therapeutic modality for the treatment of cancer in humans.
Insights
This review explores using tumor-associated antigens (TAAs) for targeted cancer therapy. Chimeric proteins targeting GnRH receptors on adenocarcinoma cells show promise for selective cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Biotechnology
Background:
- Tumor-associated antigens (TAAs) are key in cancer prognosis and vaccine development.
- TAAs' overexpression on tumor cells enables targeted drug delivery.
- Chimeric proteins offer a novel approach for targeted cancer therapy.
Purpose of the Study:
- To review the application of TAAs as targets for specific antitumor treatments.
- To highlight the development and efficacy of GnRH-based chimeric proteins for adenocarcinoma therapy.
Main Methods:
- Gene fusion techniques to create chimeric proteins with targeting and killing moieties.
- Utilizing gonadotropin-releasing hormone (GnRH) as the targeting moiety.
- Testing GnRH-based chimeric proteins against adenocarcinoma cells in vitro and in vivo.
Main Results:
- GnRH-based chimeric proteins selectively target and recognize GnRH binding sites on adenocarcinoma cells.
- These chimeric proteins demonstrated selective killing of adenocarcinoma cells in vitro.
- Effective in vivo antitumor activity was observed with GnRH-based chimeric proteins.
Conclusions:
- Chimeric proteins utilizing TAAs represent a promising new therapeutic strategy for cancer.
- Targeted delivery of cytotoxic agents via GnRH-based chimeras offers a selective approach to cancer treatment.
- This modality holds potential for human cancer therapy.
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