Related Experiment Video
Updated: Apr 26, 2026

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
Pancreatic cancer: Hurdles in the engineering of CAR-based immunotherapies
Daniel Abate-Daga1, Steven A Rosenberg1, Richard A Morgan2
1Surgery Branch; Center for Cancer Research; National Cancer Institute; Bethesda, MD USA.
Abstract:
Pancreatic cancer remains largely an incurable disease necessitating the development of novel therapeutic approaches. Adoptive immunotherapy using chimeric antigen receptor (CAR)-transduced T cells represents an alternative treatment with curative potential. We present an overview of the engineering of novel CARs targeting prostate stem cell antigen (PSCA), implications for the development of immunotherapies, and potential strategies to circumvent on-target/off-tumor toxicities.
Insights
Pancreatic cancer is hard to treat, but new immunotherapies show promise. Researchers are developing chimeric antigen receptor (CAR) T-cell therapies targeting prostate stem cell antigen (PSCA) to improve treatment and reduce side effects.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Pancreatic cancer is a significant unmet medical need with limited effective treatments.
- Adoptive immunotherapy, particularly chimeric antigen receptor (CAR)-T cell therapy, offers a promising avenue for cancer treatment.
- Targeting specific antigens on cancer cells is crucial for effective immunotherapy.
Purpose of the Study:
- To review the engineering of novel CARs targeting prostate stem cell antigen (PSCA).
- To discuss the implications of PSCA-targeted CARs for pancreatic cancer immunotherapy development.
- To explore strategies for mitigating on-target/off-tumor toxicities associated with CAR-T cell therapy.
Main Methods:
- Review of current literature on CAR engineering and pancreatic cancer targets.
- Analysis of PSCA as a potential target for CAR-T cell therapy in pancreatic cancer.
- Discussion of potential CAR designs and delivery strategies.
- Exploration of methods to enhance CAR-T cell specificity and safety.
Main Results:
- PSCA is identified as a promising target antigen for pancreatic cancer immunotherapy.
- Novel CAR constructs targeting PSCA are being developed.
- Strategies to manage potential toxicities are being investigated.
Conclusions:
- PSCA-targeted CAR-T cell therapy holds potential as a novel treatment for pancreatic cancer.
- Further research is needed to optimize CAR design and therapeutic strategies to ensure safety and efficacy.
Related Concept Videos
Tumor Immunotherapy
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...

