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A Real-time Potency Assay for Chimeric Antigen Receptor T Cells Targeting Solid and Hematological Cancer Cells
Published on: November 12, 2019
Cell-Surface GRP78-Targeted Chimeric Antigen Receptor T Cells Eliminate Lung Cancer Tumor Xenografts
Shijie Wang1, Wenwen Wei1, Yuncang Yuan1
1Department of Targeting Therapy & Immunology and Laboratory of Animal Tumor Models, Cancer Center and State Key Laboratory of Respiratory Health and Multimorbidity and Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu 610041, China.
Abstract:
Lung cancer is one of the most common and intractable malignancies. It is associated with low survival rates despite existing treatments, indicating that new and more effective therapies are urgently needed such as the chimeric antigen receptor-T (CAR-T) cell immunotherapy. The cell-surface glucose-regulated protein 78 (csGRP78) is expressed in various hematological malignancies and solid tumor cells including lung cancer in response to cancer-related endoplasmic reticulum stress, while GRP78 is restricted to inside the normal cells. Here, we detected the prominent expression of csGRP78 in both lung cancer cell lines, A549 and H1299, as well as cancer stemlike cells derived from A549 by immunofluorescence. Next, a csGRP78-targeted CAR was constructed, and the transduced CAR-T cells were tested for their potency to kill the two lung cancer cell lines and derived stemlike cells, which was correlated with specific interferon γ release in vitro. Finally, we found that csGRP78 CAR-T cells also efficiently killed both lung cancer cells and cancer stemlike cells, resulting into the elimination of tumor xenografts in vivo, neither with any evidence of relapse after 63 days of tumor clearance nor any detrimental impact on other body organs we examined. Our study reveals the capacity of csGRP78 as a therapeutic target and offers valuable insight into the development of csGRP78 CAR-T cells as potential therapy for lung cancer.
Insights
Chimeric antigen receptor-T (CAR-T) cell therapy targeting cell-surface glucose-regulated protein 78 (csGRP78) shows promise for lung cancer. This novel therapy effectively eliminated lung tumors in vivo without relapse or organ damage.
Area of Science:
- Oncology
- Immunotherapy
- Cell Biology
Background:
- Lung cancer has low survival rates despite current treatments.
- Novel therapies like CAR-T cell immunotherapy are urgently needed.
- Cell-surface glucose-regulated protein 78 (csGRP78) is a potential cancer target, expressed on lung cancer cells but not normal cells.
Purpose of the Study:
- To investigate csGRP78 as a therapeutic target for lung cancer.
- To develop and evaluate csGRP78-targeted CAR-T cells for lung cancer treatment.
Main Methods:
- Detected csGRP78 expression in lung cancer cell lines and cancer stem-like cells.
- Constructed csGRP78-targeted CAR and transduced T cells.
- Assessed CAR-T cell efficacy against lung cancer cells and xenografts in vitro and in vivo.
Main Results:
- csGRP78 was prominently expressed on lung cancer cells and cancer stem-like cells.
- csGRP78 CAR-T cells demonstrated potent killing of lung cancer cells and stem-like cells in vitro, with interferon γ release.
- csGRP78 CAR-T cells eradicated lung tumor xenografts in vivo without relapse or observed organ toxicity.
Conclusions:
- csGRP78 is a viable therapeutic target for lung cancer.
- csGRP78 CAR-T cells represent a promising new immunotherapy for lung cancer with a favorable safety profile.
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