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Published on: July 29, 2017
Cripto-1 Plasmid DNA Vaccination Targets Metastasis and Cancer Stem Cells in Murine Mammary Carcinoma
Kristina Witt1, Maarten A Ligtenberg1, Laura Conti2
1Department of Oncology and Pathology, Cancer Center Karolinska, Karolinska Institutet, Stockholm, Sweden.
Abstract:
Metastatic breast cancer is a fatal disease that responds poorly to treatment. Cancer vaccines targeting antigens expressed by metastatic breast cancer cells and cancer stem cells could function as anticancer therapies. Cripto-1 is an oncofetal protein overexpressed in invasive breast cancer and cancer-initiating cells. In this study, we explored the potential of a Cripto-1-encoding DNA vaccine to target breast cancer in preclinical mouse models. BALB/c mice and BALB-neuT mice were treated with a DNA vaccine encoding mouse Cripto-1 (mCr-1). BALB/c mice were challenged with murine breast cancer 4T1 cells or TUBO spheres; BALB-neuT mice spontaneously developed breast cancer. Tumor growth was followed in all mouse models and lung metastases were evaluated. In vitro assays were performed to identify the immune response elicited by vaccination. Vaccination against mCr-1 reduced primary tumor growth in the 4T1 metastatic breast cancer model and reduced lung metastatic burden. In BALB-neuT mice, because the primary tumors are Cripto-1 negative, vaccination against mCr-1 did not affect primary tumors but did reduce lung metastatic burden. Spheroid-cultured TUBO cells, derived from a BALB/neuT primary tumor, develop a cancer stem cell-like phenotype and express mCr-1. We observed reduced tumor growth in vaccinated mice after challenge with TUBO spheres. Our data indicate that vaccination against Cripto-1 results in a protective immune response against mCr-1 expressing and metastasizing cells. Targeting Cripto-1 by vaccination holds promise as an immunotherapy for treatment of metastatic breast cancer. Cancer Immunol Res; 6(11); 1417-25. ©2018 AACR.
Insights
A DNA vaccine targeting Cripto-1 showed promise in reducing tumor growth and metastasis in preclinical breast cancer models. This immunotherapy approach offers a potential new strategy for treating metastatic breast cancer by targeting Cripto-1 expressing cells.
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Metastatic breast cancer remains a significant challenge due to poor treatment response.
- Cancer vaccines offer a potential therapeutic strategy by targeting cancer-specific antigens.
- Cripto-1, an oncofetal protein, is overexpressed in invasive breast cancer and cancer stem cells.
Purpose of the Study:
- To evaluate the efficacy of a DNA vaccine encoding mouse Cripto-1 (mCr-1) in preclinical mouse models of breast cancer.
- To assess the vaccine's impact on primary tumor growth and metastatic burden.
- To investigate the immune response generated by the Cripto-1 DNA vaccine.
Main Methods:
- BALB/c and BALB-neuT mice were vaccinated with an mCr-1 DNA vaccine.
- Mice were challenged with 4T1 breast cancer cells or TUBO spheres, or developed spontaneous tumors (BALB-neuT).
- Tumor growth, lung metastasis, and in vitro immune responses were analyzed.
Main Results:
- Vaccination against mCr-1 reduced primary tumor growth and lung metastasis in the 4T1 model.
- In BALB-neuT mice, mCr-1 vaccination reduced lung metastasis despite Cripto-1 negative primary tumors.
- Vaccination also reduced tumor growth in mice challenged with Cripto-1 expressing TUBO spheres.
Conclusions:
- Cripto-1 DNA vaccination elicits a protective immune response against mCr-1 expressing and metastasizing cells.
- Targeting Cripto-1 via vaccination demonstrates potential as an immunotherapy for metastatic breast cancer.
- This approach holds promise for overcoming treatment resistance in advanced breast cancer.
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