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Updated: Aug 9, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Endoglin (CD105) is a target for an oral DNA vaccine against breast cancer
Sung-Hyung Lee1, Noriko Mizutani, Masato Mizutani
1Department of Immunology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Abstract:
Endoglin (CD105), a co-receptor in the TGF-beta receptor complex, is over-expressed on proliferating endothelial cells in the breast tumor neovasculature and thus offers an attractive target for anti-angiogenic therapy. Here we report the anti-angiogenic/anti-tumor effects achieved in a prophylactic setting with an oral DNA vaccine encoding murine endoglin, carried by double attenuated Salmonella typhimurium (dam-, AroA-) to a secondary lymphoid organ, i.e., Peyer's patches . We demonstrate that an endoglin vaccine elicited activation of antigen-presenting dendritic cells, coupled with immune responses mediated by CD8+ T cells against endoglin-positive target cells. Moreover, we observed suppression of angiogenesis only in mice administered with the endoglin vaccine as compared to controls. These data suggest that a CD8+ T cell-mediated immune response induced by this vaccine effectively suppressed dissemination of pulmonary metastases of D2F2 breast carcinoma cells presumably by eliminating proliferating endothelial cells in the tumor vasculature. It is anticipated that vaccine strategies such as this may contribute to future therapies for breast cancer.
Insights
An oral DNA vaccine targeting endoglin (CD105) suppressed breast cancer growth and metastasis in mice. This anti-angiogenic therapy activated CD8+ T cells to eliminate tumor vasculature, offering a potential new breast cancer treatment.
Area of Science:
- Immunology
- Oncology
- Vascular Biology
Background:
- Endoglin (CD105) is over-expressed on breast tumor neovasculature, making it a target for anti-angiogenic therapy.
- Targeting tumor angiogenesis is a key strategy in cancer treatment.
Purpose of the Study:
- To evaluate the anti-angiogenic and anti-tumor effects of an oral DNA vaccine encoding murine endoglin.
- To investigate the immune mechanisms underlying the vaccine's efficacy.
Main Methods:
- An oral DNA vaccine encoding murine endoglin was delivered via attenuated Salmonella typhimurium to Peyer's patches.
- Immune responses, including CD8+ T cell activation and dendritic cell activity, were assessed.
- Angiogenesis and tumor metastasis were evaluated in a prophylactic setting using D2F2 breast carcinoma cells in mice.
Main Results:
- The endoglin vaccine activated antigen-presenting dendritic cells and elicited CD8+ T cell responses against endoglin-positive cells.
- Significant suppression of angiogenesis was observed in mice receiving the endoglin vaccine compared to controls.
- The vaccine effectively suppressed pulmonary metastasis of breast carcinoma cells.
Conclusions:
- A CD8+ T cell-mediated immune response induced by the endoglin DNA vaccine can suppress tumor angiogenesis and metastasis.
- This vaccine strategy shows promise for future breast cancer therapies by targeting tumor vasculature.
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