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Updated: Apr 2, 2026

Modeling Breast Cancer via an Intraductal Injection of Cre-expressing Adenovirus into the Mouse Mammary Gland
Published on: June 7, 2019
An In silico Chimeric Vaccine Targeting Breast Cancer Containing Inherent Adjuvant
Abbas Ali Imani Fooladi1, Hamideh Mahmoodzadeh Hosseini1, Jafar Amani1
1Applied Microbiology Research Center, Baqiyatallah University of Medical Sciences, Tehran, IR Iran.
Background:
Today, Lack of efficient therapeutic strategy for breast cancer (the most common cause of death in women) is one of the momentous problematic topics for all health care committees. Designing new specific vaccine, based on antigens located on the surface of cancer cells can be useful. Over expression of ROR1, lacked of HER2/neu, and hormone receptors on cell surface in the breast cancer, introduce this protein as an appropriate candidate for designing cancer vaccine.
Objectives:
We hypothesized the extracellular domain of receptor tyrosine kinase like orphan receptor 1 (ROR-1) along with a super antigen such as staphylococcal enterotoxin B could be a potent vaccine for drug resistant breast cancer.
Materials And Methods:
Here, we assessed the findings of bioinformatics analysis to identify the antitumor immune properties of this chimeric construct. In addition, the stability, physic-chemical properties and allergic potency of designed fusion protein were investigated by valid bioinformatics software.
Results:
Our result suggested that chimeric model is capable to be a stimulant of both T-cell and B- cell mediated immune responses with an acceptable accessibility and solubility but without any allergenicity.
Conclusions:
The ROR-1 with an enterotoxin B could be a potent vaccine for breast cancer.
Insights
A novel breast cancer vaccine combining Receptor Tyrosine Kinase Like Orphan Receptor 1 (ROR1) with staphylococcal enterotoxin B shows promise. This chimeric construct stimulates immune responses without allergenicity, offering a potential strategy against drug-resistant breast cancer.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Breast cancer remains a leading cause of death in women, necessitating novel therapeutic strategies.
- The over expression of ROR1 on breast cancer cells, in the absence of HER2/neu and hormone receptors, makes it a viable target for vaccine development.
- Current therapeutic options for breast cancer are limited, particularly for drug-resistant forms.
Purpose of the Study:
- To investigate the potential of a chimeric vaccine construct comprising the extracellular domain of ROR1 and staphylococcal enterotoxin B (SEB) for treating drug-resistant breast cancer.
- To evaluate the antitumor immune properties, stability, physicochemical characteristics, and allergenicity of the designed ROR1-SEB fusion protein using bioinformatics analysis.
Main Methods:
- Bioinformatics analysis was employed to assess the antitumor immune properties of the ROR1-SEB chimeric construct.
- In silico methods were used to investigate the stability, physicochemical properties, and potential allergenicity of the designed fusion protein.
Main Results:
- The chimeric ROR1-SEB construct demonstrated potential as a stimulant for both T-cell and B-cell mediated immune responses.
- Bioinformatics analysis indicated acceptable accessibility and solubility for the designed fusion protein.
- The study found no evidence of allergenicity associated with the ROR1-SEB fusion protein.
Conclusions:
- The ROR1-SEB fusion protein holds promise as a potent vaccine candidate for breast cancer.
- This chimeric approach offers a potential new avenue for developing effective treatments against drug-resistant breast cancer.
- Further research into this ROR1-based vaccine strategy is warranted.
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Published on: March 26, 2014
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Published on: February 10, 2023
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