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Updated: Sep 13, 2026

Quantification of Breast Cancer Cell Invasiveness Using a Three-dimensional (3D) Model
Published on: June 11, 2014
Comparative transductions of breast cancer cells by three DNA viruses
Annick Lucas1, Eric J Kremer, Silvio Hemmi
1INSERM U540 Molecular and Cellular Endocrinology of Cancers, 60, rue de Navacelles, Montpellier 34090, France.
Abstract:
Defining the ideal vectors to transduce breast cancer using viruses is currently under intense pre-clinical evaluation. Our study constitutes the first direct comparison of the infection efficiencies of a human serotype 5 (Ad5), a canine serotype 2 (CAV-2) adenovirus, and a human serotype 2 adeno-associated virus (AAV-2) in breast cancer cells. We observed an excellent infection efficiency for Ad5 vector, whereas both CAV-2 and AAV-2 vectors lead to low infection of these cells. Real-time PCR, flow cytometry, and antibody blocking studies suggest that Ad5 and CAV-2 infection ability is not strictly dependent on coxsackie adenovirus receptor (CAR) or alpha(v) integrin levels. In conclusion, our data suggest that human adenoviruses are excellent transducers of breast cancer cells, though it may be difficult to predict the extent of infection solely on CAR or alpha(v) integrin levels.
Insights
Human adenoviruses, such as Ad5, efficiently infect breast cancer cells, outperforming canine adenovirus (CAV-2) and adeno-associated virus (AAV-2). Viral infection efficiency may not solely depend on CAR or integrin levels.
Area of Science:
- Oncology
- Virology
- Gene Therapy
Background:
- Developing effective viral vectors for breast cancer treatment is a key area of pre-clinical research.
- Understanding vector tropism and infection efficiency is crucial for optimizing gene delivery strategies.
Purpose of the Study:
- To directly compare the infection efficiencies of human adenovirus serotype 5 (Ad5), canine adenovirus serotype 2 (CAV-2), and human adeno-associated virus serotype 2 (AAV-2) in breast cancer cells.
- To investigate the role of coxsackie adenovirus receptor (CAR) and alpha(v) integrin in mediating viral entry.
Main Methods:
- Real-time PCR to quantify viral genome in infected cells.
- Flow cytometry to assess cell surface receptor expression.
- Antibody blocking assays to determine receptor-mediated entry.
Main Results:
- Ad5 demonstrated excellent infection efficiency in breast cancer cells.
- CAV-2 and AAV-2 exhibited low infection efficiencies.
- Ad5 and CAV-2 infection did not strictly correlate with CAR or alpha(v) integrin levels.
Conclusions:
- Human adenoviruses, particularly Ad5, are highly effective at transducing breast cancer cells.
- Predicting viral vector infection efficiency based solely on CAR or alpha(v) integrin expression may be unreliable.
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