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Variable expression of coxsackie-adenovirus receptor in thyroid tumors: implications for adenoviral gene therapy
Derek K Marsee1, Douangsone D Vadysirisack, Carl D Morrison
1Medical Scientist Program, The Ohio State University, Columbus, Ohio, USA.
Abstract:
Adenoviral gene therapy represents a novel approach for the treatment of aggressive thyroid carcinomas. Both coxsackie-adenovirus receptor (CAR) and integrins have been shown to be the major determinants for adenoviral infectivity in many types of cancer cells, yet conflicting results have been reported. In this report we examine these factors mediating adenoviral infection in thyroid cells and to evaluate CAR expression in various types of thyroid cancer. We found that neither expression levels of CAR nor integrins are solely predictive of adenoviral infectivity in thyroid cells. However, the absence of CAR was associated with poor adenoviral infectivity in immortalized rat FRTL-5 cells. Moreover, preincubation with alpha-CAR antibody decreased infectivity in FTC 238 cells, a human thyroid tumor line. These results indicate that CAR does play a role in adenoviral infection of thyroid cells. Immunohistochemical analysis revealed that CAR is expressed at the cell surface in the majority of malignant thyroid tumors. We further show that adenoviral infectivity in some thyroid cancer cells can be improved by poly-L-lysine. Our study warrants a functional method to evaluate adenoviral infectivity should be developed and instituted prior to clinical trials of adenoviral gene therapy in patients with advanced thyroid cancer.
Insights
Adenoviral gene therapy shows promise for thyroid cancer. While coxsackie-adenovirus receptor (CAR) and integrins influence infection, CAR plays a role, especially when absent. Further evaluation is needed before clinical trials.
Area of Science:
- Oncology
- Virology
- Gene Therapy
Background:
- Adenoviral gene therapy is a potential treatment for aggressive thyroid carcinomas.
- Adenoviral infectivity is influenced by coxsackie-adenovirus receptor (CAR) and integrins, but results vary across cancer types.
Purpose of the Study:
- To investigate CAR and integrin roles in thyroid cell adenoviral infection.
- To assess CAR expression in diverse thyroid cancer types.
Main Methods:
- Examined adenoviral infectivity in thyroid cells.
- Evaluated CAR and integrin expression.
- Used immunohistochemistry for CAR analysis.
- Tested poly-L-lysine to enhance infectivity.
Main Results:
- Neither CAR nor integrin levels alone predict adenoviral infectivity in thyroid cells.
- Absence of CAR correlated with poor infectivity in rat FRTL-5 cells.
- Alpha-CAR antibody reduced infectivity in FTC 238 human thyroid tumor cells, indicating CAR's role.
- CAR is expressed on the cell surface of most malignant thyroid tumors.
- Poly-L-lysine improved adenoviral infectivity in some thyroid cancer cells.
Conclusions:
- CAR plays a role in adenoviral infection of thyroid cells, despite variable infectivity.
- CAR is expressed in the majority of malignant thyroid tumors.
- Developing functional methods to assess adenoviral infectivity is crucial before clinical trials for advanced thyroid cancer.
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