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Evaluating the Effectiveness of Cancer Drug Sensitization In Vitro and In Vivo
Published on: February 6, 2015
Abscopal Effect and Drug-Induced Xenogenization: A Strategic Alliance in Cancer Treatment?
Ornella Franzese1, Francesco Torino2, Elisa Giannetti2
1School of Medicine, Department of Systems Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.
Abstract:
The current state of cancer treatment is still far from being satisfactory considering the strong impairment of patients' quality of life and the high lethality of malignant diseases. Therefore, it is critical for innovative approaches to be tested in the near future. In view of the crucial role that is played by tumor immunity, the present review provides essential information on the immune-mediated effects potentially generated by the interplay between ionizing radiation and cytotoxic antitumor agents when interacting with target malignant cells. Therefore, the radiation-dependent abscopal effect (i.e., a biological effect of ionizing radiation that occurs outside the irradiated field), the influence of cancer chemotherapy on the antigenic pattern of target neoplastic cells, and the immunogenic cell death (ICD) caused by anticancer agents are the main topics of this presentation. It is widely accepted that tumor immunity plays a fundamental role in generating an abscopal effect and that anticancer drugs can profoundly influence not only the host immune responses, but also the immunogenic pattern of malignant cells. Remarkably, several anticancer drugs impact both the abscopal effect and ICD. In addition, certain classes of anticancer agents are able to amplify already expressed tumor-associated antigens (TAA). More importantly, other drugs, especially triazenes, induce the appearance of new tumor neoantigens (TNA), a phenomenon that we termed drug-induced xenogenization (DIX). The adoption of the abscopal effect is proposed as a potential therapeutic modality when properly applied concomitantly with drug-induced increase in tumor cell immunogenicity and ICD. Although little to no preclinical or clinical studies are presently available on this subject, we discuss this issue in terms of potential mechanisms and therapeutic benefits. Upcoming investigations are aimed at evaluating how chemical anticancer drugs, radiation, and immunotherapies are interacting and cooperate in evoking the abscopal effect, tumor xenogenization and ICD, paving the way for new and possibly successful approaches in cancer therapy.
Insights
Innovative cancer therapies leverage tumor immunity by combining radiation and chemotherapy. This approach aims to enhance the abscopal effect and immunogenic cell death, potentially leading to new treatment strategies.
Area of Science:
- Oncology
- Immunology
- Radiation Oncology
Background:
- Current cancer treatments significantly impair patient quality of life and have high mortality rates, necessitating innovative therapeutic approaches.
- Tumor immunity plays a critical role in cancer progression and treatment response.
- Understanding immune-mediated effects of combined therapies is crucial for developing novel cancer treatments.
Purpose of the Study:
- To review the immune-mediated effects of ionizing radiation and cytotoxic chemotherapy on malignant cells.
- To explore the abscopal effect, chemotherapy's influence on tumor antigenicity, and drug-induced immunogenic cell death (ICD).
- To discuss the potential of combining these effects for novel cancer therapeutic strategies.
Main Methods:
- Review of existing literature on radiation therapy, chemotherapy, tumor immunity, abscopal effect, and immunogenic cell death.
- Analysis of how anticancer drugs modulate tumor-associated antigens (TAA) and induce neoantigens (TNA) through drug-induced xenogenization (DIX).
- Discussion of potential mechanisms and therapeutic benefits of combining abscopal effect with drug-induced immunogenicity and ICD.
Main Results:
- Anticancer drugs can influence host immune responses and the immunogenic profile of cancer cells.
- Certain drugs enhance existing tumor-associated antigens (TAA) and induce new tumor neoantigens (TNA) via DIX.
- The abscopal effect, ICD, and DIX are interconnected phenomena with potential for synergistic therapeutic outcomes.
Conclusions:
- Combining the abscopal effect with chemotherapy-induced increase in tumor cell immunogenicity and ICD presents a promising therapeutic strategy.
- Further preclinical and clinical investigations are needed to evaluate the efficacy and mechanisms of these combined approaches.
- This integrated strategy holds potential for developing new and successful cancer therapies.
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