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The Use of Reverse Phase Protein Arrays (RPPA) to Explore Protein Expression Variation within Individual Renal Cell Cancers
Published on: January 22, 2013
Antigenic targets for renal cell carcinoma immunotherapy
Johannes Vieweg1, Andrew Jackson
1Duke University Medical Center, MSRB, Suite 455, PO Box 2626, Durham, North Carolina 27710, USA. j.vieweg@duke.edu
Abstract:
Renal cell carcinoma (RCC) has been shown to respond to immunotherapeutic intervention, thus fostering continued interest in exploiting the ability of the immune system to recognise and eradicate renal malignancy. Considerable progress in the characterisation of tumour-associated antigens, coupled with the appreciation that dendritic cells act as master regulators of immunity and tolerance, has opened new possibilities for immunotherapeutic intervention against human cancer. However, in contrast to other tumour systems, clinically relevant antigens expressed by RCC have not yet been identified. Therefore, most RCC vaccine trials have employed unfractionated antigens derived from tumour cells, with the goal of eliciting T cell responses against many unknown antigens expressed by the tumour. The recent discovery of genes with critical roles in oncogenesis has facilitated the identification of novel, more universal targets that may make cancer vaccines more practical, applicable and, potentially, more effective. In addition, immunisation against tumour antigens can be combined with tumour stroma-associated targets, thereby exerting a synergistic antitumour effect. Continued identification of molecular targets, in concert with more effective vaccination protocols, is likely to produce vaccination strategies with clinical impact.
Insights
Immunotherapy shows promise for renal cell carcinoma (RCC). Identifying novel tumor antigens and refining vaccination strategies are key to developing effective cancer vaccines for RCC.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Renal cell carcinoma (RCC) demonstrates responsiveness to immunotherapy, stimulating research into immune-based eradication of kidney cancer.
- Advances in characterizing tumor-associated antigens and understanding dendritic cell roles in immunity offer new avenues for cancer immunotherapy.
Purpose of the Study:
- To explore the potential of novel molecular targets and improved vaccination protocols for enhancing immunotherapeutic interventions against renal cell carcinoma.
- To address the challenge of identifying clinically relevant antigens specific to RCC, which have remained elusive compared to other cancer types.
Main Methods:
- Review of progress in tumor-associated antigen characterization.
- Analysis of the role of dendritic cells in immune regulation.
- Exploration of novel targets arising from oncogenesis gene discovery.
- Consideration of combination strategies involving tumor antigens and stroma-associated targets.
Main Results:
- While clinically relevant RCC antigens are not yet identified, most RCC vaccine trials use unfractionated tumor antigens to elicit T cell responses.
- The discovery of oncogenesis-related genes provides opportunities for identifying more universal and effective cancer vaccine targets.
- Combining immunizations against tumor antigens with stroma-associated targets may yield synergistic anti-tumor effects.
Conclusions:
- Continued identification of molecular targets is crucial for advancing RCC immunotherapy.
- Development of more effective vaccination protocols, potentially targeting novel antigens and stroma, is likely to lead to clinically impactful vaccination strategies for renal cell carcinoma.
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