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Published on: July 5, 2019
Genetically engineered fusion proteins for treatment of cancer
Ulrich H Weidle1, Britta Schneider, Guy Georges
1Roche Pharma Research and Early Development (pRED), Roche Diagnostics GmbH, Im Nonnenwald 2, D-82372 Penzberg, Germany. ulrich.weidle@roche.com
Abstract:
In this review, we summarize approaches to treat cancer with genetically engineered fusion proteins. Such proteins can act as decoy receptors for several ligands or as recruiters of immune effector cells to tumor. Examples of interference with growth factor-mediated tumor growth and tumor-related angiogenesis with fusion proteins consisting of the extracellular domains, and in some cases also of entities of one or several receptors and the Fc part of human IgG1, are discussed. In addition, we present strategies for recruitment of immune effector cells to tumor with fusion proteins. This can be achieved with fusion proteins consisting of a tumor-related antibody and a cytokine or major histocompatibilty complex class-I-peptide complexes, by T-cell receptor cytokine fusion proteins or by combination of a T-cell-recruiting antibody with a tumor-related ligand or a defined T-cell receptor.
Insights
Genetically engineered fusion proteins offer novel cancer treatment strategies by acting as decoy receptors or immune cell recruiters. These engineered proteins target tumor growth and angiogenesis, showing promise in immunotherapy.
Area of Science:
- Biotechnology
- Immunology
- Oncology
Background:
- Cancer growth and angiogenesis are complex processes often driven by specific growth factors.
- Current cancer therapies face challenges in specificity and efficacy.
- Genetically engineered fusion proteins represent a promising area of therapeutic development.
Purpose of the Study:
- To review current strategies for treating cancer using genetically engineered fusion proteins.
- To highlight the dual role of fusion proteins as decoy receptors and immune cell recruiters.
- To discuss specific examples and future directions in fusion protein-based cancer therapy.
Main Methods:
- Review of existing literature on fusion protein applications in cancer treatment.
- Analysis of fusion protein designs targeting growth factor receptors and angiogenesis.
- Examination of strategies for recruiting immune effector cells to tumors using engineered proteins.
Main Results:
- Fusion proteins can effectively interfere with growth factor-mediated tumor growth and angiogenesis.
- Engineered proteins incorporating receptor extracellular domains and Fc regions show therapeutic potential.
- Strategies for immune cell recruitment include antibody-cytokine fusions and T-cell receptor-based constructs.
Conclusions:
- Genetically engineered fusion proteins offer versatile approaches for cancer treatment.
- These proteins can modulate tumor microenvironments and enhance anti-tumor immunity.
- Further research into fusion protein design and application holds significant promise for oncology.
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