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Updated: Aug 21, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Targeting ErbB receptor signaling: a pan-ErbB approach to cancer
1Division of Hematology/Oncology, Department of Medicine, David Geffen School of Medicine at University of California at Los Angeles, 10945 Le Conte Avenue, Los Angeles, CA 90095, USA. cbritten@mednet.ucla.edu
Abstract:
The ErbB receptors are localized to the cell membrane where they are activated by ligand to trigger a network of signaling pathways. In some cancer cells, dysregulation of ErbB-mediated signaling confers a growth advantage, resulting in cellular transformation and increased metastatic potential. Several agents that inhibit individual ErbB receptors have recently been approved for the treatment of human malignancies, validating ErbB receptors as therapeutic targets. One strategy to improve the efficacy of ErbB-targeted therapies is to inhibit multiple ErbB receptors, thereby interfering with the cooperation that exists between receptors. This minireview addresses the approaches being developed to concurrently inhibit multiple ErbB receptors.
Insights
Targeting multiple ErbB receptors simultaneously may improve cancer therapy. This review explores strategies for concurrently inhibiting these key signaling proteins to overcome treatment resistance.
Area of Science:
- Oncology
- Molecular Biology
- Cell Signaling
Background:
- ErbB receptors are key regulators of cell growth and survival.
- Dysregulated ErbB signaling drives cancer progression and metastasis.
- Current therapies target individual ErbB receptors with limited efficacy.
Purpose of the Study:
- To review emerging strategies for concurrently inhibiting multiple ErbB receptors.
- To highlight the therapeutic potential of multi-targeting ErbB-directed therapies.
Main Methods:
- Literature review of preclinical and clinical studies.
- Analysis of signaling pathways involving ErbB receptor cooperation.
- Evaluation of therapeutic approaches targeting multiple ErbB receptors.
Main Results:
- ErbB receptor family members exhibit cooperative signaling in cancer.
- Concurrent inhibition of multiple ErbB receptors shows promise in preclinical models.
- Development of novel agents targeting multiple ErbB receptors is ongoing.
Conclusions:
- Simultaneous inhibition of multiple ErbB receptors represents a promising therapeutic strategy.
- Overcoming resistance to ErbB-targeted therapies may be achieved through multi-targeting approaches.
- Further research is needed to optimize combination therapies involving multiple ErbB inhibitors.
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