Related Resources for this page:
- Tumor Types
- Molecular Causes of Cancer
- Biological Pathways
- Therapeutic Targets
- Clinical Trials
- Cancer Biomarkers
- Breast Cancer
- A brief history of ADCs
- Breast Cancer
- Current research in ADCs
- Cytotoxic agent
- Genome instability and mutation
- Slide decks and videos
- HER2 dimerization
- How are ADCs designed to work?
- Glossary
- Monoclonal antibody
- Multimedia Resources
- Receptor-Mediated Endocytosis
- Research HDIs
- Research ADCs
- Stable linker
- Targeting cancers with ADCs
- HER2+ breast cancer
- What are ADCs?
- Ovarian Cancer
- Breast Cancer
- Future Directions
- Antibody-Drug conjugates
- Summary
- A brief history of ADCs
- Cancer effects
- Current research in ADCs
- Cytotoxic agent
- HER2
- HER ligands
- HER pathways slide decks and videos
- Glossary
- Receptor activation
- Dimerization
- HER Signaling
- Overview
- HER1/EGFR evaluation
- HER1/EGFR and prognosis
- HER1/EGFR as a therapeutic target
- Summary
- HER1/EGFR in lung cancer
- HER1/EGFR in pancreatic cancer
- HER2 dysregulation
- HER2:HER3 dimer
- HER2 and prognosis
- HER2 detection methods
- HER2 as a therapeutic target
- HER2 in breast cancer
- Summary
- HER2 in ovarian cancer
- HER3 dysregulation
- HER3
- HER3 evaluation
- HER3 as a therapeutic target
- HER3 in breast cancer
- HER3 in ovarian cancer
- HER4
- How are ADCs designed to work?
- Glossary
- Monoclonal antibody
- Multimedia Resources
- Receptor-Mediated Endocytosis
- Research ADCs
- Research MET
- Stable linker
- HER receptors
- Summary
- Targeting cancers with ADCs
- Summary
- What are ADCs?
- What is Met?
- Glycoengineered Antibodies
- Non-Antibody Biologics
- Targeted Small Molecules
- Summary
- Cancer effects
- Apoptosis
- Resisting apoptosis
- HER2
- Gastric Cancer
- HER ligands
- HER pathways slide decks and videos
- Glossary
- Receptor activation
- Dimerization
- Overview
- HER1/EGFR evaluation
- HER1/EGFR and prognosis
- HER1/EGFR as a therapeutic target
- Summary
- HER1/EGFR in lung cancer
- HER1/EGFR in pancreatic cancer
- HER2 dysregulation
- HER2:HER3 dimer
- HER2 and prognosis
- HER2 detection methods
- HER2 as a therapeutic target
- HER2 in breast cancer
- Summary
- HER2 in ovarian cancer
- HER3 dysregulation
- HER3
- HER3 evaluation
- HER3 as a therapeutic target
- HER3 in breast cancer
- HER3 in ovarian cancer
- HER4
- Glossary
- MAPK Signaling
- MEK Inhibitor (GDC-0973)
- PI3K Inhibitor (GDC-0941)
- Research MET
- HER receptors
- Summary
- PI3K/Akt/mTOR Signaling
- Slide decks and videos
- Summary
- What is Met?
- Traditional Monoclonal Antibodies
- Summary
- Cancer effects
- Glossary
- HER2
- Gastric Cancer
- HER ligands
- HER pathways slide decks and videos
- Glossary
- Receptor activation
- Dimerization
- HER Signaling
- Overview
- HER1/EGFR evaluation
- HER1/EGFR and prognosis
- HER1/EGFR as a therapeutic target
- Summary
- HER1/EGFR in lung cancer
- HER1/EGFR in pancreatic cancer
- HER2 dysregulation
- HER2:HER3 dimer
- HER2 and prognosis
- HER2 detection methods
- HER2 as a therapeutic target
- HER2 in breast cancer
- Summary
- HER2 in ovarian cancer
- HER3 dysregulation
- HER3
- HER3 evaluation
- HER3 as a therapeutic target
- HER3 in breast cancer
- HER3 in ovarian cancer
- HER4
- Research MET
- HER receptors
- Summary
- Angiogenic Signaling
- Inhibition of HER2 dimerization
- Slide decks and videos
- Summary
- What is Met?
- Antibody-Drug conjugates
Therapeutic Potential of HER Pathways
There are multiple ways to target HER pathways
Because HER signaling pathways are extremely complex, they can be targeted using several different strategies.
Ligands that bind to HER receptors, the extracellular ligand-binding domain of a HER family receptor, the intracellular tyrosine kinase domain of the receptor, and downstream molecular signals can all be targeted.1,5
HER pathways have potential as therapeutic targets in many tumor types
Because of their involvement in tumor biology, HER family receptors and their associated signaling pathways represent potential therapeutic targets. A number of strategies could be utilized to target HER pathways.
Targeting the ligand
One possible strategy involves molecules that would target ligands specific to HER family receptors.
- This strategy would prevent ligands from binding to their associated receptors, thus preventing the activation of signaling pathways1
- Note that HER2, the preferred dimerization partner for HER family receptors, does not bind ligands1
- Therefore, the strategy of targeting ligands may not be ideal
Targeting the extracellular domain of the receptor
The extracellular domain of a HER family receptor, which binds ligands (with the exception of HER2), represents another possible therapeutic target.
- Molecules such as monoclonal antibodies would bind to the extracellular domain of a HER family receptor, either suppressing receptor activity or preventing receptor dimerization12
- This would prevent phosphorylation of the tyrosine kinase domain of the receptor and therefore preclude the initiation of downstream signaling pathways
- These molecules are specific to a single type of HER family receptor
- Monoclonal antibodies may also trigger an immune response to cancer cells
Targeting the intracellular domain of the receptor
The tyrosine kinase domain of a HER family receptor is located within the cell membrane and might also be a therapeutic target.
- Small molecules can prevent transphosphorylation of the tyrosine kinase domain of dimerized HER family receptors13
- Without transactivation of dimerized receptors, downstream signaling pathways are not initiated
- These molecules could be specific to a single type of HER family receptor or have broader activity
Targeting downstream signaling pathways
Targeting molecules in the downstream signaling cascade that occurs after HER family receptors have been activated is also a potential therapeutic strategy.
- HER family receptor dimers often initiate multiple downstream signaling pathways1
- Each of these pathways might require a different molecule for therapeutic inhibition