An apolipoprotein A-I mimetic targets scavenger receptor A on tumor-associated macrophages: A prospective anticancer treatment?
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A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Claudine Neyen1, Subhankar Mukhopadhyay, Siamon Gordon
1Sir William Dunn School of Pathology; University of Oxford; Oxford, UK.
Abstract:
Tumor-associated macrophages polarize toward an M2 phenotype and express scavenger receptor A (SRA), hence promoting tumor progression. We demonstrated that SRA can be therapeutically targeted in vivo with the small peptide inhibitor 4F to prevent metastatic spread. Beyond our study, 4F is emerging as a promising anticancer agent.
Insights
Tumor-associated macrophages promote cancer spread by expressing scavenger receptor A (SRA). Targeting SRA with the peptide 4F in vivo effectively prevented metastasis, showing 4F
Area of Science:
- Immunology
- Oncology
- Molecular Biology
Background:
- Tumor-associated macrophages (TAMs) often adopt an M2 phenotype.
- M2-polarized TAMs express scavenger receptor A (SRA), contributing to tumor progression and metastasis.
Purpose of the Study:
- To investigate the therapeutic potential of targeting SRA in vivo.
- To evaluate the efficacy of the small peptide inhibitor 4F in preventing cancer metastatic spread.
Main Methods:
- In vivo studies utilizing the peptide inhibitor 4F.
- Assessment of SRA targeting and its effect on metastatic spread.
Main Results:
- Demonstrated successful in vivo therapeutic targeting of SRA.
- The peptide inhibitor 4F effectively prevented tumor metastatic spread.
Conclusions:
- Scavenger receptor A (SRA) is a viable therapeutic target in cancer.
- The small peptide inhibitor 4F shows promise as an anticancer agent for preventing metastasis.
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