Restoration of the Lost Human Beta Defensin-1 Protein in Cancer as a Strategy to Improve the Efficacy of Chemotherapy
Both innate and adaptive immunity are important components of the human defense system against various diseases including cancer. Human beta defensin-1 (hBD-1) is one such immunomodulatory peptide which is lost in malignant cancers, while high levels of expression are maintained in benign cells, making it a potential biomarker for the onset and metastasis of the disease. Triple-negative breast cancer (TNBC) is an aggressive form of breast cancer for which no targeted therapy has been approved so far. That makes chemotherapy a first line of treatment despite high side effects. A priori Activation of Apoptosis Pathways of Tumor often referred to as AAAPT technology is a novel targeted tumor sensitizing technology that sensitizes low responsive and resistant tumor cells to evoke a better response from the current treatments for TNBC. Here, we show that hBD-1 is a targeted tumor sensitizer.
Authors
- Ramasamy Paulmurugan (ORCID: https://orcid.org/0000-0001-7155-4738)
- Thillai V. Sekar (ORCID: https://orcid.org/0000-0002-2919-8802)
- Raghu S. Pandurangi (ORCID: https://orcid.org/0000-0002-8143-2627)
Institutions
- Stanford University (US)
Publication Details
- Journal
- Journal of Medicinal Chemistry
- Published
- 2024-08-13
- DOI
- https://doi.org/10.1021/acs.jmedchem.4c01040
- Citations
- 2
- Primary Topic
- Antimicrobial Peptides and Activities
- Type
- article
- Field-Weighted Citation Impact
- 0.69
Funders
- National Institutes of Health