Antibody-drug conjugates targeting SSEA-4 inhibits growth and migration of SSEA-4 positive breast cancer cells
Although breast cancer treatment has evolved significantly in recent years, drug resistance remains a major challenge. To identify new targets for breast cancer, we found that stage-specific embryonic antigen 4 (SSEA-4) is expressed in all subtypes of breast cancer cell lines, and the increased expression of the associated enzymes β3GalT5 and ST3Gal2 correlates with poor recurrence-free survival (RFS) in breast cancer. We also found that SSEA-4 antibodies can be rapidly internalized into breast cancer cells, a property that makes SSEA-4 an attractive target for antibody-drug conjugates (ADCs). Furthermore, the SSEA-4 antibody conjugated to the anticancer agents showed efficacy against SSEA-4-positive breast cancer cells, including those resistant to PARP inhibitor, trastuzumab, and CDK7 inhibitor. In addition, SSEA-4 ADCs showed no efficacy in β3GalT5-knockout MDA-MB-231 cells, highlighting the essential role of SSEA-4 as the target antigen for ADCs activity. Our work shows that SSEA-4-ADCs could be a therapeutic option for breast cancers.
Authors
- Kyung Ho Han (ORCID: https://orcid.org/0000-0001-6907-1462)
- Yu-Chieh Hsu
- Chih‐Wei Lin (ORCID: https://orcid.org/0000-0002-5836-7994)
- Yi‐Chuan Li (ORCID: https://orcid.org/0000-0002-1795-1051)
- Yuan‐Soon Ho (ORCID: https://orcid.org/0000-0002-3649-6680)
- Chi‐Huey Wong (ORCID: https://orcid.org/0000-0002-9961-7865)
- Muhammad Usama (ORCID: https://orcid.org/0000-0001-6593-7089)
- Mien‐Chie Hung (ORCID: https://orcid.org/0000-0003-4317-4740)
- Hirohito Yamaguchi (ORCID: https://orcid.org/0000-0003-0425-916X)
- Chung‐Yu Chen (ORCID: https://orcid.org/0000-0002-1725-0079)
- Mahdieh Safaei
Institutions
- Hannam University (KR)
- Scripps Research Institute (US)
- China Medical University (TW)
Publication Details
- Journal
- Cancer Letters
- Published
- 2025-01-09
- DOI
- https://doi.org/10.1016/j.canlet.2025.217453
- Citations
- 4
- Primary Topic
- Monoclonal and Polyclonal Antibodies Research
- Type
- article
- Field-Weighted Citation Impact
- 5.44