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Effectiveness of Rhenium(I)-diselenoether Low Doses in a Triple-negative Breast Cancer Chicken Embryo Model
Philippe Collery1, Chloe Prunier2, Emilien Dosda2
1Société de Coordination de Recherches Thérapeutiques, Algajola, France; philippe.collery@gmail.com.
Anticancer Research
|February 29, 2024
Summary
Rhenium(I)-diselenoether (Re-diSe) shows anticancer effects, with a low dose (0.1 mg/kg) reducing tumor weight. A higher dose (10 mg/kg) eliminated tumors, possibly via immune responses, confirming Re-diSe as an effective anticancer agent.
Area of Science:
- Oncology
- Materials Science
- Pharmacology
Background:
- Rhenium(I)-diselenoether (Re-diSe) is a novel anticancer agent.
- Previous studies showed Re-diSe inhibited cancer cells and tumors, but with conflicting results in different models.
- This study aimed to validate Re-diSe efficacy in a specific breast cancer model.
Purpose of the Study:
- To evaluate the anticancer efficacy of Re-diSe in a transplanted MDA-MB-231 breast tumor model using the chicken chorioallantoic membrane (CAM) assay.
- To investigate dose-dependent effects of Re-diSe on tumor growth and characteristics.
- To clarify discrepancies in Re-diSe's anti-tumor activity observed in previous studies.
Main Methods:
- MDA-MB-231 cancer cells were xenografted onto chicken chorioallantoic membranes.
- Daily administration of Re-diSe at 0.1, 1, and 10 mg/kg for nine days.
- Tumor weight, histological analysis, and inflammatory cell infiltration were assessed.
Main Results:
- A low dose of 0.1 mg/kg significantly reduced tumor weights.
- The 1 mg/kg dose increased inflammation but did not significantly alter tumor weight compared to the 0.1 mg/kg dose.
- The 10 mg/kg dose eliminated visible tumors in 6/11 embryos, showing extensive necrosis and inflammatory cell infiltration.
Conclusions:
- Re-diSe demonstrated anticancer efficacy at a low dose (0.1 mg/kg) in this model.
- The higher dose (10 mg/kg) may exert anti-tumor effects through immune-mediated mechanisms.
- Re-diSe is confirmed as an effective anticancer agent with potential for further development.

