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Hyunki Kim1, Sharon L Samuel2, Guihua Zhai2
1Department of Radiology; University of Alabama at Birmingham; Birmingham, AL USA; Department of Biomedical Engineering; University of Alabama at Birmingham; Birmingham, AL USA; Comprehensive Cancer Center; University of Alabama at Birmingham; Birmingham, AL USA.
Abstract:
TRA-8, a monoclonal antibody targeting death receptor, has demonstrated high therapeutic effect for triple negative breast cancer (TNBC) in preclinical models. Tamoxifen, the standard of care for ERα-positive breast cancer, induces apoptosis via ERβ, which commonly presents in TNBC cells. The current study investigates the combination effects of TRA-8 and tamoxifen for TNBC. In vitro assays were implemented with two ERβ-positive TNBC cell lines, SUM159 and 2LMP, and in vivo therapy studies were followed using orthotopic breast tumor mouse models. IC50 of tamoxifen for SUM159 and 2LMP were 29 μM and 38 μM, respectively. Synergy between TRA-8 (0-1000 ng/mL) and tamoxifen (20 μM) was observed for both the cell lines. Tamoxifen (400 mg/kg diet) markedly suppressed the growth of SUM159 tumors for 6 weeks after therapy initiation, but it did not induce antitumor effect for 2LMP tumors. TRA-8 (0.1 mg, weekly, i.p.) successfully arrested the growth of both SUM159 and 2LMP tumors during therapy, but an antagonistic effect was observed when tamoxifen was combined. TRA-8 uptake into tumors was not changed by tamoxifen treatment. Histological analysis confirmed that caspase-3 activation induced by TRA-8 was significantly decreased when tamoxifen was used in combination. In conclusion, our findings suggest that the combined use of TRA-8 and tamoxifen may cause antagonistic effects for TNBC patients.
Insights
Combining TRA-8 antibody and tamoxifen showed antagonistic effects in triple-negative breast cancer (TNBC) models. While TRA-8 alone arrested tumor growth, its combination with tamoxifen decreased therapeutic efficacy and caspase-3 activation in TNBC.
Area of Science:
- Oncology
- Immunotherapy
- Pharmacology
Background:
- Triple-negative breast cancer (TNBC) lacks targeted therapies.
- TRA-8, a death receptor antibody, shows promise for TNBC.
- Tamoxifen, used for ERα-positive breast cancer, targets ERβ, often found in TNBC.
Purpose of the Study:
- To investigate the combined therapeutic effects of TRA-8 and tamoxifen in TNBC.
- To evaluate the efficacy of this combination in preclinical TNBC models.
Main Methods:
- In vitro studies using ERβ-positive TNBC cell lines (SUM159, 2LMP).
- In vivo studies using orthotopic breast tumor mouse models.
- Assessed synergy, tumor growth suppression, antibody uptake, and caspase-3 activation.
Main Results:
- TRA-8 and tamoxifen showed in vitro synergy against TNBC cell lines.
- Tamoxifen suppressed SUM159 tumors but not 2LMP tumors.
- TRA-8 alone arrested tumor growth, but combination therapy showed antagonism.
- Combined treatment reduced TRA-8 uptake and decreased TRA-8-induced caspase-3 activation.
Conclusions:
- The combination of TRA-8 and tamoxifen may have antagonistic effects in TNBC.
- This combination could reduce the therapeutic efficacy of TRA-8 in TNBC patients.
- Further research is needed to understand the mechanisms behind this antagonism.
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