Abstract 1738: Histone deacetylase inhibitor mediated reversal of acquired endocrine therapy resistance in breast cancer cell lines

Author(s):  
Paromita Raha ◽  
Scott Thomas ◽  
K Ted Thurn ◽  
Pamela Munster
2015 ◽  
Vol 55 (10) ◽  
pp. 1477-1485 ◽  
Author(s):  
Erika Contreras-Leal ◽  
Andrés Hernández-Oliveras ◽  
Lucía Flores-Peredo ◽  
Ángel Zarain-Herzberg ◽  
Juan Santiago-García

2021 ◽  
Vol 22 (16) ◽  
pp. 8573
Author(s):  
Marta Hałasa ◽  
Jarogniew J. Łuszczki ◽  
Magdalena Dmoszyńska-Graniczka ◽  
Marzena Baran ◽  
Estera Okoń ◽  
...  

Breast cancer (BC) is the leading cause of death in women all over the world. Currently, combined chemotherapy with two or more agents is considered a promising anti-cancer tool to achieve better therapeutic response and to reduce therapy-related side effects. In our study, we demonstrated an antagonistic effect of cytostatic agent-cisplatin (CDDP) and histone deacetylase inhibitor: cambinol (CAM) for breast cancer cell lines with different phenotypes: estrogen receptor positive (MCF7, T47D) and triple negative (MDA-MB-231, MDA-MB-468). The type of pharmacological interaction was assessed by an isobolographic analysis. Our results showed that both agents used separately induced cell apoptosis; however, applying them in combination ameliorated antiproliferative effect for all BC cell lines indicating antagonistic interaction. Cell cycle analysis showed that CAM abolished cell cycle arrest in S phase, which was induced by CDDP. Additionally, CAM increased cell proliferation compared to CDDP used alone. Our data indicate that CAM and CDDP used in combination produce antagonistic interaction, which could inhibit anti-cancer treatment efficacy, showing importance of preclinical testing.


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