scholarly journals Antagonistic Interaction between Histone Deacetylase Inhibitor: Cambinol and Cisplatin—An Isobolographic Analysis in Breast Cancer In Vitro Models

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.

2021 ◽  
Author(s):  
Yukiko Hazama ◽  
Takayuki Tsujioka ◽  
Arisu Sakamoto ◽  
Yuka Miyaji ◽  
Akira Kitanaka ◽  
...  

Abstract The prognosis of the patients with inoperable or advanced granulosa cell tumors (GCTs) is still poor, and therefore it is important to establish a novel treatment strategy. Here we investigated the in vitro effects of a histone deacetylase inhibitor, panobinostat (PS) on two GCT cell lines (KGN and COV434). GCT cell lines were found to be susceptible to PS treatment and it inhibited cell growth mainly by apoptosis. In cell cycle analysis, PS reduced only the ratio of S phase in GCT cell lines. Combined treatment of PS with a deubiquitinases inhibitor, VLX1570 exerted an additive anti-proliferative effect on KGN and COV434. The gene set enrichment analysis revealed that PS treatment suppressed DNA replication- or cell cycle-related gene expression which led to chemotherapeutic cell death and in addition, this treatment induced activation of the gene set of adherens junction towards a normalized direction as well as activation of neuron-related gene sets that might imply unexpected differentiation potential due to epigenetic modification by a HDAC inhibitor in KGN cells. In the present study, we indicate a basis of a novel therapeutic availability of a HDAC inhibitor for the treatment of GCTs and further investigations will be warranted.


2006 ◽  
Vol 237 (1) ◽  
pp. 143-154 ◽  
Author(s):  
Ji Kon Ryu ◽  
Woo Jin Lee ◽  
Kwang Hyuck Lee ◽  
Jin-Hyeok Hwang ◽  
Yong-Tae Kim ◽  
...  

RSC Advances ◽  
2021 ◽  
Vol 11 (55) ◽  
pp. 34963-34978
Author(s):  
Başak Aru ◽  
Aysel Günay ◽  
Gülderen Yanıkkaya Demirel ◽  
Ayşe Gül Gürek ◽  
Devrim Atilla

3-Hydroxypyridin-2-thione bearing zinc and indium phthalocyanine derivatives, as photosensitizer agents have been synthesized and evaluated for their anti-cancer efficacy on two breast cancer cell lines, MDA-MB-231 and MCF-7 as well as a human endothelial cell line, HUVEC.


Sign in / Sign up

Export Citation Format

Share Document