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DHPAC, a novel synthetic microtubule destabilizing agent, possess high anti-tumor activity in vincristine-resistant oral epidermoid carcinoma in vitro and in vivo

Author:
Zhang, Ying, Gong, Fu-Lian, Lu, Zhen-Ning, Wang, Hong-Yuan, Cheng, Yan-Na, Liu, Zhao-Peng, Yu, Lu-Gang, Zhang, Hui-Hui, Guo, Xiu-Li
Source:
The international journal of biochemistry & cell biology 2017 v.93 pp. 1-11
ISSN:
1357-2725
Subject:
antineoplastic activity, apoptosis, carcinoma, caspase-9, cell growth, colchicine, cyclins, cytochrome c, drug therapy, humans, inhibitory concentration 50, membrane potential, mice, microtubules, mitochondrial membrane, multiple drug resistance, phosphorylation
Abstract:
Multidrug resistance (MDR) is one of major obstacles to effective chemotherapeutic treatment of cancer. This study showed that DHPAC, 2-(6-ethoxy-3-(3-ethoxyphenylamino) −1-methyl-1,4-dihydroindeno[1,2-c]pyrazol-7-yloxy) acetamide, a novel compound that binds to the same site on microtubules as colchicine, has high anti-tumour activity in vincristine-resistant oral epidermoid carcinoma (KB/V) cells. It found that the presence of DHPAC strongly inhibited KB/V cell growth in vivo and in mice xenograft. The inhibitory effect of DHPAC is much stronger than that by colchicine in these KB/V cells (IC50: 64.4nM and 458.0nM respectively). Treatment of the cells with DHPAC induced cell apoptosis by reducing mitochondrial membrane potential and altered the expression of several apoptosis-related proteins such as Bcl-2, Bax, Caspase-9, Cytochrome c and PARP. DHPAC treatment also caused cell rest in G2/M phase by regulating of the expression of a number of cell cycle-related proteins (e.g. Cyclin B1, Cdc2, Cdc25b, Cdc25c, RSK2). Furthermore, DHPAC presence inhibits PTEN phosphorylation and PTEN/Akt/NF-κB signalling. Thus, DHPAC has potent anti-cancer activity in MDR tumuors and may be a potential therapeutic agent for the treatment of vincristine-resistant human oral epidermoid carcinoma.
Agid:
5848966