Hypersensitivity to Aurora Kinase Inhibitors in Cells Resistant against Platinum- Containing Anticancer Agents
- 作者: Akiyama M.1, Izumi H.2, Wang K.3, Yamaguchi T.4, Kuma A.5, Kitamura N.6, Harada Y.7, Oya R.8, Yamaguchi K.9, Iwai Y.10, Kohno K.11
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- 期: 卷 14, 编号 7 (2014)
- 页面: 1042-1050
- 栏目: Oncology
- URL: https://kld-journal.fedlab.ru/1871-5206/article/view/695122
- DOI: https://doi.org/10.2174/1871520614666140207154351
- ID: 695122
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The aurora kinases are serine/threonine kinases that are essential for mitosis and contribute to tumorigenesis. Therefore, aurora kinases hold promise for molecularly targeted therapy. In the present study, we demonstrated that aurora B kinase (AURKB) is overexpressed in both cisplatin- and oxaliplatin-resistant cells. Downregulation of AURKB sensitized cells to both cisplatin and oxaliplatin, but not to paclitaxel, 5-FU or hydrogen peroxide. Interestingly, we found that both cisplatin- and oxaliplatin-resistant cells were hypersensitive to the AURKB specific inhibitors, AZD1152 HQPA and ZM447439, suggesting that both cisplatin- and oxaliplatinresistant cells develop an addiction to AURKB. These data provide evidence that aurora kinase inhibitors can overcome both cisplatin and oxaliplatin resistance. Therefore, AURKB inhibitors could offer potential benefits if used after first-line platinum-based chemotherapy.
作者简介
Masaki Akiyama
aff1
Email: info@benthamscience.net
Hiroto Izumi
aff2
Email: info@benthamscience.net
Ke-Yong Wang
aff3
Email: info@benthamscience.net
Takahiro Yamaguchi
aff4
Email: info@benthamscience.net
Akihiro Kuma
aff5
Email: info@benthamscience.net
Noriaki Kitamura
aff6
Email: info@benthamscience.net
Yoshikazu Harada
aff7
Email: info@benthamscience.net
Ryoichi Oya
aff8
Email: info@benthamscience.net
Koji Yamaguchi
aff9
Email: info@benthamscience.net
Yoshiko Iwai
aff10
Email: info@benthamscience.net
Kimitoshi Kohno
aff11
Email: info@benthamscience.net
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