The DOI matches its Crossref record; 129 of the 129 references it cites were found in a registry or an index.
Aurora kinases: novel therapy targets in cancers
Open accessAbstract
// Anqun Tang 1,* , Keyu Gao 1,* , Laili Chu 1,* , Rui Zhang 1 , Jing Yang 1 and Junnian Zheng 1,2 1 Jiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Cancer Institute, Jiangsu, China 2 Department of Oncology, The First Affiliated Hospital, Xuzhou Medical University, Xuzhou, Jiangsu, China * These authors have contributed equally to this work Correspondence to: Junnian Zheng, email: // Jing Yang, email: // Keywords : Aurora kinases, mitosis, cancer therapy target, Aurora kinases inhibitors, combination therapy Received : November 01, 2016 Accepted : January 17, 2017 Published : January 29, 2017 Abstract Aurora kinases, a family of serine/threonine kinases, consisting of Aurora A (AURKA), Aurora B (AURKB) and Aurora C (AURKC), are essential kinases for cell division via regulating mitosis especially the process of chromosomal segregation. Besides regulating mitosis, Aurora kinases have been implicated in regulating meiosis. The deletion of Aurora kinases could lead to failure of cell division and impair the embryonic development. Overexpression or gene amplification of Aurora kinases has been clarified in a number of cancers. And a growing number of studies have demonstrated that inhibition of Aurora kinases could potentiate the effect of chemotherapies. For the past decades, a series of Aurora kinases inhibitors (AKIs) developed effectively repress the progression and growth of many cancers both in vivo and in vitro , suggesting that Aurora kinases could be a novel therapeutic target. In this review, we’ll first briefly present the structure, localization and physiological functions of Aurora kinases in mitosis, then describe the oncogenic role of Aurora kinases in tumorigenesis, we shall finally discuss the outcomes of AKIs combination with conventional therapy.
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1 retracted
BRCA1 Phosphorylation by Aurora-A in the Regulation of G2 to M Transition
Ouchi, M., Fujiuchi, N., Sasai, K., Katayama, H., Minamishima, Y. A., Ongusaha, P. P., Deng, C., Sen, S., Lee, S. W., & Ouchi, T. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m311780200 · Cited by 199
RetractedOverriding Imatinib Resistance with a Novel ABL Kinase Inhibitor
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Mitotic kinases as regulators of cell division and its checkpoints
Nigg, E. A. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35048096 · Cited by 1,547
A homologue of Drosophila aurora kinase is oncogenic and amplified in human colorectal cancers
Bischoff, J. R. (1998) · The EMBO Journal · doi:10.1093/emboj/17.11.3052 · Cited by 1,216
Wnt signaling in disease and in development
NUSSE, R. (2005) · Cell Research · doi:10.1038/sj.cr.7290260 · Cited by 973
The chromosomal passenger complex (CPC): from easy rider to the godfather of mitosis
Carmena, M., Wheelock, M., Funabiki, H., & Earnshaw, W. C. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3474 · Cited by 905
Roles of Aurora Kinases in Mitosis and Tumorigenesis
Fu, J., Bian, M., Jiang, Q., & Zhang, C. (2007) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-06-0208 · Cited by 614
Phosphorylation by aurora kinase A induces Mdm2-mediated destabilization and inhibition of p53
Katayama, H., Sasai, K., Kawai, H., Yuan, Z.-M., Bondaruk, J., Suzuki, F., Fujii, S., Arlinghaus, R. B., Czerniak, B. A., & Sen, S. (2004) · Nature Genetics · doi:10.1038/ng1279 · Cited by 588
Human TPX2 is required for targeting Aurora-A kinase to the spindle
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Exploring the Functional Interactions between Aurora B, INCENP, and Survivin in Mitosis
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Dugourd, A., Kuppe, C., Sciacovelli, M., Gjerga, E., Gabor, A., Emdal, K. B., Vieira, V., Bekker‐Jensen, D. B., Kranz, J., Bindels, E. M. J., et al. (2021) · Molecular Systems Biology · doi:10.15252/msb.20209730 · Cited by 149
Blazejewski, S. M., Bennison, S. A., Liu, X., & Toyo-oka, K. (2021) · Scientific Reports · doi:10.1038/s41598-021-87521-3 · Cited by 27
Metadata
- Authors
- Tang, A., Gao, K., Chu, L., Zhang, R., Yang, J., & Zheng, J.
- Venue
- Oncotarget
- Publisher
- Impact Journals, LLC
- Published
- 2017-01-29
- Volume
- 8
- Issue
- 14
- Pages
- 23937-23954
- ISSN
- 1949-2553 (ISSN-L)
- OpenAlex
- W2585352231
- Cited by
- 382
- References
- 129
- FWCI
- 16.23
- Type
- journal article
- Language
- en
- Open access
- diamond
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