Literature DB >> 17209521

Therapeutic potential of Aurora kinase inhibitors in cancer.

Krishna S Naruganahalli1, Manikandan Lakshmanan, Sunanda G Dastidar, Abhijit Ray.   

Abstract

Aurora kinases (AKs) represent a family of serine/threonine protein kinases that regulate mitotic processes during cell division. They are primarily involved in regulating the multiple steps of mitosis, including centrosome duplication, formation of bipolar mitotic spindle, chromosome alignment on the mitotic spindle, establishment and maintenance of the spindle checkpoint and cytokinesis. As AKs are key regulators of mitosis, several studies have indicated that they have a strong association with cancer and are overexpressed in numerous cancerous cell lines as well as human malignancies. Thus, AKs represent a promising therapeutic target for anticancer drug development. In this review, the role of AKs in cancer, and the current status and therapeutic potential of AK inhibitors is discussed.

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Year:  2006        PMID: 17209521

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  10 in total

1.  The induction of polyploidy or apoptosis by the Aurora A kinase inhibitor MK8745 is p53-dependent.

Authors:  Jayasree S Nair; Alan L Ho; Gary K Schwartz
Journal:  Cell Cycle       Date:  2012-02-15       Impact factor: 4.534

2.  Uncovering new substrates for Aurora A kinase.

Authors:  Teresa Sardon; Roland A Pache; Amelie Stein; Henrik Molina; Isabelle Vernos; Patrick Aloy
Journal:  EMBO Rep       Date:  2010-11-12       Impact factor: 8.807

3.  MK615 inhibits pancreatic cancer cell growth by dual inhibition of Aurora A and B kinases.

Authors:  Toshie Okada; Tokihiko Sawada; Tatsushi Osawa; Masakazu Adachi; Keiichi Kubota
Journal:  World J Gastroenterol       Date:  2008-03-07       Impact factor: 5.742

4.  Advanced malignant melanoma responds to Prunus mume Sieb. Et Zucc (Ume) extract: Case report and in vitro study.

Authors:  Shigeto Matsushita; Ko-Ichi Tada; Ko-Ichi Kawahara; Kazuhiro Kawai; Teruto Hashiguchi; Ikuro Maruyama; Takuro Kanekura
Journal:  Exp Ther Med       Date:  2010-07-01       Impact factor: 2.447

5.  Effects of stable knockdown of Aurora kinase A on proliferation, migration, chromosomal instability, and expression of focal adhesion kinase and matrix metalloproteinase-2 in HEp-2 cells.

Authors:  Hao Zhang; Xuehua Chen; Bingya Liu; Liang Zhou
Journal:  Mol Cell Biochem       Date:  2011-05-18       Impact factor: 3.396

6.  AURKA promotes cell migration and invasion of head and neck squamous cell carcinoma through regulation of the AURKA/Akt/FAK signaling pathway.

Authors:  Jichang Wu; Liyun Yang; Yamin Shan; Changping Cai; Shili Wang; Hao Zhang
Journal:  Oncol Lett       Date:  2016-01-14       Impact factor: 2.967

7.  Hainanerectamines A-C, alkaloids from the Hainan sponge Hyrtios erecta.

Authors:  Wen-Fei He; Duo-Qing Xue; Li-Gong Yao; Jing-Ya Li; Jia Li; Yue-Wei Guo
Journal:  Mar Drugs       Date:  2014-06-30       Impact factor: 5.118

8.  A Vector-Based Short Hairpin RNA Targeting Aurora B Suppresses Human Prostatic Carcinoma Growth.

Authors:  Mei Cao; Panpan Qi; Chong Chen; Liju Song; Xuege Wang; Ningzhe Li; Daoyan Wu; Guoku Hu; Jian Zhao
Journal:  Technol Cancer Res Treat       Date:  2016-10-17

9.  Enhanced Cytotoxic Effects of Combined Valproic Acid and the Aurora Kinase Inhibitor VE465 on Gynecologic Cancer Cells.

Authors:  Yanfang Li; Tao Liu; Cristina Ivan; Jie Huang; De-Yu Shen; John J Kavanagh; Robert C Bast; Siqing Fu; Wei Hu; Anil K Sood
Journal:  Front Oncol       Date:  2013-03-20       Impact factor: 6.244

10.  Insights into p53 transcriptional function via genome-wide chromatin occupancy and gene expression analysis.

Authors:  F Nikulenkov; C Spinnler; H Li; C Tonelli; Y Shi; M Turunen; T Kivioja; I Ignatiev; A Kel; J Taipale; G Selivanova
Journal:  Cell Death Differ       Date:  2012-07-13       Impact factor: 15.828

  10 in total

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