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Chromosome 20q Amplification Regulatesin VitroResponse to Kinesin-5 Inhibitor
Author(s) -
Aimee L. Jackson,
Mao Mao,
Sumire Kobayashi,
Teresa Ward,
Matthew C. Biery,
Hongyue Dai,
Steven R. Bartz,
Peter S. Linsley
Publication year - 2008
Publication title -
cancer informatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.606
H-Index - 31
ISSN - 1176-9351
DOI - 10.4137/cin.s609
Subject(s) - kinesin , gene , biology , chromosome , cancer research , genetics , microtubule
We identified gene expression signatures predicting responsiveness to a Kinesin-5 (KIF11) inhibitor (Kinesin-5i) in cultured colon tumor cell lines. Genes predicting resistance to Kinesin-5i were enriched for those from chromosome 20q, a region of frequent amplification in a number of tumor types. siRNAs targeting genes in this chromosomal region identified AURKA, TPX2 and MYBL2 as genes whose disruption enhances response to Kinesin-5i. Taken together, our results show functional interaction between these genes, and suggest that their overexpression is involved in resistance to Kinesin-5i. Furthermore, our results suggest that patients whose tumors overexpress AURKA due to amplification of 20q will more likely resist treatment with Kinesin-5 inhibitor, and that inactivation of AURKA may sensitize these patients to treatment.

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