MicroRNA Gene Dosage Alterations and Drug Response in Lung Cancer

被引:15
作者
Enfield, Katey S. S. [1 ]
Stewart, Greg L. [1 ]
Pikor, Larissa A. [1 ]
Alvarez, Carlos E. [2 ]
Lam, Stephen [1 ]
Lam, Wan L. [1 ]
Chari, Raj [1 ]
机构
[1] British Columbia Canc Res Ctr, Vancouver, BC V5Z 1L3, Canada
[2] Nationwide Childrens Hosp, Res Inst, Columbus, OH 43205 USA
来源
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY | 2011年
基金
美国国家卫生研究院;
关键词
EXPRESSION ANALYSIS; DOWN-REGULATION; TUMOR-CELLS; DNA-REPAIR; IDENTIFICATION; RESISTANCE; METASTASIS; ANTICANCER; PACLITAXEL; GEFITINIB;
D O I
10.1155/2011/474632
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Chemotherapy resistance is a key contributor to the dismal prognoses for lung cancer patients. While the majority of studies have focused on sequence mutations and expression changes in protein-coding genes, recent reports have suggested that microRNA ( miRNA) expression changes also play an influential role in chemotherapy response. However, the role of genetic alterations at miRNA loci in the context of chemotherapy response has yet to be investigated. In this study, we demonstrate the application of an integrative, multidimensional approach in order to identify miRNAs that are associated with chemotherapeutic resistance and sensitivity utilizing publicly available drug response, miRNA loci copy number, miRNA expression, and mRNA expression data from independent resources. By instigating a logical stepwise strategy, we have identified specific miRNAs that are associated with resistance to several chemotherapeutic agents and provide a proof of principle demonstration of how these various databases may be exploited to derive relevant pharmacogenomic results.
引用
收藏
页数:15
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