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J Clin Oncol. 2009 Nov 10;27(32):5459-68. doi: 10.1200/JCO.2009.22.1291. Epub 2009 Oct 13.
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Genome-wide analysis of survival in early-stage non-small-cell lung cancer.早期非小细胞肺癌生存情况的全基因组分析。
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Copy number alterations that predict metastatic capability of human breast cancer.预测人类乳腺癌转移能力的拷贝数改变。
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Translation of the Philadelphia chromosome into therapy for CML.将费城染色体转化为慢性粒细胞白血病的治疗方法。
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Comprehensive genomic characterization defines human glioblastoma genes and core pathways.全面的基因组特征分析确定了人类胶质母细胞瘤的基因和核心通路。
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Genome-wide copy number profiling reveals molecular evolution from diagnosis to relapse in childhood acute lymphoblastic leukemia.全基因组拷贝数分析揭示儿童急性淋巴细胞白血病从诊断到复发的分子演变。
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Genetic architecture of transcript-level variation in humans.人类转录水平变异的遗传结构
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8
A second generation human haplotype map of over 3.1 million SNPs.一张包含超过310万个单核苷酸多态性的第二代人类单倍型图谱。
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Gene expression profiling in breast cancer.乳腺癌中的基因表达谱分析
Curr Opin Oncol. 2007 Nov;19(6):547-51. doi: 10.1097/CCO.0b013e3282f0ada3.
10
UGT1A1*28 genotype and irinotecan-induced neutropenia: dose matters.UGT1A1*28基因分型与伊立替康诱导的中性粒细胞减少:剂量至关重要。
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肿瘤药理学基因组标志物发现方法:2000-2010-2020 年。

Approaches to the discovery of pharmacogenomic markers in oncology: 2000-2010-2020.

机构信息

Department of Medicine, University of Chicago, IL 60637, USA.

出版信息

Pharmacogenomics. 2010 Apr;11(4):471-4. doi: 10.2217/pgs.10.11.

DOI:10.2217/pgs.10.11
PMID:20350124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2864525/
Abstract

Pharmacogenomics is emerging as an important component both in facilitating new drug development and in improving the utility of existing chemotherapeutic agents. Both candidate gene and genome-wide approaches have been used to identify genetic markers associated with chemotherapeutic response and/or toxicity. New molecular targeted agents have been designed based on a sophisticated understanding of the molecular alterations defining cancers. Over the next decade, the translation of these findings into clinical practice, as well as functional studies of genetic variants, is likely to take center stage. More comprehensive evaluation of the human genome, including the examination of rare SNPs, copy number variations, tandem repeats and epigenetic effects, will further improve our understanding of the relationship between genetics and drug response.

摘要

药物基因组学正在成为新药开发和提高现有化疗药物疗效的重要组成部分。候选基因和全基因组方法都被用于识别与化疗反应和/或毒性相关的遗传标记。新的分子靶向药物是基于对定义癌症的分子改变的深入了解而设计的。在未来十年,这些发现转化为临床实践,以及对遗传变异的功能研究,可能将成为关注的焦点。更全面地评估人类基因组,包括检查罕见的单核苷酸多态性、拷贝数变异、串联重复和表观遗传效应,将进一步提高我们对遗传与药物反应之间关系的理解。