精密医学
个性化医疗
药物开发
临床试验
癌症
医学
药物发现
计算生物学
药品
生物信息学
肿瘤科
生物
内科学
药理学
病理
作者
Sung‐Yup Cho,Wonyoung Kang,Jee Yun Han,Seoyeon Min,Jinjoo Kang,Ahra Lee,Jee Young Kwon,Charles Lee,Hansoo Park
出处
期刊:Molecules and Cells
[Springer Science+Business Media]
日期:2016-02-01
卷期号:39 (2): 77-86
被引量:151
标识
DOI:10.14348/molcells.2016.2350
摘要
Cancer is a heterogeneous disease caused by diverse genomic alterations in oncogenes and tumor suppressor genes. Despite recent advances in high-throughput sequencing technologies and development of targeted therapies, novel cancer drug development is limited due to the high attrition rate from clinical studies. Patient-derived xenografts (PDX), which are established by the transfer of patient tumors into immunodeficient mice, serve as a platform for co-clinical trials by enabling the integration of clinical data, genomic profiles, and drug responsiveness data to determine precisely targeted therapies. PDX models retain many of the key characteristics of patients' tumors including histology, genomic signature, cellular heterogeneity, and drug responsiveness. These models can also be applied to the development of biomarkers for drug responsiveness and personalized drug selection. This review summarizes our current knowledge of this field, including methodologic aspects, applications in drug development, challenges and limitations, and utilization for precision cancer medicine.
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