Human Fibroblasts for Large-Scale "Omics" Investigations of ATM Gene Function

被引:8
|
作者
Jung, Mira [1 ]
Timofeeva, Olga [2 ]
Cheema, Amrita K. [2 ]
Varghese, Rency [2 ]
Ressom, Habtom [2 ]
Dritschilo, Anatoly [1 ,2 ,3 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Radiat Med, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[2] Georgetown Univ, Med Ctr, Dept Oncol, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
[3] Georgetown Univ, Med Ctr, Dept Radiat Med, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
关键词
ATAXIA-TELANGIECTASIA; RADIATION SENSITIVITY; KINASES; CELLS;
D O I
10.1007/978-1-4614-0254-1_15
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ATM (gene mutated in ataxia-telangiectasia) is a critical central component of the pleiotropic responses of cells to ionizing radiation-induced stress. To gain insight into molecular mechanisms and to enhance our understanding of ATM functions, we have advanced a human model cell system, derived from genetically defined immortal fibroblasts, and we have applied high-throughput genomic, proteomic and metabolomic technologies for a systems level analysis. The cellular characterizations reported here provide the background for application of a systems analysis to integrate transcription, post-translational modifications and metabolic activity induced by exposure of cells to ionizing radiation. We present here a summary of the derivation and characterization of cells comprising this model cell system and review applications of this model to systems analysis of ATM functions.
引用
收藏
页码:181 / 190
页数:10
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