DNA repair pathways and their therapeutic potential in lung cancer

被引:10
作者
Burgess, Joshua T. [1 ]
Croft, Laura V. [1 ]
Wallace, Nathan C. [1 ]
Stephenson, Sally-Anne [2 ]
Adams, Mark N. [1 ]
Ashton, Nicholas W. [1 ]
Solomon, Benjamin [3 ]
O'Byrne, Ken [1 ]
Richard, Derek J. [1 ]
机构
[1] Queensland Univ Technol, Inst Hlth Biomed Innovat, Translat Res Inst, Canc & Ageing Res Program,Genome Stabil Lab, Woolloongabba, Qld 4102, Australia
[2] Queensland Univ Technol, Inst Hlth Biomed Innovat, Translat Res Inst, Eph Receptor Biol Grp, Woolloongabba, Qld 4102, Australia
[3] Peter MacCallum Canc Ctr, Dept Med Oncol, Melbourne, Vic 3002, Australia
关键词
DNA damage repair; drug resistance; genetic mutations; lung cancer; synthetic lethality;
D O I
10.2217/LMT.14.12
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Lung cancer is the leading cause of cancer-related mortality. According to WHO, 1.37 million deaths occur globally each year as a result of this disease. More than 70% of these cases are associated with prior tobacco consumption and/or cigarette smoking, suggesting a direct causal relationship. The development and progression of lung cancer and other malignancies involves the loss of genetic stability, resulting in acquisition of cumulative genetic changes; this affords the cell increased malignant potential. As such, an understanding of the mechanisms through which these events may occur will potentially allow for development of new anticancer therapies. This review will address the association between lung cancer and genetic instability, with a central focus on genetic mutations in the DNA damage repair pathways. In addition, we will discuss the potential clinical exploitation of these pathways, both in terms of biomarker staging, as well as through direct therapeutic targeting.
引用
收藏
页码:159 / 173
页数:15
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