DNA repair pathways and their therapeutic potential in lung cancer

Author:

Burgess Joshua T1,Croft Laura V1,Wallace Nathan C1,Stephenson Sally-Anne2,Adams Mark N1,Ashton Nicholas W1,Solomon Benjamin3,O’Byrne Ken1,Richard Derek J1

Affiliation:

1. Genome Stability Laboratory, Cancer & Ageing Research Program, Institute of Health & Biomedical Innovation, Translational Research Institute, Queensland University of Technology, Woolloongabba, Queensland 4102, Australia

2. Eph Receptor Biology Group, Institute of Health & Biomedical Innovation, Translational Research Institute, Queensland University of Technology, Woolloongabba, Queensland 4102, Australia

3. Department of Medical Oncology, Peter MacCallum Cancer Centre, East Melbourne 3002, Australia

Abstract

SUMMARY:  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.

Publisher

Future Medicine Ltd

Subject

Pulmonary and Respiratory Medicine,Oncology

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