DNA repair and cell cycle checkpoint defects as drivers and therapeutic targets in melanoma. (5th August 2013)

• Record Type: Journal Article
• Authors: Pavey, Sandra; Spoerri, Loredana; Haass, Nikolas K.; Gabrielli, Brian
• Is Part Of: Pigment cell & melanoma research. Volume 26:Number 6(2013:Nov.)
• Page Start: 805
• Page End: 816
• Publication Date: 2013-08-05
• Subjects: UV -- DNA damage -- DNA repair -- cell cycle checkpoint; Melanoma -- Periodicals; Chromatophores -- Periodicals; Animal pigments -- Periodicals; 616.99477
• DOI: 10.1111/pcmr.12136
• Languages: English
• ISSNs: 1755-1471

Abstract

Summary: The ultraviolet radiation (UVR) component of sunlight is the major environmental risk factor for melanoma, producing DNA lesions that can be mutagenic if not repaired. The high level of mutations in melanomas that have the signature of UVR‐induced damage indicates that the normal mechanisms that detect and repair this damage must be defective in this system. With the exception of melanoma‐prone heritable syndromes which have mutations of repair genes, there is little evidence for somatic mutation of known repair genes. Cell cycle checkpoint controls are tightly associated with repair mechanisms, arresting cells to allow for repair before continuing through the cell cycle. Checkpoint signaling components also regulate the repair mechanisms. Defects in checkpoint mechanisms have been identified in melanomas and are likely to be responsible for increased mutation load in melanoma. Loss of the checkpoint responses may also provide an opportunity to target melanomas using a synthetic lethal approach to identify and inhibit mechanisms that compensate for the defective checkpoints.