Common Fragile Sites: Genomic Hotspots of DNA Damage and Carcinogenesis

International Journal of Molecular Sciences

Ke Ma²  Li Qiu²  Kristin Mrasek¹  Jun Zhang²  Thomas Liehr¹  Luciana Gon๺lves Quintana¹ 

[1] Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, D-07743 Jena, Germany; E-Mails:;Department of Biochemistry and Molecular Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China; E-Mails:

关键词: replication;    instability;    CFS;    cancer;    FATS;    checkpoint;   

DOI  :  10.3390/ijms130911974

来源: mdpi

【 摘 要 】

Genomic instability, a hallmark of cancer, occurs preferentially at specific genomic regions known as common fragile sites (CFSs). CFSs are evolutionarily conserved and late replicating regions with AT-rich sequences, and CFS instability is correlated with cancer. In the last decade, much progress has been made toward understanding the mechanisms of chromosomal instability at CFSs. However, despite tremendous efforts, identifying a cancer-associated CFS gene (CACG) remains a challenge and little is known about the function of CACGs at most CFS loci. Recent studies of FATS (for Fragile-site Associated Tumor Suppressor), a new CACG at FRA10F, reveal an active role of this CACG in regulating DNA damage checkpoints and suppressing tumorigenesis. The identification of FATS may inspire more discoveries of other uncharacterized CACGs. Further elucidation of the biological functions and clinical significance of CACGs may be exploited for cancer biomarkers and therapeutic benefits.

【 授权许可】

CC BY   
© 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland.