Sequence and structural basis for chromosomal fragility during translocations in cancer. (September 2012)

• Record Type: Journal Article
• Authors: Gopalakrishnan, Vidya; Raghavan, Sathees C
• Is Part Of: Future oncology. Volume 8:Number 9(2012)
• Page Start: 1121
• Page End: 1134
• Publication Date: 2012-09
• Subjects: chromosomal abnormality -- DNA damage -- double-strand break -- genomic instability -- nonhomologous DNA end joining; Oncology -- Periodicals; 616.99405
• DOI: 10.2217/fon.12.107
• Languages: English
• ISSNs: 1479-6694

Abstract

Chromosomal aberration is considered to be one of the major characteristic features in many cancers. Chromosomal translocation, one type of genomic abnormality, can lead to deregulation of critical genes involved in regulating important physiological functions such as cell proliferation and DNA repair. Although chromosomal translocations were thought to be random events, recent findings suggest that certain regions in the human genome are more susceptible to breakage than others. The possibility of deviation from the usual B-DNA conformation in such fragile regions has been an active area of investigation. This review summarizes the factors that contribute towards the fragility of these regions in the chromosomes, such as DNA sequences and the role of different forms of DNA structures. Proteins responsible for chromosomal fragility, and their mechanism of action are also discussed. The effect of positioning of chromosomes within the nucleus favoring chromosomal translocations and the role of repair mechanisms are also addressed.