Oncogenic chromosomal translocations and human cancer (review).

Abstract:

:Chromosomal translocations are very common in human cancer. The molecular mechanisms of chromosomal translocations are complex and are not fully understood. Recent studies showed organization of genomes is higher-order in the nucleus and every chromosome or chromatin has its preferential position and territory. These findings suggest the spatial arrangements of chromosomes and gene loci in the interphase nucleus are responsible for non-random chromosomal translocations in human cancer. Chromosomal translocations are favored in neighboring chromosomes or genes in spatial proximity within the nucleus. Chromosomal translocations leading to cancer are generally via two ways, formation of oncogenic fusion protein or oncogene activation by a new promoter or enhancer. This review focuses mainly on the recent advances in oncogenic chromosomal translocations in human cancer.

journal_name

Oncol Rep

journal_title

Oncology reports

authors

Zheng J

doi

10.3892/or.2013.2677

subject

Has Abstract

pub_date

2013-11-01 00:00:00

pages

2011-9

issue

5

eissn

1021-335X

issn

1791-2431

journal_volume

30

pub_type

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