4.6 Review

Chromosomal translocations in cancer

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER
Volume 1786, Issue 2, Pages 139-152

Publisher

ELSEVIER
DOI: 10.1016/j.bbcan.2008.07.005

Keywords

Leukemia; Lymphoma; Neoplasia; DNA repair; Double-strand break; Carcinoma; Sarcoma; Genomic instability; V(D)J recombination

Funding

  1. Lady Tata Memorial Trust, UK [TLCS/0520]
  2. DBT, India [BT/PRS129/GBD/27/7/2006]
  3. IISc
  4. CSIR, India

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Genetic alterations in DNA can lead to cancer when it is present in proto-oncogenes, tumor suppressor genes, DNA repair genes etc. Examples of such alterations include deletions, inversions and chromosomal translocations. Among these rearrangements chromosomal translocations are considered as the primary cause for many cancers including lymphoma, leukemia and some solid tumors. Chromosomal translocations in certain cases can result either in the fusion of genes or in bringing genes close to enhancer or promoter elements, hence leading to their altered expression. Moreover, chromosomal trainslocations are used as diagnostic markers for cancer and its therapeutics. In the first part of this review, we summarize the well-studied chromosomal translocations in cancer. Although the mechanism of formation of most of these translocations is still unclear, in the second part we discuss the recent advances in this area of research. (C) 2008 Elsevier B.V. All rights reserved.

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