Literature DB >> 10341705

Perspective: chromosomal translocations can affect genes controlling gene expression and differentiation--why are these functions targeted?

T H Rabbitts1.   

Abstract

Chromosomal translocations are important aetiological factors in many human cancers. These aberrant chromosomes cause enforced expression of oncogenes located near the breakpoints or results in tumour-specific fusion proteins. Among the characteristics which influence the tumourigenic effect, it is observed that the genes at translocation junctions are often transcription factors and often normally involved in developmental processes. Furthermore, protein-protein interactions are key elements in the mechanism by which the translocation gene products exert their pathogenic effects. In this review some of these salient features are discussed and generalizations are suggested which may be applicable to the influence of chromosomal translocations on acute forms of cancer.

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Year:  1999        PMID: 10341705     DOI: 10.1002/(SICI)1096-9896(199901)187:1<39::AID-PATH235>3.0.CO;2-Q

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  7 in total

1.  Aberrant ALK tyrosine kinase signaling. Different cellular lineages, common oncogenic mechanisms.

Authors:  M Ladanyi
Journal:  Am J Pathol       Date:  2000-08       Impact factor: 4.307

2.  mSin3A regulates murine erythroleukemia cell differentiation through association with the TAL1 (or SCL) transcription factor.

Authors:  S Huang; S J Brandt
Journal:  Mol Cell Biol       Date:  2000-03       Impact factor: 4.272

3.  Gene targeting reveals a crucial role for MTG8 in the gut.

Authors:  F Calabi; R Pannell; G Pavloska
Journal:  Mol Cell Biol       Date:  2001-08       Impact factor: 4.272

Review 4.  Molecular genetics of pediatric soft tissue tumors: clinical application.

Authors:  Chung-Che Chang; Vinod B Shidham
Journal:  J Mol Diagn       Date:  2003-08       Impact factor: 5.568

5.  The EWS-Oct-4 fusion gene encodes a transforming gene.

Authors:  Jungwoon Lee; Ja Young Kim; In Young Kang; Hye Kyoung Kim; Yong-Mahn Han; Jungho Kim
Journal:  Biochem J       Date:  2007-09-15       Impact factor: 3.857

6.  Gene amplification and associated loss of 5' regulatory sequences of CoAA in human cancers.

Authors:  Y Sui; Z Yang; S Xiong; L Zhang; K L Blanchard; S C Peiper; W S Dynan; D Tuan; L Ko
Journal:  Oncogene       Date:  2006-07-31       Impact factor: 8.756

7.  EWS-Oct-4B, an alternative EWS-Oct-4 fusion gene, is a potent oncogene linked to human epithelial tumours.

Authors:  S Kim; B Lim; J Kim
Journal:  Br J Cancer       Date:  2010-01-05       Impact factor: 7.640

  7 in total

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