Skip Navigation


Carcinogenesis Advance Access originally published online on May 13, 2004
Carcinogenesis 2004 25(10):1795-1803; doi:10.1093/carcin/bgh187
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
25/10/1795    most recent
bgh187v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (6)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Velangi, M. R.
Right arrow Articles by Irving, J. A.E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Velangi, M. R.
Right arrow Articles by Irving, J. A.E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Carcinogenesis vol.25 no.10 © Oxford University Press 2004; all rights reserved.

ARTICLE

DNA mismatch repair pathway defects in the pathogenesis and evolution of myeloma

Mark R. Velangi3, Elizabeth C. Matheson, Gareth J. Morgan1, Graham H. Jackson2, Penelope R. Taylor2, Andrew G. Hall and Julie A.E. Irving

Northern Institute for Cancer Research, University of Newcastle upon Tyne, UK, 1 Department of Haematology, Leeds General Infirmary, Leeds, UK and 2 Department of Haematology, Royal Victoria Infirmary, Newcastle upon Tyne, UK

3 To whom correspondence should be addressed Email: ms.velangi{at}btinternet.com

Genetic instability is a prominent feature in multiple myeloma and progression of this disease from monoclonal gammopathy of uncertain significance (MGUS) and smouldering myeloma (SMM) is associated with increasing molecular and chromosomal abnormalities. The DNA mismatch repair (MMR) pathway is a post-replicational DNA repair system that maintains genetic stability by repairing mismatched bases and insertion/deletion loops mistakenly incorporated during DNA replication. Deficiencies in proteins pivotal to this pathway result in a higher mutation rate, particularly at regions of microsatellite DNA. We have investigated the proficiency of the MMR pathway in clinical samples and myeloma cell lines. Microsatellite analysis showed instability at one or more of nine loci examined in 15 from 92 patients: 7.7% of MGUS/SMM, 20.7% of MM/plasma cell leukaemia (PCL) and 12.5% of relapsed MM/PCL. An in vitro heteroduplex G/T repair assay found reduced repair in two cell lines, JIM1 and JIM3, and in two of four PCL cases and was associated with aberrant expression of at least one mismatch repair protein. Thus we show that MMR defects are found in plasma cell dyscrasias and the increased frequency during more active stages of the disease suggests a contributory role in disease progression.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
P. J. Hayden, P. Tewari, D. W. Morris, A. Staines, D. Crowley, A. Nieters, N. Becker, S. de Sanjose, L. Foretova, M. Maynadie, et al.
Variation in DNA repair genes XRCC3, XRCC4, XRCC5 and susceptibility to myeloma
Hum. Mol. Genet., December 15, 2007; 16(24): 3117 - 3127.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
E. C. Matheson, L. A. Hogarth, M. C. Case, J. A.E. Irving, and A. G. Hall
DHFR and MSH3 co-amplification in childhood acute lymphoblastic leukaemia, in vitro and in vivo
Carcinogenesis, June 1, 2007; 28(6): 1341 - 1346.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.