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Frequent loss of SMAD4/DPC4 protein in colorectal cancers

Salovaara, R. (author)
Roth, S. (author)
Loukola, A. (author)
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Launonen, V. (author)
Sistonen, P. (author)
Avizienyte, E. (author)
Kristo, P. (author)
Järvinen, H. (author)
Souchelnytskyi, Serhiy (author)
Karolinska Institutet,Uppsala universitet,Ludwiginstitutet för cancerforskning
Sarlomo-Rikala, M. (author)
Aaltonen, L.A. (author)
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 (creator_code:org_t)
BMJ, 2002
2002
English.
In: Gut. - : BMJ. - 0017-5749 .- 1468-3288. ; 51:1, s. 56-59
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND AND AIMS: Loss of DNA sequences from chromosome 18q21 is a major genetic change in colorectal tumorigenesis. Multiple genes have been identified in this area. One of these, DPC4 (deleted in pancreatic cancer 4, also known as SMAD4), is mutated in a minor subset of colorectal carcinomas as well as in germlines of humans predisposed to colon tumours. PATIENTS AND METHODS: The involvement of SMAD4 in sporadic colorectal neoplasia was evaluated by immunohistochemistry in 53 unselected cases and 27 cases displaying microsatellite instability. RESULTS: SMAD4 expression was absent in 20 of 53 (38%) unselected colorectal carcinomas, and reduced in another 15 (28%) cases. However, 26 of 27 cancers displaying microsatellite instability and TGF-betaIIR mutations were positive for SMAD4 immunostaining. CONCLUSIONS: Loss of SMAD4 expression may play a more prominent role in colon cancer than anticipated based on genetic evidence, but not in mutator phenotype tumours.

Keyword

Chromosomes; Human; Pair 18/*genetics
Colorectal Neoplasms/chemistry/*genetics
DNA Mutational Analysis
DNA-Binding Proteins/analysis/*genetics
Gene Deletion
Genetic Markers
Humans
Immunohistochemistry/methods
Loss of Heterozygosity
Microsatellite Repeats
Receptors; Transforming Growth Factor beta/genetics
Smad4 Protein
Trans-Activators/analysis/*genetics

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art (subject category)

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