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Microsatellite instability markers in breast cancer: A review and study showing MSI was not detected at ‘BAT 25’ and ‘BAT 26’ microsatellite markers in early-onset breast cancer

Overview of attention for article published in Breast Cancer Research and Treatment, March 2000
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Title
Microsatellite instability markers in breast cancer: A review and study showing MSI was not detected at ‘BAT 25’ and ‘BAT 26’ microsatellite markers in early-onset breast cancer
Published in
Breast Cancer Research and Treatment, March 2000
DOI 10.1023/a:1006315315060
Pubmed ID
Authors

Shoo Peng Siah, Shoo Peng Siah, Diana M Quinn, Graeme D Bennett, Graeme Casey, Robert LP Flower, Graeme Suthers, Zbigniew Rudzki

Abstract

Microsatellite markers may provide evidence of faulty DNA mismatch repair (MMR) via the detection of microsatellite instability (MSI). The choice of microsatellite markers may impact on the MSI detection rate. In hereditary non-polyposis colon cancer (HNPCC), several informative microsatellite markers have been recommended. Two of these, BAT 25 and BAT 26, are quasi-homozygous, enabling analysis of tumour DNA in the absence of paired normal DNA. Sixty-six breast cancer patients under 45 years of age at diagnosis were examined for MSI at BAT 25 and BAT 26. Tumour DNA was extracted from paraffin-embedded tissue. No MSI was detected at the BAT 25 or BAT 26 loci. An additional five microsatellite markers, known to be informative for HNPCC, were examined for MSI in these patients. Apparently-normal profiles were achieved. A tabulated survey of 306 microsatellite markers used to detect MSI in breast cancer revealed that only 35.5% of markers detected MSI at an average rate of 2.9%. The MSI detection rate at the specific HNPCC markers varied from 0% to 10% in breast cancer, with D175250 and TP53 being the HNPCC markers most suitable for analysis of breast cancer. The size of the microsatellite marker's repeat unit did not impact on MSI detection rates. Compiled data from large studies (n > 100) revealed D115988 as the marker with the highest MSI detection rate. Genomic instability pathways of carcinogenesis, characterised by MMR defects and MSI, appear to play a role in the genesis of some breast cancer types.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 32 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
China 1 3%
Brazil 1 3%
Unknown 30 94%

Demographic breakdown

Readers by professional status Count As %
Other 5 16%
Student > Ph. D. Student 5 16%
Researcher 4 13%
Professor > Associate Professor 4 13%
Student > Master 3 9%
Other 5 16%
Unknown 6 19%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 8 25%
Medicine and Dentistry 8 25%
Agricultural and Biological Sciences 5 16%
Sports and Recreations 1 3%
Computer Science 1 3%
Other 2 6%
Unknown 7 22%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 22 July 2014.
All research outputs
#7,512,050
of 22,947,506 outputs
Outputs from Breast Cancer Research and Treatment
#1,668
of 4,670 outputs
Outputs of similar age
#12,846
of 40,415 outputs
Outputs of similar age from Breast Cancer Research and Treatment
#3
of 13 outputs
Altmetric has tracked 22,947,506 research outputs across all sources so far. This one is in the 44th percentile – i.e., 44% of other outputs scored the same or lower than it.
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