Literature DB >> 8512811

Rapid detection of allele loss in colorectal tumours using microsatellites and fluorescent DNA technology.

L Cawkwell1, S M Bell, F A Lewis, M F Dixon, G R Taylor, P Quirke.   

Abstract

In order to investigate allele loss in colorectal tumours we have developed a rapid technique which overcomes most of the problems associated with radioactive Restriction Fragment Length Polymorphism (RFLP) analysis of allele loss. We utilise microsatellite length polymorphisms which are highly informative and are closely linked to loci of interest. Sequences containing microsatellites can be amplified from normal and tumour DNA pairs by a polymerase chain reaction (PCR) in which one of the primers is fluorescently labelled. This enables us to detect the products on polyacrylamide gels run on an automated DNA sequencer using dedicated software, by which results are automatically quantitated in terms of peak size, height, and area. Using this technique we have analysed 26 normal tissue: cancer pairs for allele loss at two loci linked to the adenomatous polyposis coli (APC) gene on chromosome 5q. Repeated assays yielded identical results for each pair. Allele loss was found in 10 out of 25 informative samples (40%).

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Year:  1993        PMID: 8512811      PMCID: PMC1968523          DOI: 10.1038/bjc.1993.236

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  14 in total

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Authors:  J L Weber; P E May
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Authors:  P Laurent-Puig; S Olschwang; O Delattre; Y Remvikos; B Asselain; T Melot; P Validire; M Muleris; J Girodet; R J Salmon
Journal:  Gastroenterology       Date:  1992-04       Impact factor: 22.682

3.  Detection of loss of heterozygosity at the human TP53 locus using a dinucleotide repeat polymorphism.

Authors:  M H Jones; Y Nakamura
Journal:  Genes Chromosomes Cancer       Date:  1992-07       Impact factor: 5.006

4.  CA repeat polymorphism at the D5S299 locus linked to adenomatous polyposis coli (APC).

Authors:  C van Leeuwen; C Tops; C Breukel; H van der Klift; R Fodde; P M Khan
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

5.  Identification of FAP locus genes from chromosome 5q21.

Authors:  K W Kinzler; M C Nilbert; L K Su; B Vogelstein; T M Bryan; D B Levy; K J Smith; A C Preisinger; P Hedge; D McKechnie
Journal:  Science       Date:  1991-08-09       Impact factor: 47.728

6.  Chromosome 5 allele loss in human colorectal carcinomas.

Authors:  E Solomon; R Voss; V Hall; W F Bodmer; J R Jass; A J Jeffreys; F C Lucibello; I Patel; S H Rider
Journal:  Nature       Date:  1987 Aug 13-19       Impact factor: 49.962

7.  Cancer. Gene losses in human tumours.

Authors:  B Ponder
Journal:  Nature       Date:  1988-09-29       Impact factor: 49.962

8.  CA repeat polymorphism at the D5S82 locus, proximal to adenomatous polyposis coli (APC).

Authors:  C Breukel; C Tops; C van Leeuwen; H van der Klift; Y Nakamura; R Fodde; P M Khan
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

9.  High frequency of APC loss in sporadic colorectal carcinoma due to breaks clustered in 5q21-22.

Authors:  P G Ashton-Rickardt; M G Dunlop; Y Nakamura; R G Morris; C A Purdie; C M Steel; H J Evans; C C Bird; A H Wyllie
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10.  c-Ki-ras gene mutations in dysplasia and carcinomas complicating ulcerative colitis.

Authors:  S M Bell; S A Kelly; J A Hoyle; F A Lewis; G R Taylor; H Thompson; M F Dixon; P Quirke
Journal:  Br J Cancer       Date:  1991-07       Impact factor: 7.640

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  42 in total

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6.  Losses at 3p common deletion sites in subtypes of kidney tumours: histopathological correlations.

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7.  Expression of SMARCF1, a truncated form of SWI1, in neuroblastoma.

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8.  Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.

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9.  Frequency of replication errors in colorectal cancer and their association with family history.

Authors:  S R Brown; P J Finan; L Cawkwell; P Quirke; D T Bishop
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10.  Allelic imbalance and microsatellite instability of the DCC gene in colorectal cancer in patients under the age of 35 using fluorescent DNA technology.

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