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Detection of Ki-ras gene point mutations in bile specimens for the differential diagnosis of malignant and benign biliary strictures
  1. J-C Saurina,
  2. M-O Joly-Pharabozb,
  3. P Pernasb,c,
  4. L Henrya,
  5. T Ponchona,
  6. J-J Madjarb,c
  1. aFédération des Spécialités Digestives, Hôpital Edouard Herriot, Lyon, France, bFédération de Biochimie, Hôpital Edouard Herriot, Lyon, France, cINSERM U 369, Faculté de Médecine Lyon-RTH Laennec, Lyon, France
  1. Dr J C Saurin, Fédération des Spécialités Digestives, Hôpital Edouard-Herriot, Pavillon O, 69437 Lyon Cedex 03, France. Email: saurin{at}lyon151.inserm.fr

Abstract

BACKGROUND AND AIM The present study was undertaken to determine if detection of Ki-ras gene point mutations in bile specimens could differentiate between benign and malignant biliary strictures.

PATIENTS Bile specimens were obtained from 117 patients exhibiting a stricture of the main bile duct, the nature of which was assessed by cholangiography, histology, and follow up.

METHODS DNA from frozen bile specimens was extracted, amplified, and tested for codon 12 point mutations of Ki-ras gene using sequence specific oligonucleotide hybridisation and mutant allele specific amplification.

RESULTS DNA amplification was successful in 110/117 bile specimens (94%). Detection of Ki-ras gene mutations in bile specimens was positive in 24.4% (22/90) of patients with malignant strictures, in 31.4% (22/70) when only primary malignant tumours were considered, and in 4% (1/25) of patients with benign strictures. Of the 49 patients with histological specimens obtained before surgery, the sensitivity of histology, Ki-rasmutation analysis, and combined methods was 59.2%, 28.6%, and 73.5% respectively.

CONCLUSIONS Our study showed that Ki-ras mutations may be detected in about one third of bile specimens from patients with primary tumours invading the main bile duct. Detection of such mutations appears to be specific and may help to differentiate between benign and malignant biliary strictures.

  • biliary strictures
  • bile specimens
  • Ki-ras gene mutations
  • Abbreviations used in this paper

    MASA
    mutant allele specific amplification
    PCR
    polymerase chain reaction
    SDS
    sodium dodecyl sulphate
    SSOH
    sequence specific oligonucleotide hybridisation
    SSC
    standard saline citrate
    UTP
    uridine 5′-triphosphate
    TTP
    thymidine 5′-triphosphate
    CT
    computed tomography
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  • Abbreviations used in this paper

    MASA
    mutant allele specific amplification
    PCR
    polymerase chain reaction
    SDS
    sodium dodecyl sulphate
    SSOH
    sequence specific oligonucleotide hybridisation
    SSC
    standard saline citrate
    UTP
    uridine 5′-triphosphate
    TTP
    thymidine 5′-triphosphate
    CT
    computed tomography
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