Semiquantitative assessment of immunohistochemistry for mismatch repair proteins in Lynch syndrome

被引:30
作者
Barrow, Emma [1 ]
Jagger, Emma [2 ]
Brierley, Judith [2 ]
Wallace, Andrew [3 ]
Evans, Gareth [4 ,5 ,6 ]
Hill, James [1 ]
McMahon, Ray [2 ,7 ]
机构
[1] Manchester Royal Infirm, Dept Gen Surg, Manchester M13 9WL, Lancs, England
[2] Manchester Royal Infirm, Dept Pathol, Manchester M13 9WL, Lancs, England
[3] St Marys Hosp, NW Reg Mol Genet Serv, Natl Genet Reference Lab Manchester, Manchester M13 0JH, Lancs, England
[4] Univ Manchester, Med Genet Res Grp, Manchester, Lancs, England
[5] Univ Manchester, Reg Genet Serv, Manchester, Lancs, England
[6] St Marys Hosp, Cent Manchester & Manchester Childrens Univ Hosp, Manchester M13 0JH, Lancs, England
[7] Univ Manchester, Sch Med, Fac Med & Human Sci, Manchester, Lancs, England
关键词
biological markers; DNA mismatch repair; evaluation studies; hereditary non-polyposis colorectal cancer; immunohistochemistry; Lynch syndrome; MICROSATELLITE-INSTABILITY; COLORECTAL-CANCER; ESTROGEN-RECEPTOR; COLON-CANCER; HMLH1; PROMOTER; GENE-MUTATIONS; MLH1; PMS2; EXPRESSION; TUMORS;
D O I
10.1111/j.1365-2559.2010.03485.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To assess semiquantitative immunohistochemistry as used in the diagnosis of Lynch syndrome. Methods and Results: Tumour sections from 51 mutation carriers and 17 controls were stained with antibodies against MLII1, MSII2, MSII6 and PMS2. Intensity of immunoreactivity and percentage positivity were recorded on scales of 0-3 and 0-4, respectively. These scores were multiplied for a score of 0-12 per slide. Receiver-operator characteristic (ROC) curves of staining performance for the identification of mutation carriers were evaluated, and optimum cut-offs calculated. The area under the MLH1 ROC curve was 0.981 [95% confidence interval (CI) 0.952, 1.000]. The area under the MSH2 ROC curve was 0.899 (95% CI 0.796, 1.000). For MLH1 staining, a score <= 4 gives a sensitivity of 100.0% (95% CI 84.0, 100.0) and a specificity of 91.5% (95% CI 79.6, 97.6) for identifying MLH1 mutation carriers. For MSH2 staining, a score <= 4 gives a sensitivity of 87.5% (95% CI 61.7, 98.4) and specificity of 88.5% (95% CI 76.5, 95.6) for identifying MSH2 mutation carriers. Conclusions: This study supports a semiquantitative slide assessment method. Protein expression may occur in the context of known pathogenic mutations, a potential pitfall in the screening process.
引用
收藏
页码:331 / 344
页数:14
相关论文
共 40 条
[1]  
AALTONEN LA, 1994, CANCER RES, V54, P1645
[2]   DIAGNOSTIC-TESTS-3 - RECEIVER OPERATING CHARACTERISTIC PLOTS .7. [J].
ALTMAN, DG ;
BLAND, JM .
BRITISH MEDICAL JOURNAL, 1994, 309 (6948) :188-188
[3]   Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer [J].
Barnetson, Rebecca A. ;
Cartwright, Nicola ;
van Vliet, Annelot ;
Haq, Naila ;
Drew, Kate ;
Farrington, Susan ;
Williams, Nicola ;
Warner, Jon ;
Campbell, Harry ;
Porteous, Mary E. ;
Dunlop, Malcolm G. .
HUMAN MUTATION, 2008, 29 (03) :367-374
[4]   Identification and survival of carriers of mutations in DNA mismatch-repair genes in colon cancer [J].
Barnetson, Rebecca A. ;
Tenesa, Albert ;
Farrington, Susan M. ;
Nicholl, Iain D. ;
Cetnarskyj, Roseanne ;
Porteous, Mary E. ;
Campbell, Harry ;
Dunlop, Malcolm G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (26) :2751-2763
[5]   DNA markers predicting benefit from adjuvant fluorouracil in patients with colon cancer: a molecular study [J].
Barratt, PL ;
Seymour, MT ;
Stenning, SP ;
Georgiades, I ;
Walker, C ;
Birbeck, K ;
Quirke, P .
LANCET, 2002, 360 (9343) :1381-1391
[6]   Cost analysis of biomarker testing for mismatch repair deficiency in node-positive colorectal cancer [J].
Barrow, E. ;
McMahon, R. ;
Evans, D. G. ;
Levine, E. ;
Hill, J. .
BRITISH JOURNAL OF SURGERY, 2008, 95 (07) :868-875
[7]  
Boland CR, 1998, CANCER RES, V58, P5248
[8]   Antibody-based screening for hereditary nonpolyposis colorectal carcinoma compared with microsatellite analysis and sequencing [J].
Christensen, M ;
Katballe, N ;
Wikman, F ;
Primdahl, H ;
Sorensen, FB ;
Laurberg, S ;
Orntoft, TF .
CANCER, 2002, 95 (11) :2422-2430
[9]  
Cunningham JM, 1998, CANCER RES, V58, P3455
[10]   Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer [J].
de Jong, AE ;
van Puijenbroek, M ;
Hendriks, Y ;
Tops, C ;
Wijnen, J ;
Ausems, MGEM ;
Meijers-Heijboer, H ;
Wagner, A ;
van Os, TAM ;
Bröcker-Vriends, AHJT ;
Vasen, HFA ;
Morreau, H .
CLINICAL CANCER RESEARCH, 2004, 10 (03) :972-980