Ulcerative colitis and colorectal carcinoma -: DNA-profile, laminin-5 γ2 chain and cyclin A expression as early markers for risk assessment

被引:30
作者
Habermann, J
Lenander, C
Roblick, UJ
Krüger, S
Ludwig, D
Alaiya, A
Freitag, S
Dümbgen, L
Bruch, HP
Stange, E
Salo, S
Tryggvason, K
Auer, G [1 ]
Schimmelpenning, H
机构
[1] Karolinska Hosp, Dept Oncol & Pathol, Div Cellular & Mol Tumor Pathol, SE-17176 Stockholm, Sweden
[2] Ersta Hosp, Dept Surg, Stockholm, Sweden
[3] Med Univ Lubeck, Dept Pathol, D-23538 Lubeck, Germany
[4] Med Univ Lubeck, Dept Gastroenterol, D-23538 Lubeck, Germany
[5] Med Univ Lubeck, Dept Surg, D-23538 Lubeck, Germany
[6] Med Univ Lubeck, Inst Math, D-23538 Lubeck, Germany
[7] Karolinska Inst, Dept Med Biochem & Biophys, Div Matrix Biol, Stockholm, Sweden
关键词
carcinoma; cyclin A; DNA ploidy; laminin-5; gamma; 2; chain; risk factors; ulcerative colitis;
D O I
10.1080/003655201300192021
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Ulcerative colitis patients are at increased risk for developing colorectal carcinomas. Despite expensive surveillance programmes, clinical practice reflects an uncertainty in individual risk assessment. The aim of the study was to evaluate independent cellular features with possible predictive value. Methods: Two patient groups were selected: group A comprised 8 patients with ulcerative colitis-associated colorectal carcinomas, group B comprised 16 ulcerative colitis patients with risk factors (duration of disease, extent of inflammation, epithelial dysplasias). A total of 683 paraffin-embedded mucosal biopsies were retrospectively evaluated for inflammatory activity, grade of dysplasia. ploidy status, laminin-5 gamma2 chain and cyclin A expression. Results: Mild or moderate inflammatory activity was present in 78% of all biopsies. low- or high-grade dysplasia in 5.5%. There was no difference in inflammatory activity and dysplasia between patient groups. In group A. 75% of the biopsies exhibited aneuploid DNA distribution patterns. Group B showed mainly proliferative-diploid cell populations (85% / P = 0.006). Laminin-5 gamma2 chain was expressed in 13% of all biopsies, with a higher frequency in group A (P = 0.002). Cyclin A expression was found in 98% of all biopsies, with a higher number of immunopositive cells in group A biopsies (P = 0.014). Conclusions: Combined nuclear DNA assessment, laminin-5 gamma2 chain and cyclin A expression may help to identify ulcerative colitis patients with an increased risk for cancer development.
引用
收藏
页码:751 / 758
页数:8
相关论文
共 32 条
  • [11] Molecular cloning and tissue-specific expression of a novel murine laminin γ3 chain
    Iivanainen, A
    Morita, T
    Tryggvason, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (20) : 14107 - 14111
  • [12] EXPRESSION OF INTEGRINS AND BASEMENT-MEMBRANE COMPONENTS BY WOUND KERATINOCYTES
    LARJAVA, H
    SALO, T
    HAAPASALMI, K
    KRAMER, RH
    HEINO, J
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (03) : 1425 - 1435
  • [13] DNA ANEUPLOIDY IN ULCERATIVE-COLITIS - REPRODUCIBILITY, TOPOGRAPHIC DISTRIBUTION, AND RELATION TO DYSPLASIA
    LOFBERG, R
    BROSTROM, O
    KARLEN, P
    OST, A
    TRIBUKAIT, B
    [J]. GASTROENTEROLOGY, 1992, 102 (04) : 1149 - 1154
  • [14] FAILURE OF COLONOSCOPIC SURVEILLANCE IN ULCERATIVE-COLITIS
    LYNCH, DAF
    LOBO, AJ
    SOBALA, GM
    DIXON, MF
    AXON, ATR
    [J]. GUT, 1993, 34 (08) : 1075 - 1080
  • [15] ONO J, 1984, CANCER, V54, P1030, DOI 10.1002/1097-0142(19840915)54:6<1030::AID-CNCR2820540617>3.0.CO
  • [16] 2-9
  • [17] PYKE C, 1995, CANCER RES, V55, P4132
  • [18] PYKE C, 1994, AM J PATHOL, V145, P782
  • [19] RIDELL RH, 1983, HUM PATHOL, V14, P931
  • [20] DNA ANEUPLOIDY IN COLONIC BIOPSIES PREDICTS FUTURE-DEVELOPMENT OF DYSPLASIA IN ULCERATIVE-COLITIS
    RUBIN, CE
    HAGGITT, RC
    BURMER, GC
    BRENTNALL, TA
    STEVENS, AC
    LEVINE, DS
    DEAN, PJ
    KIMMEY, M
    PERERA, DR
    RABINOVITCH, PS
    [J]. GASTROENTEROLOGY, 1992, 103 (05) : 1611 - 1620