Clinicopathological significance of microsatellite instability and mutated RIZ in colorectal cancer

被引:28
作者
Emterling, A
Wallin, Å
Arbman, G
Sun, XF [1 ]
机构
[1] Linkoping Univ, Dept Oncol, S-58185 Linkoping, Sweden
[2] Vrinnevi Hosp, Dept Surg, Norrkoping, Sweden
关键词
colorectal cancer; microsatellite instability; RIZ;
D O I
10.1093/annonc/mdh045
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Several studies have shown that microsatellite instability (MSI) is related to favourable survival in colorectal cancer patients but there are controversial results. Tumour suppressor gene RIZ is a susceptible mutational target of MSI. However, its clinicopathological significance has not been investigated. We investigated the prognostic significance of MSI in Swedish colorectal cancer patients and the clinicopathological significance of RIZ mutations. Patients and methods: We analysed 438 colorectal adenocarcinomas for MSI by microsatellite analysis. Among them, 29 MSI and 28 microsatellite stable (MSS) tumours were examined for RIZ mutations by DNA sequencing. Results: MSI (13% of 438 cases) was not associated with survival (rate ratio = 0.97, 95% confidence interval = 0.57-1.64, P = 0.90), although it was related to proximal tumour (P <0.001), poor differentiation and mucinous carcinomas (P <0.001), multiple tumours (P = 0.01) and negative/weak expression of hMLH1 (P = 0.03). RIZ mutations were detected in 31% of 29 MSI tumours but in none of the 28 MSS tumours. The mutations were related to female (P = 0.01), proximal turnout (P = 0.01), stage B (P = 0.01) and poor differentiation (P = 0.047). Conclusions: MSI was not a prognostic factor in the Swedish patients included in this study. Clinicopathological variables associated with RIZ mutations might be a consequence of the MSI characteristics.
引用
收藏
页码:242 / 246
页数:5
相关论文
共 29 条
[1]   Physical mapping of the retinoblastoma interacting zinc finger gene RIZ to D1S228 on chromosome 1p36 [J].
Buyse, IM ;
Takahashi, E ;
Huang, S .
GENOMICS, 1996, 34 (01) :119-121
[2]   Candidate tumor suppressor RIZ is frequently involved in colorectal carcinogenesis [J].
Chadwick, RB ;
Jiang, CL ;
Bennington, GA ;
Yuan, B ;
Johnson, CK ;
Stevens, MW ;
Niemann, TH ;
Peltomaki, P ;
Huang, S ;
de la Chapelle, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2662-2667
[3]  
Cravo M, 1999, J PATHOL, V188, P252, DOI 10.1002/(SICI)1096-9896(199907)188:3<252::AID-PATH354>3.0.CO
[4]  
2-3
[5]   Replication error phenotype, clinicopathological variables, and patient outcome in Dukes' B stage II (T3,N0,M0) colorectal cancer [J].
Curran, B ;
Lenehan, K ;
Mulcahy, H ;
Tighe, O ;
Bennett, MA ;
Kay, EW ;
O'Donoghue, DP ;
Leader, M ;
Croke, DT .
GUT, 2000, 46 (02) :200-204
[6]   Association of tumour site and sex with survival benefit from adjuvant chemotherapy in colorectal cancer [J].
Elsaleh, H ;
Joseph, D ;
Grieu, F ;
Zeps, N ;
Spry, N ;
Iacopetta, B .
LANCET, 2000, 355 (9217) :1745-1750
[7]  
Feeley KM, 1999, J PATHOL, V188, P14, DOI 10.1002/(SICI)1096-9896(199905)188:1<14::AID-PATH323>3.0.CO
[8]  
2-Q
[9]  
Gafà R, 2000, CANCER, V89, P2025, DOI 10.1002/1097-0142(20001115)89:10<2025::AID-CNCR1>3.0.CO
[10]  
2-S