Down-regulation of p21 (CDKNIA/CIP1) is inversely associated with microsatellite instability and CpG island methylator phenotype (CIMP) in colorectal cancer

被引:61
|
作者
Ogino, S.
Kawasaki, T.
Kirkner, G. J.
Ogawa, A.
Dorfman, I.
Loda, M.
Fuchs, C. S.
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Pathol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
来源
JOURNAL OF PATHOLOGY | 2006年 / 210卷 / 02期
关键词
DNA methylation; colon cancer; MethyLight; p21; p53; MSI; CIMP; BRAF; WAF1; KRAS;
D O I
10.1002/path.2030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
p2l (CDKN1A/CIP1/WAF1), one of the cyclin-dependent kinase inhibitors, plays a key role in regulating the cell cycle and is transcriptionally regulated by p53. Down-regulation of p21 is caused by TP53 mutations in colorectal cancer. CpG island methylator phenotype (CIMP) appears to be a distinct subtype of colorectal cancer with concordant methylation of multiple gene promoters and is associated with a high degree of microsatellite instability (NISI-H) and BKAF mutations. However, no study to date has evaluated the relationship between p21 expression and CIMP in colorectal cancer. The purpose of this study was to examine the inter-relationships between p21, p53, CIMP, MSI and KRAS/BRAF status in colorectal cancer. We utilized 737 relatively unbiased samples of colorectal cancers from two large prospective cohort studies. Using quantitative real-time PCR (MethyLight), we measured DNA methylation in five CIMP-specific gene promoters [CACNA1G, CDKN2A (p16/INK4A), CPABP1, MLH1 and NEUROG1]. CIMP-high (>= 415 methylated promoters) was diagnosed in 118 (16%) of the 737 tumours. We also assessed expression of p21 and p53 by immunohistochemistry. Among the 737 tumours, 371 (50%) showed p21 loss. Both p21 loss and p53 positivity were inversely associated with CIMP-high, MSI-H and BPAF mutations. The associations of p21 with these molecular features were still present after tumours were stratified by p53 status. In contrast, the associations of p53 positivity with the molecular features were no longer present after tumours were stratified by p21 status. When CIMP-high and non-CIMP-high tumours were stratified by MSI or KPAS/BRAF status, CIMP-high and MSI-H (but not BPAF mutations) were still inversely associated with p21 loss. In conclusion, down-regulation of p21 is inversely correlated with CIMP-high and MSI-H in colorectal cancer, independent of TP53 and BRAF status. Copyright (c) 2006 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
引用
收藏
页码:147 / 154
页数:8
相关论文
共 50 条
  • [1] Down-regulation of p21 (CDKN1A/CIP1) in colorectal cancer is inversely associated with MS1 and CpG island methylator phenotype (CIMP) determined by quantitative DNA methylation analysis
    Ogino, S.
    Kawasaki, T.
    Loda, M.
    Fuchs, C.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2006, 8 (05): : 657 - 657
  • [2] Tetranucleotide and Low Microsatellite Instability Are Inversely Associated with the CpG Island Methylator Phenotype in Colorectal Cancer
    Meessen, Sabine
    Currey, Nicola
    Jahan, Zeenat
    Parker, Hannah W.
    Jenkins, Mark A.
    Buchanan, Daniel D.
    Hopper, John L.
    Segelov, Eva
    Dahlstrom, Jane E.
    Kohonen-Corish, Maija R. J.
    CANCERS, 2021, 13 (14)
  • [3] LINE-1 hypomethylation is inversely associated with microsatellite instability and CpG island methylator phenotype in colorectal cancer
    Ogino, Shuji
    Kawasaki, Takako
    Nosho, Katsuhiko
    Ohnishi, Mutsuko
    Suemoto, Yuko
    Kirkner, Gregory J.
    Fuchs, Charles S.
    INTERNATIONAL JOURNAL OF CANCER, 2008, 122 (12) : 2767 - 2773
  • [4] Fatty acid synthase overexpression in colorectal cancer is associated with microsatellite instability, independent of CpG island methylator phenotype (CIMP)
    Kawasaki, T.
    Fuchs, C. S.
    Loda, M.
    Ogino, S.
    LABORATORY INVESTIGATION, 2007, 87 : 119A - 119A
  • [5] Fatty acid synthase overexpression in colorectal cancer is associated with microsatellite instability, independent of CpG island methylator phenotype (CIMP)
    Kawasaki, T.
    Fuchs, C. S.
    Loda, M.
    Ogino, S.
    MODERN PATHOLOGY, 2007, 20 : 119A - 119A
  • [6] The CpG island methylator phenotype and chromosomal instability are inversely correlated in sporadic colorectal cancer
    Goel, Ajay
    Nagasaka, Takeshi
    Arnold, Christian N.
    Inoue, Toru
    Hamilton, Cody
    Niedzwiecki, Donna
    Compton, Carolyn
    Mayer, Robert J.
    Goldberg, Richard
    Bertagnolli, Monica M.
    Boland, C. Richard
    GASTROENTEROLOGY, 2007, 132 (01) : 127 - 138
  • [7] The impact of CpG island methylator phenotype and microsatellite instability on tumour budding in colorectal cancer
    Zlobec, Inti
    Bihl, Michel P.
    Foerster, Anja
    Rufle, Alex
    Lugli, Alessandro
    HISTOPATHOLOGY, 2012, 61 (05) : 777 - 787
  • [8] Impact of CpG island methylator phenotype and microsatellite instability on tumor budding in colorectal cancer
    Zlobec, I.
    Bihl, M.
    Koelzer, V.
    Foerster, A.
    Rufle, A.
    Lugli, A.
    VIRCHOWS ARCHIV, 2011, 459 : S19 - S20
  • [9] Do histopathologic features of colorectal carcinoma predict microsatellite instability (MSI) or CpG island methylator phenotype (CIMP) or both?
    Ogino, S.
    Loda, M.
    Fuchs, C. S.
    MODERN PATHOLOGY, 2007, 20 : 126A - 126A
  • [10] Do histopathologic features of colorectal carcinoma predict microsatellite instability (MSI) or CpG island methylator phenotype (CIMP) or both?
    Ogino, S.
    Loda, M.
    Fuchs, C. S.
    LABORATORY INVESTIGATION, 2007, 87 : 126A - 126A