Insulin-like growth factor 2 messenger RNA binding protein 3 (IGF2BP3) is a marker of unfavourable prognosis in colorectal cancer

被引:86
|
作者
Lochhead, Paul [1 ,2 ]
Imamura, Yu [1 ,2 ]
Morikawa, Teppei [1 ,2 ]
Kuchiba, Aya [1 ,2 ,3 ]
Yamauchi, Mai [1 ,2 ]
Liao, Xiaoyun [1 ,2 ]
Qian, Zhi Rong [1 ,2 ]
Nishihara, Reiko [1 ,2 ,3 ]
Wu, Kana [3 ]
Meyerhardt, Jeffrey A. [1 ,2 ]
Fuchs, Charles S. [1 ,2 ,4 ]
Ogino, Shuji [1 ,2 ,5 ,6 ]
机构
[1] Dana Farber Canc Inst, Ctr Mol Oncol Pathol, Dept Med Oncol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Dept Med, Channing Lab, Boston, MA 02115 USA
[5] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
Adenocarcinoma; Rectal cancer; Cancer testis antigen; MAGE; Carcinogenesis; Diagnostic marker; Pathology; Therapeutic target; Personalised medicine; ISLAND METHYLATOR PHENOTYPE; MOLECULAR PATHOLOGICAL EPIDEMIOLOGY; COLON-CANCER; MICROSATELLITE INSTABILITY; IMP3; EXPRESSION; BRAF MUTATION; CARCINOMA; SURVIVAL; ADENOCARCINOMA; PROGRESSION;
D O I
10.1016/j.ejca.2012.06.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Evidence suggests that insulin-like growth factor 2 messenger RNA binding protein 3 (IGF2BP3, also known as IMP3) represents a promising cancer biomarker. However, the clinical, pathological, molecular and prognostic features of IGF2BP3-positive colorectal cancers remain uncertain. Materials and methods: We evaluated IGF2BP3 expression by immunohistochemistry in 671 rectal and colon cancer cases that form part of a molecular pathological epidemiology database. Cox proportional hazards regression models were used to compute mortality hazard ratio (HR), adjusting for clinical, pathological and molecular features, including microsatellite instability, the CpG island methylator phenotype, LINE-1 methylation and KRAS, BRAF and PIK3CA mutations. Results: Among 671 colorectal cancers, 234 (35%) tumours were positive for IGF2BP3. In contrast, normal colorectal epithelium was negative for IGF2BP3 in all 403 specimens of normal mucosa adjacent to carcinoma. IGF2BP3 positivity was associated with poor differentiation (p = 0.0003), stage III-IV disease (p = 0.0081), BRAF mutation (p = 0.031), and LINE-1 hypomethylation (p = 0.020). IGF2BP3 positivity was significantly associated with shorter colorectal cancer-specific [log-rank p < 0.0001; multivariate HR, 1.37; 95% confidence interval (CI), 1.02-1.84] and overall survival (log-rank p = 0.0004; multivariate HR, 1.32; 95% CI, 1.05-1.66). Conclusions: IGF2BP3 expression in colorectal cancer is associated with adverse clinical outcome. Our findings support a role for IGF2BP3 as a diagnostic and/or prognostic biomarker in colorectal cancer. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3405 / 3413
页数:9
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