A molecular signature for the prediction of recurrence in colorectal cancer

被引:20
|
作者
Wang, Lisha [1 ,2 ,3 ]
Shen, Xiaohan [1 ,2 ,3 ]
Wang, Zhimin [5 ,6 ]
Xiao, Xiuying [7 ]
Wei, Ping [1 ,2 ,3 ]
Wang, Qifeng [1 ,2 ,3 ]
Ren, Fei [1 ,2 ,3 ]
Wang, Yiqin [1 ,2 ,3 ]
Liu, Zebing [1 ,2 ,3 ]
Sheng, Weiqi [1 ,2 ,3 ]
Huang, Wei
Zhou, Xiaoyan [1 ,2 ,3 ]
Du, Xiang [1 ,2 ,3 ,4 ]
机构
[1] Fudan Univ, Shanghai Canc Ctr, Dept Pathol, Shanghai 200032, Peoples R China
[2] Fudan Univ, Shanghai Canc Ctr, Dept Oncol, Shanghai 200032, Peoples R China
[3] Fudan Univ, Inst Pathol, Shanghai 200032, Peoples R China
[4] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[5] Chinese Natl Human Genome Ctr, Shanghai MOST Key Lab Hlth & Dis Genom, Dept Genet, Shanghai 201203, Peoples R China
[6] Shanghai Ind Technol Inst, Shanghai 201203, Peoples R China
[7] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Oncol, Shanghai 200127, Peoples R China
来源
MOLECULAR CANCER | 2015年 / 14卷
基金
中国国家自然科学基金;
关键词
Molecular signature; Gene expression; Colorectal cancer; Recurrence; CELL LUNG-CANCER; III COLON-CANCER; STAGE-II; GENE-EXPRESSION; MICROSATELLITE INSTABILITY; ADJUVANT THERAPY; PROGNOSIS; FLUOROURACIL; INHIBITORS; TISSUE;
D O I
10.1186/s12943-015-0296-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Several clinical and pathological factors have an impact on the prognosis of colorectal cancer (CRC), but they are not yet adequate for risk assessment. We aimed to identify a molecular signature that can reliably identify CRC patients at high risk for recurrence. Results: Two hundred eighty-one CRC samples (stage II/III) were included in this study. A two-step gene expression profiling study was conducted. First, gene expression measurements from 81 fresh frozen CRC samples were obtained using Affymetrix Human Genome U133 Plus 2.0 Arrays. Second, a focused gene expression assay, including prognostic genes and genes of interest from literature reviews, was performed using 200 fresh frozen samples and a Taqman low-density array (TLDA) analysis. An optimal 31-gene expression classifier for the prediction of recurrence among patients with stage II/III CRC was developed using logistic regression analysis. This gene expression signature classified 58.5% of patients as low-risk and 41.5% as high-risk (P < 0.001). The signature was the strongest independent prognostic factor in the multivariate analysis. The five-year relapse-free survival (RFS) rates for the low-risk patients and the high-risk patients were 88.5% and 41.3% (P < 0.001), respectively. Conclusion: We identified a 31-gene expression signature that is closely associated with the clinical outcome of stage II/III CRC patients.
引用
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页数:10
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