An evaluation and replication of miRNAs with disease stage and colorectal cancer-specific mortality.
An evaluation and replication of miRNAs with disease stage and colorectal cancer-specific mortality.
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具有疾病期和结直肠癌特异性死亡率的miRNA的评估和复制。
DOI:
10.1002/ijc.29384
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发表时间:
2015-07-15
影响因子:
6.4
通讯作者:
Wolff, Roger K.
中科院分区:
文献类型:
--
作者:
Slattery, Martha L.;Herrick, Jennifer S.;Mullany, Lila E.;Valeri, Nicola;Stevens, John;Caan, Bette J.;Samowitz, Wade;Wolff, Roger K.
MiRNAs have been implicated in CRC development and associated with prognostic indicators such as disease stage and survival. Prognostic associations are often based on few individuals and imprecise. In this study, we utilize population-based data from 1141 colorectal cancer (CRC) cases to replicate previously reported associations between 121 miRNAs and disease stage and survival. The Agilent Human miRNA Microarray V19.0 was used to generate miRNA data following a stringent quality control protocol. Assessment of survival was done using Cox Proportional Hazard models adjusting for age, disease stage, and tumor molecular phenotype. Five miRNAs were associated with more advanced disease stage; hsa-miR-145-5p and hsa-miR-31-5p showed increased expression with more advanced tumor stage, while hsa-miR-200b-3p, hsa-miR-215, and hsa-miR-451a had decreased expression with more advanced tumors. Thirteen miRNAs were associated with colorectal cancer mortality among individuals diagnosed with colon cancer while fourteen were associated with colorectal cancer mortality after a diagnosis with rectal cancer. Strongest associations were observed for those miRNAs that were expressed in a small subset of tumors. Most notable associations were for hsa-miR-145-3p (HR 2.94 95% CI 1.54, 5.61), and hsa-miR-9-3p (HR 10.28 95% CI1.31 80.84) with colon cancer and hsa-miR-335-5p (HR 0.17 95% CI 0.05, 0.54) for rectal cancer. Hsa-miR-374a-5p, hsa-miR-570-3p and hsa-miR-18a-5p significantly reduced the hazard of dying for all cases, regardless of tumor site. Our findings illustrate the need for a large sample to evaluate the association of miRNAs with survival and disease stage in order to determine associations by tumor site.
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影响因子:
4.3
作者:
Oliveras-Ferraros, Cristina;Cufi, Slvia;Menendez, Javier A.
通讯作者:
Menendez, Javier A.
影响因子:
3.9
作者:
Knowlton, David L.;Tang, Kim;Subramanian, Romesh R.
通讯作者:
Subramanian, Romesh R.
影响因子:
14.9
作者:
Hsu SD;Tseng YT;Shrestha S;Lin YL;Khaleel A;Chou CH;Chu CF;Huang HY;Lin CM;Ho SY;Jian TY;Lin FM;Chang TH;Weng SL;Liao KW;Liao IE;Liu CC;Huang HD
通讯作者:
Huang HD
影响因子:
14.9
作者:
Griffiths-Jones S;Grocock RJ;van Dongen S;Bateman A;Enright AJ
通讯作者:
Enright AJ
影响因子:
29.4
作者:
Liang, Li;Li, Xianzheng;Ding, Yanqing
通讯作者:
Ding, Yanqing