miR-429 Identified by Dynamic Transcriptome Analysis Is a New Candidate Biomarker for Colorectal Cancer Prognosis

被引:42
作者
Sun, Yingnan [1 ,2 ]
Shen, Shourong [1 ,2 ]
Tang, Hailin [3 ,4 ,5 ,8 ]
Xiang, Juanjuan [2 ,3 ,4 ,5 ]
Peng, Ya [6 ]
Tang, Anliu [1 ,2 ]
Li, Nan [1 ,2 ]
Zhou, Weiwei [1 ,2 ]
Wang, Zeyou [3 ,4 ,5 ]
Zhang, Decai [1 ,2 ]
Xiang, Bo [2 ,3 ,4 ,5 ]
Ge, Jie [7 ]
Li, Guiyuan [2 ,3 ,4 ,5 ]
Wu, Minghua [1 ,2 ,3 ,4 ,5 ]
Li, Xiayu [1 ,2 ]
机构
[1] Cent S Univ, Xiangya Hosp 3, Dept Gastroenterol, Changsha 410013, Hunan, Peoples R China
[2] Hunan Key Lab Nonresolving Inflammat & Canc, Changsha, Hunan, Peoples R China
[3] Cent S Univ, Minist Educ, Key Lab Carcinogenesis & Canc Invas, Changsha 410013, Hunan, Peoples R China
[4] Cent S Univ, Minist Hlth, Key Lab Carcinogenesis, Changsha 410013, Hunan, Peoples R China
[5] Cent S Univ, Canc Res Inst, Changsha 410013, Hunan, Peoples R China
[6] Hunan Normal Univ, Hunan Prov Peoples Hosp, Dept Digest Dis, Changsha, Hunan, Peoples R China
[7] Cent S Univ, Xiangya Hosp, Dept Gastrointestinal Surg, Changsha 410013, Hunan, Peoples R China
[8] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Guangzhou 510275, Guangdong, Peoples R China
基金
美国国家科学基金会;
关键词
GENE-EXPRESSION; NONCODING RNAS; PROFILES; MICRORNAS; BIOLOGY; TOOL;
D O I
10.1089/omi.2012.0132
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Colorectal cancer (CRC) is a common malignant gastrointestinal cancer. Efforts for preventive and personalized medicine have intensified in the last decade with attention to novel forms of biomarkers. In the present study, microRNA and genetic analyses were performed in tandem for differential transcriptome profiling between primary tumors with or without nodes or distant metastases. Serial Test Cluster (STC) analysis demonstrated that 20 genes and two microRNAs showed distinctive expression patterns associated with the tumor, node, and metastasis (TNM) stage. The selected target genes were characterized by GO and Pathway analysis. A microRNA-target gene network analysis showed that miR-429 resided in the center of the network, indicating that miR-429 might serve important roles in the development of CRC. Real-time PCR and tissue microarrays showed that miR-429 had a dynamic expression pattern during the CRC progression stage, and was significantly downregulated in stage II and stage III clinical progression. The low expression of miR-429 was correlated with poor prognosis for CRC. Taken together, miR-429 warrant further clinical translation research as a candidate biomarker for CRC prognosis. Additional downstream targets and attendant gene function also need to be discerned to design a sound critical path to personalized medicine for persons susceptible to, or diagnosed with CRC.
引用
收藏
页码:54 / 64
页数:11
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