MicroRNA Profiling and Head and Neck Cancer

被引:124
作者
Liu, Xiqiang [1 ,2 ,3 ]
Chen, Zugen [4 ,5 ]
Yu, Jinsheng [1 ]
Xia, James [6 ]
Zhou, Xiaofeng [1 ,2 ,3 ]
机构
[1] Univ Illinois, Grad Coll, Coll Dent, UIC Canc Ctr,Ctr Mol Biol Oral Dis, Chicago, IL 60612 USA
[2] Sun Yat Sen Univ, Res Inst Stomatol, Guangzhou 510055, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Guanghua Sch, Guangzhou 510055, Guangdong, Peoples R China
[4] Univ Calif Los Angeles, UCLA Microarray Core Facil, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
[6] GenoSensor Corp, Tempe, AZ 85282 USA
来源
COMPARATIVE AND FUNCTIONAL GENOMICS | 2009年
关键词
SQUAMOUS-CELL CARCINOMA; HUMAN BREAST-CANCER; GENE-EXPRESSION; HEPATOCELLULAR-CARCINOMA; HUMAN-PAPILLOMAVIRUS; DOWN-REGULATION; MICROARRAY PLATFORM; ANIMAL DEVELOPMENT; MIRNA EXPRESSION; CAPTURE PROBES;
D O I
10.1155/2009/837514
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
Head and neck/oral cancer (HNOC) is a devastating disease. Despite advances in diagnosis and treatment, mortality rates have not improved significantly over the past three decades. Improvement in patient survival requires a better understanding of the disease progression so that HNOC can be detected early in the disease process and targeted therapeutic interventions can be deployed. Accumulating evidence suggests that microRNAs play important roles in many human cancers. They are pivotal regulators of diverse cellular processes including proliferation, differentiation, apoptosis, survival, motility, and morphogenesis. MicroRNA expression patterns may become powerful biomarkers for diagnosis and prognosis of HNOC. In addition, microRNA therapy could be a novel strategy for HNOC prevention and therapeutics. Recent advances in microRNA expression profiling have led to a better understanding of the cancer pathogenesis. In this review, we will survey recent technological advances in microRNA profiling and their applications in defining microRNA markers/targets for cancer prediction, diagnostics, treatment, and prognostics. MicroRNA alterations that consistently identified in HNOC will be discussed, such as upregulation of miR-21, miR-31, miR-155, and downregulation of miR-26b, miR-107, miR-133b, miR-138, and miR-139. Copyright (C) 2009 Xiqiang Liu et al.
引用
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页数:11
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