MicroRNA analysis of microdissected normal squamous esophageal epithelium and tumor cells

被引:2
作者
Zhu, Liang [1 ]
Yan, Wusheng [1 ]
Rodriguez-Canales, Jaime [1 ]
Rosenberg, Alex M. [1 ]
Hu, Nan [2 ]
Goldstein, Alisa M. [2 ]
Taylor, Philip R. [2 ]
Erickson, Heidi S. [3 ]
Emmert-Buck, Michael R. [1 ]
Tangrea, Michael A. [1 ]
机构
[1] Ctr Canc Res, Pathol Lab, Pathogenet Unit, Bethesda, MD USA
[2] NCI, Genet Epidemiol Branch, Div Canc Epidemiol & Genet, NIH, Bethesda, MD 20892 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Esophageal squamous cell carcinoma; laser capture microdissection; microRNA; basal layer; differentiated layer; miR-25; miR-106b; miR-21; miR-203; miR-145; GENE-EXPRESSION; LASER-CAPTURE; BARRETTS-ESOPHAGUS; CANCER STATISTICS; SUPPRESSOR GENE; PROFILES; CARCINOMA; TARGETS; SIGNATURES; INVASION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies have identified several dysregulated microRNAs in esophageal squamous cell carcinoma (ESCC); however, to date there are no ex vivo analyses comparing expression levels of these regulatory molecules in esophageal squamous cell tumors versus patient-matched normal epithelium. We describe here a technical strategy to evaluate microRNAs in normal esophageal basal cells (NB), normal esophageal differentiated cells (ND), and tumor cells (T). Laser capture microdissection was used to procure target populations from five cases and 18 ESCC-associated microRNAs were measured by RT-qPCR. Five microRNAs (miR-25, miR-106b, miR-21, miR-203, and miR-145) demonstrated consistent differential expression in at least one of the three comparisons: T vs. NB, T vs. ND, or NB vs. ND. The potential regulatory role of the microRNAs in ESCC was further evaluated by correlating their expression with a matched mRNA dataset, which included the same five cases and cell populations. In conclusion, the present work demonstrates the feasibility of studying microRNA levels in precisely dissected cell populations from clinical samples, and sheds light on the molecular mechanisms associated with ESCC.
引用
收藏
页码:574 / 584
页数:11
相关论文
共 87 条
[1]  
[Anonymous], J BIOL CHEM
[2]   MicroRNA-21 (miR-21) post-transcriptionally downregulates tumor suppressor Pdcd4 and stimulates invasion, intravasation and metastasis in colorectal cancer [J].
Asangani, I. A. ;
Rasheed, S. A. K. ;
Nikolova, D. A. ;
Leupold, J. H. ;
Colburn, N. H. ;
Post, S. ;
Allgayer, H. .
ONCOGENE, 2008, 27 (15) :2128-2136
[3]   MicroRNA signature in massive macronodular adrenocortical disease and implications for adrenocortical tumourigenesis [J].
Bimpaki, Eirini I. ;
Iliopoulos, Dimitrios ;
Moraitis, Andreas ;
Stratakis, Constantine A. .
CLINICAL ENDOCRINOLOGY, 2010, 72 (06) :744-751
[4]  
BIRKS DK, 2010, PEDIAT BLOOD CANC
[5]   CLONING AND CHARACTERIZATION OF A RNASE-L INHIBITOR - A NEW COMPONENT OF THE INTERFERON-REGULATED 2-5A PATHWAY [J].
BISBAL, C ;
MARTINAND, C ;
SILHOL, M ;
LEBLEU, B ;
SALEHZADA, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (22) :13308-13317
[6]   Multiple E2F-Induced MicroRNAs Prevent Replicative Stress in Response to Mitogenic Signaling [J].
Bueno, Maria J. ;
Gomez de Cedron, Marta ;
Laresgoiti, Usua ;
Fernandez-Piqueras, Jose ;
Zubiaga, Ana M. ;
Malumbres, Marcos .
MOLECULAR AND CELLULAR BIOLOGY, 2010, 30 (12) :2983-2995
[7]   MicroRNA-21 in Cardiovascular Disease [J].
Cheng, Yunhui ;
Zhang, Chunxiang .
JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2010, 3 (03) :251-255
[8]  
CHIANG Y, 2010, J GASTROINTEST SURG
[9]   miRNA expression profiling of lung adenocarcinomas: correlation with mutational status [J].
Dacic, Sanja ;
Kelly, Lindsey ;
Shuai, Yongli ;
Nikiforova, Marina N. .
MODERN PATHOLOGY, 2010, 23 (12) :1577-1582