MicroRNA gene expression deregulation in human breast cancer

被引:3306
作者
Iorio, MV
Ferracin, M
Liu, CG
Veronese, A
Spizzo, R
Sabbioni, S
Magri, E
Pedriali, M
Fabbri, M
Campiglio, M
Ménard, S
Palazzo, JP
Rosenberg, A
Musiani, P
Volinia, S
Nenci, I
Calin, GA
Querzoli, P
Negrini, M
Croce, CM
机构
[1] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA
[2] Univ Ferrara, Dipartimento Med Sperimentale & Diagnost, I-44100 Ferrara, Italy
[3] Univ Ferrara, Ctr Interdipattimentale Ric Canc, I-44100 Ferrara, Italy
[4] Ist Nazl Tumori, Dept Expt Oncol, Mol Targeting Unit, I-20133 Milan, Italy
[5] Thomas Jefferson Univ, Dept Pathol, Philadelphia, PA 19107 USA
[6] Thomas Jefferson Univ, Dept Anat & Cell Biol, Philadelphia, PA 19107 USA
[7] Thomas Jefferson Univ, Dept Surg, Philadelphia, PA 19107 USA
[8] CeSI Aging Res Ctr, Chieti, Italy
关键词
D O I
10.1158/0008-5472.CAN-05-1783
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are a class of small noncoding RNAs that control gene expression by targeting mRNAs and triggering either translation repression or RNA degradation. Their aberrant expression may be involved in human diseases, including cancer. Indeed, miRNA aberrant expression has been previously found in human chronic lymphocytic leukemias, where miRNA signatures were associated with specific clinicobiological features. Here, we show that, compared with normal breast tissue, miRNAs are also aberrantly expressed in human breast cancer. The overall miRNA expression could clearly separate normal versus cancer tissues, with the most significantly deregulated miRNAs being mir-125b, mir-145, mir-21, and mir-155. Results were confirmed by microarray and Northern blot analyses. We could identify miRNAs whose expression was correlated with specific breast cancer biopathologic features, such as estrogen and progesterone receptor expression, tumor stage, vascular invasion, or proliferation index.
引用
收藏
页码:7065 / 7070
页数:6
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