MicroRNA 133B targets pro-survival molecules MCL-1 and BCL2L2 in lung cancer

被引:162
作者
Crawford, Melissa [1 ]
Batte, Kara [1 ]
Yu, Lianbo [2 ]
Wu, Xin [3 ]
Nuovo, Gerard J. [4 ]
Marsh, Clay B. [1 ]
Otterson, Gregory A. [3 ]
Nana-Sinkam, Serge P. [1 ]
机构
[1] DHLRI, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Biostat, Columbus, OH 43210 USA
[3] Div Hematol & Oncol, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
MicroRNA; Apoptosis; Lung cancer; Chemotherapy; BCL2; MCL-1; REAL-TIME PCR; SQUAMOUS-CELL CARCINOMA; DOWN-REGULATION; APOPTOSIS; GENES; EXPRESSION; RESISTANCE; IDENTIFICATION; GEMCITABINE; SIGNATURES;
D O I
10.1016/j.bbrc.2009.07.143
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
Lung cancer is the most frequent cause of cancer-related death in this country for men and women. MicroRNAs ( miRNAs) are a family of small non-coding RNAs ( approximately 21-25 nt long) capable of targeting genes for either degradation of mRNA or inhibition of translation. We identified aberrant expression of 41 miRNAs in lung tumor versus uninvolved tissue. MiR-133B had the lowest expression of miRNA in lung tumor tissue (28-fold reduction) compared to adjacent uninvolved tissue. We identified two members of the BCL-2 family of pro-survival molecules (MCL-1 and BCL2L2 (BCLw)) as predicted targets of miR-133B. Selective over-expression of miR-133B in adenocarcinoma (H2009) cell lines resulted in reduced expression of both MCL-1 and BCL2L2. We then confirmed that miR-133B directly targets the 3'UTRs of both MCL-1 and BCL2L2. Lastly, over-expression of miR-133B induced apoptosis following gemcitabine exposure in these tumor cells. To our knowledge, this represents the first observation of decreased expression of miR-133B in lung cancer and that it functionally targets members of the BCL-2 family. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:483 / 489
页数:7
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