MicroRNA-126 inhibits invasion in non-small cell lung carcinoma cell lines

被引:281
作者
Crawford, M. [1 ]
Brawner, E. [1 ]
Batte, K. [1 ]
Yu, L. [2 ]
Hunter, M. G. [1 ]
Otterson, G. A. [3 ]
Nuovo, G. [1 ]
Marsh, C. B. [1 ]
Nana-Sinkam, S. P. [1 ]
机构
[1] Ohio State Univ, Med Ctr, Div Pulm Allergy Crit Care & Sleep Med, Columbus, OH 43210 USA
[2] Ohio State Univ, Ctr Biostat, Columbus, OH 43210 USA
[3] Ohio State Univ, Med Ctr, Div Hematol & Oncol, Columbus, OH 43210 USA
关键词
lung cancer; Crk; MicroRNA; invasion; adhesion;
D O I
10.1016/j.bbrc.2008.06.090
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
Crk is a member of a family of adaptor proteins that are involved in intracellular signal pathways altering cell adhesion, proliferation, and migration. Increased expression of Crk has been described in lung cancer and associated with increased tumor invasiveness. MicroRNAs (miRNAs) are a family of small non-coding RNAs (approximately 21-25 nt long) that are capable of targeting genes for either degradation of mRNA or inhibition of translation. Crk is a predicted putative target gene for miR-126. Over-expression of miR126 in a lung cancer cell line resulted in a decrease in Crk protein without any alteration in the associated mRNA. These lung cancer cells exhibit a decrease in adhesion, migration, and invasion. Decreased cancer cell invasion was also evident following targeted knockdown of Crk. MiR-126 alters lung cancer cell phenotype by inhibiting adhesion, migration, and invasion and the effects on invasion may be partially mediated through Crk regulation. (c) 2008 Elsevier Inc. All Fights reserved.
引用
收藏
页码:607 / 612
页数:6
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