A polycistronic microRNA cluster, miR-17-92, is overexpressed in human lung cancers and enhances cell proliferation

被引:1027
作者
Hayashita, Y
Osada, H
Tatematsu, Y
Yamada, H
Yanagisawa, K
Tomida, S
Yatabe, Y
Kawahara, K
Sekido, Y
Takahashi, T
机构
[1] Nagoya Univ, Grad Sch Med, Div Mol Carcinogenesis, Ctr Neurol Dis & Canc,Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Aichi Canc Ctr, Res Inst, Div Mol Oncol, Nagoya, Aichi 464, Japan
[3] Aichi Canc Ctr Hosp, Dept Anat Pathol, Nagoya, Aichi 464, Japan
[4] Aichi Canc Ctr Hosp, Dept Mol Diagnost Pathol, Nagoya, Aichi 464, Japan
[5] Oita Univ, Fac Med, Dept Oncol Sci Surg 2, Oita 87011, Japan
关键词
D O I
10.1158/0008-5472.CAN-05-2352
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small noncoding RNAs, thought to be involved in physiologic and developmental processes by negatively regulating expression of target genes. We have previously reported frequent down-regulation of the let-7 miRNA family in lung cancers and, in the present study, assessed alteration in a panel of 19 lung cancer cell lines. As a result, we found for the first time that the miR-17-92 cluster, which comprises seven miRNAs and resides in intron 3 of the C13orf25 gene at 13q31.3, is markedly overexpressed in lung cancers, especially with small-cell lung cancer histology. Southern blot analysis revealed the presence of increased gene copy numbers of the miRNA cluster in a fraction of lung cancer cell lines with overexpression. In addition, we were able to show predominant localization of C13orf25 transcripts within the nucleus and introduction of the expression construct of the miR-17-92 cluster, but not the putative open reading frame of C13orf25, enhancing lung cancer cell growth. These findings clearly suggest that marked overexpression of the miR-17-92 cluster with occasional gene amplification may play a role in the development of lung cancers, especially in their most aggressive form, small-cell lung cancer, and that the C13orf25 gene may well be serving as a vehicle in this regard.
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页码:9628 / 9632
页数:5
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