let-7 microRNA functions as a potential growth suppressor in human colon cancer cells

被引:512
作者
Akao, Yukihiro
Nakagawa, Yoshihito
Naoe, Tomoki
机构
[1] Gifu Int Inst Biotechnol, Dept Genet Diag, Gifu 5040838, Japan
[2] Nagoya Univ, Grad Sch Med, Dept Hematol, Showa Ku, Nagoya, Aichi 4668550, Japan
关键词
microRNA; let-7; colon cancer; RAS; growth inhibition;
D O I
10.1248/bpb.29.903
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNAs (miRNAs) are endogenously expressed RNAs, 18-25 nucleotides in length, that repress protein translation through binding to target mRNAs. miRNAs have been implicated in many cellular processes including cell proliferation, differentiation, and death. Recently, let-7 miRNAs were found to regulate human RAS oncogene expression and to be often down-regulated in human lung tumors. In this study, we examined the expression of let-7 miRNAs in human colon cancer tumors and cell lines, with the result that 2 of 6 cases and 1 of 3 cell lines showed reduced expression of let-7. When let-7 low-expressing DLD-1 human colon cancer cells were transfected with let-7a-1 precursor miRNA, which is located at chromosome 9q22.3, the cells underwent significant growth suppression. At that time, the levels of RAS and c-myc proteins were lowered after the transfection, whereas the levels of both of their mRNAs remained almost unchanged. These findings suggest the involvement of let-7 miRNA in the growth of colon cancer cells. Thus, miRNAs might provide a basis for novel RNA anti-cancer agents.
引用
收藏
页码:903 / 906
页数:4
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