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MicroRNA-375 Is Downregulated in Gastric Carcinomas and Regulates Cell Survival by Targeting PDK1 and 14-3-3ζ
被引:379
作者:
Tsukamoto, Yoshiyuki
[1
]
Nakada, Chisato
[1
]
Noguchi, Tsuyoshi
[2
]
Tanigawa, Masato
[4
]
Lam Tung Nguyen
[1
,3
]
Uchida, Tomohisa
[1
]
Hijiya, Naoki
[1
]
Matsuura, Keiko
[1
]
Fujioka, Toshio
[3
]
Seto, Masao
[5
]
Moriyama, Masatsugu
[1
]
机构:
[1] Oita Univ, Dept Mol Pathol, Fac Med, Yufu City, Oita 8795593, Japan
[2] Oita Univ, Dept Gastrointestinal Surg, Fac Med, Yufu City, Oita 8795593, Japan
[3] Oita Univ, Dept Gastroenterol, Fac Med, Yufu City, Oita 8795593, Japan
[4] Oita Univ, Inst Sci Res, Yufu City, Oita 8795593, Japan
[5] Aichi Canc Ctr, Res Inst, Div Mol Med, Nagoya, Aichi 464, Japan
关键词:
COPY NUMBER ALTERATIONS;
GENE-EXPRESSION;
LUNG-CANCER;
APOPTOSIS;
AKT;
CLUSTER;
PLAYS;
PRINCIPLES;
MIR-17-92;
PATHWAY;
D O I:
10.1158/0008-5472.CAN-09-2777
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
We investigated expression profiles of microRNA (miRNA) in gastric carcinomas by use of a miRNA microarray platform covering a total of 470 human miRNAs. We identified 39 differentially expressed miRNAs in gastric carcinoma, of which six were significantly downregulated and the other 33 were upregulated. We found that miRNA-375 (miR-375) was the most downregulated and that its ectopic expression in gastric carcinoma cells markedly reduced cell viability via the caspase-mediated apoptosis pathway. Interestingly, we found that expression of miR-375 inhibited expression of PDK1, which is a direct target of miR-375, followed by suppression of Akt phosphorylation. Further analysis by gene expression microarray revealed that 14-3-3 zeta, a potent antiapoptotic gene, was significantly downregulated at both the mRNA and protein levels in cells transfected with miR-375. The activity of a luciferase reporter containing the miR-375 binding sequence at the 3' untranslated region (UTR) of 14-3-3 zeta mRNA was repressed by the ectopic expression of miR-375, suggesting that miR-375 targets the 3' UTR of 14-3-3 zeta. In addition, knockdown of either PDK1 or 14-3-3 zeta in gastric carcinoma cells induced caspase activation, which was also observed in miR-375-transfected cells, suggesting that miR-375 may exert its proapoptotic function, at least in part, through the downregulation of PDK1 and 14-3-3 zeta. Taken together, we propose that miR-375 is a candidate tumor suppressor miRNA in gastric carcinoma. Cancer Res; 70(6); 2339-49. (C) 2010 AACR.
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页码:2339 / 2349
页数:11
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