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Identification of microRNA-487b as a negative regulator of liver metastasis by regulation of KRAS in colorectal cancer
被引:24
作者:
Hata, Tsuyoshi
[1
]
Mokutani, Yukako
[2
]
Takahashi, Hidekazu
[1
]
Inoue, Akira
[1
]
Munakata, Koji
[1
]
Nagata, Kazuya
[3
]
Haraguchi, Naotsugu
[1
]
Nishimura, Junichi
[1
]
Hata, Taishi
[1
]
Matsuda, Chu
[1
]
Murata, Kohei
[4
]
Mizushima, Tsunekazu
[1
]
Doki, Yuichiro
[1
]
Mori, Masaki
[1
]
Yamamoto, Hirofumi
[1
,3
]
机构:
[1] Osaka Univ, Grad Sch Med, Dept Surg Gastroenterol Surg, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Yao Municipal Hosp, Dept Surg, Yao, Osaka 5810069, Japan
[3] Osaka Univ, Grad Sch Med, Div Hlth Sci, Dept Mol Pathol, Suita, Osaka 5650871, Japan
[4] Suita Municipal Hosp, Dept Surg, Suita, Osaka 5640082, Japan
关键词:
miR-487b;
colorectal cancer;
liver metastasis;
KRAS;
LRP6;
MULTISTAGE CARCINOGENESIS;
HEPATOCELLULAR-CARCINOMA;
ACQUIRED-RESISTANCE;
CELL-PROLIFERATION;
BETA-CATENIN;
COLON-CANCER;
MUTANT KRAS;
LRP6;
PROMOTES;
EXPRESSION;
D O I:
10.3892/ijo.2016.3813
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Recent studies have shown that microRNAs (miRNAs) are involved in the progression of colorectal cancer (CRC). The aim of this study is to identify a novel miRNA that especially relates to liver metastasis and to explore the underlying mechanism. Differentially expressed miRNAs were analyzed using microarray, in primary CRC tumors without metastasis (n=16), those with liver metastasis (n=12), and liver metastatic lesions (n=8). We found that miR-487b level decreased in liver metastatic lesions, and qRT-PCR confirmed the results in the validating cohort (n=134). Survival analysis indicated that high expression of miR-487b was associated with better prognosis. In vitro studies were also performed to investigate the functional significance of miR-487b in human CRC cell lines. miR-487b showed an inhibitory effect on cell proliferation and invasion of CRC cells. miR-487b downregulated KRAS and inhibited its downstream signal pathways, and the luciferase reporter assay revealed that miR-487b directly targeted LRP6, a receptor for WNT/beta-catenin signaling. These findings showed that decrease in miR-487b was related with liver metastasis. Our data suggest a possibility that miR-487b may suppress metastasis of CRC progression through inhibition of KRAS.
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页码:487 / 496
页数:10
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