PER3, a novel target of miR-103, plays a suppressive role in colorectal cancer in vitro

被引:46
|
作者
Hong, Zhang [1 ]
Feng, Zhang [2 ]
Sai, Zhang [3 ]
Tao, Su [3 ]
机构
[1] Cent South Univ, Xiangya Hosp, Nurse Dept Organ Transplantat, Changsha 41008, Hunan, Peoples R China
[2] Cent South Univ, Xiangya Sch Med, Changsha 41008, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp, Inst Med Sci, Changsha 41008, Hunan, Peoples R China
关键词
Circadian clock gene; Colorectal cancer; miR-103; Period3; Vitro; CIRCADIAN CLOCK; INVASION; METASTASIS; EXPRESSION; P53;
D O I
10.5483/BMBRep.2014.47.9.212
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
Colorectal cancer has become the third most common cancer and leads to high mortality worldwide. Although colorectal cancer has been studied widely, the underlying molecular mechanism remains unclear. PER3 is related to tumor differentiation and the progression of colorectal cancer. High expression of miR-103 is associated with poor prognosis in patients with colorectal cancer. However, the relationship between miR-103 and PER3 in CRC cells remains unclear. In this study, we found that PER3 was downregulated in CRC tissues and CRC cell lines, whereas miR-103 was upregulated in CRC cell lines. We also found that PER3 promoted CRC cells apoptosis. These results indicate that PER3 plays a suppressive role in CRC cells. Moreover, we found that PER3 was targeted, at least partially, by miR-103. Taken together, we provide evidence to characterize the role of PER3 in CRC, which may be a new therapeutic target for CRC.
引用
收藏
页码:500 / 505
页数:6
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