Identification of miR-601 as a novel regulator in the development of pancreatic cancer

被引:21
作者
Cao, Wenxi [1 ]
Jin, Huihan [2 ]
Zhang, Lei [2 ]
Chen, Xiao [2 ]
Qian, Haixin [1 ]
机构
[1] Suzhou Univ, Affiliated Hosp 1, Dept Gen Surg, 296 Shizi Rd, Suzhou 215006, Peoples R China
[2] Wuxi 2 Peoples Hosp, Dept Heptabiliary Surg, 68 Zhongshan Rd, Wuxi 214001, Peoples R China
关键词
Pancreatic cancer; miR-601; SIRT1; EPITHELIAL-MESENCHYMAL TRANSITION; SERUM MICRORNAS; INVASION; INSIGHTS;
D O I
10.1016/j.bbrc.2016.12.090
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Pancreatic cancer (PC) is one of the most aggressive malignancies, with a high mortality. Distant metastasis and recurrence are the main causes of PC-related deaths. MicroRNAs (miRNAs) have been reported in the serum or tumor tissue of cancer patients, including PC, which makes them potential biomarkers. The dysfunction of many miRNAs has been linked to PC occurrence and metastasis. In the current study, we found that miR-601 expression was significantly lower in PC samples, especially in metastatic compared to non-metastatic PC tissues. Gain-of-function and loss-of-function analysis showed that miR-601 suppressed PC cell proliferation and migration. One potential mechanism is that miR-601 inhibited the expression of Sirtuin 1 (SIRT1), which is a well-known regulator of PC development. We found that overexpression of SIRT1 could reverse the effect of miR-601 on PC cells. Our investigation therefore suggests that both miR-601 and SIRT1 are possible biomarkers for the early detection, and targets for the treatment of PC. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:638 / 644
页数:7
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