The role of miR-766-5p in cell migration and invasion in colorectal cancer

被引:28
作者
Jia, Bin [1 ]
Xia, Lei [2 ]
Cao, Fang [2 ]
机构
[1] Shandong Univ Tradit Chinese Med, Affiliated Hosp, Dept Gastroenterol, Jinan 250014, Shandong, Peoples R China
[2] Shandong Univ Tradit Chinese Med, Affiliated Hosp, Dept Oncol, 16369 Jingshi Rd, Jinan 250014, Shandong, Peoples R China
关键词
colorectal cancer; suppressor of cancer cell invasion; miR-766-5p; MATRIX METALLOPROTEINASES; MICRORNAS; BIOMARKERS; TARGETS; ACTS;
D O I
10.3892/etm.2018.5716
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Colorectal cancer (CRC) develops from the colon or rectum and is the fourth highest inducer of cancer mortality. In the present study, cancer tissues and normal tissues were extracted from patients with CRC who were treated in the Affiliated Hospital of Shandong University of Traditional Chinese Medicine (Jinan, China). Reverse transcription-quantitative polymerase chain reaction demonstrated that the expression level of miR-766-5p was significantly higher (P<0.01) in cancer tissue than that in normal tissue. SW480 cells were used for in vitro study and randomly separated into the miR-negative control (NC) inhibitor treatment group and miR-766-5p inhibitor treatment group. SW480 cell behaviors were evaluated. Results demonstrated that in the miR-766-5p inhibitor group, there was a decreased level of cell proliferation/migration/invasion and higher cell apoptosis compared with that in the miR-NC inhibitor group. miR-766-5p was predicted and verified to target the 3' untranslated region of suppressor of cancer cell invasion (SCAI) in SW480 cells. Protein expression levels of matrix metalloproteinase-2/phosphoinositide 3-kinase/AKT were decreased and SCAI was increased following miR-766-5p inhibitor treatment. In conclusion, the present study indicated that miR-766-5p inhibitor repressed the process of CRC by targeting SCAI.
引用
收藏
页码:2569 / 2574
页数:6
相关论文
共 30 条
[1]   Physical Activity, Biomarkers, and Disease Outcomes in Cancer Survivors: A Systematic Review [J].
Ballard-Barbash, Rachel ;
Friedenreich, Christine M. ;
Courneya, Kerry S. ;
Siddiqi, Sameer M. ;
McTiernan, Anne ;
Alfano, Catherine M. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2012, 104 (11) :815-840
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   The role of the tissue microenvironment in the regulation of cancer cell motility and invasion [J].
Brabek, Jan ;
Mierke, Claudia T. ;
Roesel, Daniel ;
Vesely, Pavel ;
Fabry, Ben .
CELL COMMUNICATION AND SIGNALING, 2010, 8
[4]   SCAI acts as a suppressor of cancer cell invasion through the transcriptional control of β1-integrin [J].
Brandt, Dominique T. ;
Baarlink, Christian ;
Kitzing, Thomas M. ;
Kremmer, Elisabeth ;
Ivaska, Johanna ;
Nollau, Peter ;
Grosse, Robert .
NATURE CELL BIOLOGY, 2009, 11 (05) :557-U83
[5]  
Brody H, 2015, NATURE, V521, pS1, DOI [10.1038/521S1a, 10.1038/526S1a]
[6]   Targeting matrix metalloproteinases in cancer: Bringing new life to old ideas [J].
Cathcart, Jillian ;
Pulkoski-Gross, Ashleigh ;
Cao, Jian .
GENES & DISEASES, 2015, 2 (01) :26-34
[7]   Downregulation of SCAI enhances glioma cell invasion and stem cell like phenotype by activating Wnt/β-catenin signaling [J].
Chen, Xiangrong ;
Hu, Weipeng ;
Xie, Baoyuan ;
Gao, Hongzhi ;
Xu, Chaoyang ;
Chen, Junyan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 448 (02) :206-211
[8]   Modes of cancer cell invasion and the role of the microenvironment [J].
Clark, Andrew G. ;
Vignjevic, Danijela Matic .
CURRENT OPINION IN CELL BIOLOGY, 2015, 36 :13-22
[9]   Colorectal cancer [J].
Cunningham, David ;
Atkin, Wendy ;
Lenz, Heinz-Josef ;
Lynch, Henry T. ;
Minsky, Bruce ;
Nordlinger, Bernard ;
Starling, Naureen .
LANCET, 2010, 375 (9719) :1030-1047
[10]   Oncomirs - microRNAs with a role in cancer [J].
Esquela-Kerscher, A ;
Slack, FJ .
NATURE REVIEWS CANCER, 2006, 6 (04) :259-269