LincRNA-RoR/miR-145 promote invasion and metastasis in triple-negative breast cancer via targeting MUC1

被引:47
作者
Ma, Jianli [1 ]
Yang, Yue [2 ]
Huo, Desheng [3 ]
Wang, Zanyu [4 ]
Zhai, Xiaoyu [5 ]
Chen, Jing [6 ]
Sun, Huixin [2 ]
An, Weiwei [2 ]
Jie, Jing [5 ]
Yang, Pengxiang [2 ,7 ,8 ]
机构
[1] Harbin Med Univ Canc Hosp, Dept Radiat Oncol, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Heilongjiang Acad Med Sci, Inst Canc Prevent & Treatment, Harbin 150081, Heilongjiang, Peoples R China
[3] Jilin Univ, Coll Basic Med Sci, Dept Histol & Embryol, Changchun 130021, Jilin, Peoples R China
[4] Heilongjiang Vet Drug & Feed Supervis Inst, Harbin 150040, Heilongjiang, Peoples R China
[5] Jilin Univ, Dept Immunol, Coll Basic Med Sci, Changchun 130021, Jilin, Peoples R China
[6] Tianjin Med Univ Canc Inst & Hosp, Natl Clin Res Ctr Canc, Key Lab Canc Prevent & Therapy, Dept Pancreat Canc, Tianjin 300060, Peoples R China
[7] Chinese Acad Med Sci, Inst Biomed Engn, Tianjin Key Lab Biomat Res, Tianjin 300192, Peoples R China
[8] Peking Union Med Coll, Tianjin 300192, Peoples R China
关键词
LincRNA-ROR; Triple-negative breast cancer; Invasion and metastasis; MUC1; NONCODING RNAS; ROR PROMOTES; LINCRNA-ROR; PANCREATIC-CANCER; RESISTANCE; CELLS;
D O I
10.1016/j.bbrc.2018.04.119
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
Triple-negative breast cancer (TNBC) was associated with high rates of cancer recurrence and metastasis and currently no available molecularly target. Accumulating evidences have established the importance of lincRNA-ROR as a marker of cancers. In order to better understand the mechanism of lincRNA-ROR in TNBC, we provided a novel molecular target into the regulatory invasion and metastasis in present research. We found that lincRNA-ROR was upregulated in TNBC cell lines and tissue samples. The aberrant expression of lincRNA-ROR was shown to increase invasion and metastasis in MDA-MB-231 and loss of function by siRNA reverse these process. Furthermore, lincRNA-ROR functions as a competing endogenous RNAs (ceRNA) which sponges miR-145 and therefore upregulate the expression of Mucin1 (MUC1). The expression of MUC1 impacted E-cadherin membrane localization. Together, MUC1 was a potential molecular target may help explain the role of lincRNA-ROR/miR-145 for invasion and metastasis in TNBC cell lines. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:614 / 620
页数:7
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