MUC1 Regulates Expression of Multiple microRNAs Involved in Pancreatic Tumor Progression, Including the miR-200c/141 Cluster

被引:29
|
作者
Mohr, Ashley M. [1 ]
Bailey, Jennifer M. [2 ]
Lewallen, Michelle E. [3 ]
Liu, Xiang [1 ]
Radhakrishnan, Prakash [1 ]
Yu, Fang [4 ]
Tapprich, William [5 ]
Hollingsworth, Michael A. [1 ]
机构
[1] Univ Nebraska Med Ctr, Eppley Inst Res Canc & Allied Dis, Omaha, NE USA
[2] Johns Hopkins Univ, Sch Med, Dept Surg, Sol Goldman Pancreat Canc Res Ctr, Baltimore, MD 21205 USA
[3] Stowers Inst Med Res, Kansas City, MO USA
[4] Univ Nebraska Med Ctr, Coll Publ Hlth Biostat, Omaha, NE USA
[5] Univ Nebraska, Dept Biol, Omaha, NE 68182 USA
来源
PLOS ONE | 2013年 / 8卷 / 10期
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; CELL LUNG-CANCER; BETA-CATENIN; E-CADHERIN; DOWN-REGULATION; TARGETING ZEB1; C-SRC; TRANSCRIPTION; GROWTH; CARCINOMA;
D O I
10.1371/journal.pone.0073306
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
MUC1 is a transmembrane glycoprotein that modulates transcription via its cytoplasmic domain. We evaluated the capacity of MUC1 to regulate the global transcription of microRNAs in pancreatic cancer cells expressing MUC1. Results indicated that MUC1 regulated expression of at least 103 microRNAs. We evaluated further regulation of the microRNA transcript cluster miR-200c/141, which was among the most highly regulated microRNAs. We found that MUC1 directly interacted with ZEB1, a known transcriptional repressor of the miR-200c/141 cluster, at the promoter of miR-200c/141, and further reduced transcript production. These data indicate that signaling through MUC1 influences cancer progression by regulating transcription of microRNAs that are associated with the process of metastasis.
引用
收藏
页数:13
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