MicroRNA let-7 downregulates STAT3 phosphorylation cancer cells by increasing SOCS3 expression

被引:60
|
作者
Patel, Kripa [1 ]
Kollory, Anita [1 ]
Takashima, Asami [1 ]
Sarkar, Sibaji [1 ]
Faller, Douglas V. [1 ]
Ghosh, Sajal K. [1 ]
机构
[1] Boston Univ, Sch Med, Ctr Canc, Boston, MA 02118 USA
关键词
Pancreatic cancer; STAT3; Let-7; SOCS3; EMT; EPITHELIAL-MESENCHYMAL TRANSITION; HISTONE DEACETYLASE INHIBITORS; EPIDERMAL-GROWTH-FACTOR; PANCREATIC-CANCER; SIGNAL TRANSDUCER; PHASE-III; GEMCITABINE; SUPPRESSOR; ACTIVATOR; PATHWAY;
D O I
10.1016/j.canlet.2014.01.020
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although dispensable for normal pancreatic function, STAT3 signaling is frequently activated in pancreatic cancers. Consistent downregulation of expression of microRNA let-7 is also characteristic of pancreatic ductal adenocarcinoma (PDAC) biopsy specimens. We demonstrate in this study that re-expression of let-7 in poorly-differentiated PDAC cell lines reduced phosphorylation/activation of STAT3 and its downstream signaling events and reduced the growth and migration of PDAC cells. Let-7 re-expression did not repress expression of STAT3 protein or its activator cytokine interleukin 6 (IL-6). However, let-7 re-expression enhanced cytoplasmic expression of suppressor of cytokine signaling 3 (SOCS3), which blocks STAT3 activation by JAK2. Our study thus identified a mechanism by which STAT3 signaling can be inhibited in pancreatic cancer cells by modifying let-7 expression. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:54 / 64
页数:11
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