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Abstract:
The expression of miR-203 has been reported to be significantly down-regulated in esophageal cancer. We showed here that overexpression of miR-203 in esophageal cancer cells dramatically increased cell apoptosis and inhibited cell proliferation, migration and invasion as well as tumor growth and down-regulated miR-21 expression. We subsequently identified that small GTPase Ran was a target gene of miR-203. Furthermore, Ran restoration partially counteracted the tumor suppressive effects of miR-203 and increased miR-21 expression. Taken together, our findings suggest that miR-203 may act as novel tumor suppressor in esophageal cancer through down-regulating the expression of Ran and miR-21. (C) 2013 Elsevier Ireland Ltd. Published by Elsevier Ltd. All rights reserved.
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CANCER LETTERS
ISSN: 0304-3835
Year: 2014
Issue: 1
Volume: 342
Page: 121-129
9 . 7 0 0
JCR@2022
ESI Discipline: CLINICAL MEDICINE;
ESI HC Threshold:222
JCR Journal Grade:1
CAS Journal Grade:2
Cited Count:
WoS CC Cited Count: 85
SCOPUS Cited Count: 88
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 6
Affiliated Colleges: