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摘要:
Dysregulation of miR-203-3p and miR-21-5p has been identified in esophageal cancer (EC). The restoration of miR-203-3p and reduction of miR-21-5p were able to cause tumor suppression. Here, co-transfection of miR-203-3p mimics and miR-21-5p inhibitors led to an extraordinary increased expression of miR-203-3p and synergistically inhibited proliferation, migration, and invasion in EC cells. Moreover, we found that Ran GTPase (Ran) was dramatically inhibited in EC cells treated with the co-transfection of miR-203-3p mimics and miR-21-5p inhibitors. Finally, in-vivo studies showed that overexpression of miR-203-3p, combined with the suppression of miR-21-5p, significantly co-inhibited growth of tumors. The obtained data suggested that the development of miRNA-based combination therapeutics represents a promising cancer treatment strategy. Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved.
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ANTI-CANCER DRUGS
ISSN: 0959-4973
年份: 2019
期: 1
卷: 30
页码: 38-45
2 . 3 0 0
JCR@2022
ESI学科: PHARMACOLOGY & TOXICOLOGY;
ESI高被引阀值:122
JCR分区:4