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2000
Volume 14, Issue 10
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

Objective: To explore the function of p42.3 in gastric carcinoma. Methods: We summarized the intricate regulation of p42.3 in gastric carcinoma from several aspects, namely, the structure features, the expression level, its regulation on cell cycle and EMT, its relationship with miR-29a as well as the optimal feedback circuit involved in. Results: We addressed the complex functions of p42.3 in regulating EMT, migration, invasion, proliferation and the optimal regulation network in GC, as well as the significant up/down-stream signal molecules involved in the pathway. We have also illuminated that miR-29a can inhibit cell proliferation and block the cell cycle, at least in part, via the repression of p42.3. Conclusion: In short, p42.3 might serve as a potential therapeutic target in the treatment of GC.

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/content/journals/lddd/10.2174/1570180814666170306121357
2017-10-01
2025-07-03
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/content/journals/lddd/10.2174/1570180814666170306121357
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  • Article Type:
    Research Article
Keyword(s): cell cycle; EMT; gastric carcinoma; miR-29a; p42.3; therapeutic target
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