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      Down-Regulation of DDR1 Induces Apoptosis and Inhibits EMT through Phosphorylation of Pyk2/MKK7 in DU-145 and Lncap-FGC Prostate Cancer Cell Lines.

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          Abstract

          In cancer cells, re-activation of Epithelial-Mesenchymal Transition (EMT) program through Discoidin Domain Receptor1 (DDR1) leads to metastasis. DDR1-targeted therapy with siRNA might be a promising strategy for EMT inhibition. Therefore, the aim of this study was to investigate the effect of DDR1 knockdown in the EMT, migration, and apoptosis of prostate cancer cells. For this purpose, the expression of DDR1 was down regulated by the siRNA approach in LNcap-FGC and DU-145 prostate cancer cells.

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          Author and article information

          Journal
          Anticancer Agents Med Chem
          Anti-cancer agents in medicinal chemistry
          Bentham Science Publishers Ltd.
          1875-5992
          1871-5206
          2020
          : 20
          : 8
          Affiliations
          [1 ] Department of Clinical Biochemistry, School of Pharmacy & Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran.
          [2 ] Department of Clinical Biochemistry, Faculty of Medicine, Qom University of Medical Sciences, Qom, Iran.
          [3 ] Molecular and Medicine Research Center, Arak University of Medical Sciences, Arak, Iran.
          Article
          ACAMC-EPUB-105753
          10.2174/1871520620666200410075558
          32275493
          1dd37949-0d25-40ae-a5d7-5d981c0dcbdf
          History

          small interfering RNA,Pyk2,apoptosis,epithelial-mesenchymal transition (EMT),MKK7,Discoidin domain receptor 1 (DDR1)

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