Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway

The epithelial-mesenchymal transition (EMT) is involved in neoplastic metastasis, and the RON protein may be involved. In the present study, we determined the role and the mechanisms of action of RON in EMT in Madin-Darby canine kidney (MDCK) cells by Western blot and cell migration analysis. Activa...

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Main Authors: Xu Xiangming, Qian Yun, Zhang Guoliang, Lin Jianjiang, Teng Lisong
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2011-07-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2011000700004&lng=en&tlng=en
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author Xu Xiangming
Qian Yun
Zhang Guoliang
Lin Jianjiang
Teng Lisong
author_facet Xu Xiangming
Qian Yun
Zhang Guoliang
Lin Jianjiang
Teng Lisong
author_sort Xu Xiangming
collection DOAJ
description The epithelial-mesenchymal transition (EMT) is involved in neoplastic metastasis, and the RON protein may be involved. In the present study, we determined the role and the mechanisms of action of RON in EMT in Madin-Darby canine kidney (MDCK) cells by Western blot and cell migration analysis. Activation of RON by macrophage stimulating protein (MSP) results in cell migration and initiates changes in the morphology of RON-cDNA-transfected MDCK cells. The absence of E-cadherin, the presence of vimentin and an increase in Snail were observed in RE7 cells, which were derived from MDCK cells transfected with wt-RON, compared with MDCK cells. Stimulation of RE7 cells with MSP resulted in increased migration (about 69% of the wounded areas were covered) as well as increased activation of extracellular signal-regulated kinase 1/2 (Erk1/2) and glycogen synthase kinase-3β (GSK-3β; the percent of the activation ratio was 143.6/599.8% and 512.4%, respectively), which could be inhibited with an individual chemical inhibitor PD98059 (50 μM) specific to MAPK/ERK kinase (the percent inhibition was 98.9 and 81.2%, respectively). Thus, the results indicated that RON protein could mediate EMT in MDCK cells via the Erk1/2 pathway. Furthermore, GSK-3β regulates the function of Snail in controlling EMT by this pathway.
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spelling doaj.art-24d5528fa3dc4d05bd201e5c989c042f2022-12-22T03:16:19ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2011-07-0144763464110.1590/S0100-879X2011000700004S0100-879X2011000700004Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathwayXu Xiangming0Qian Yun1Zhang Guoliang2Lin Jianjiang3Teng Lisong4Zhejiang UniversityZhejiang UniversityZhejiang UniversityZhejiang UniversityZhejiang UniversityThe epithelial-mesenchymal transition (EMT) is involved in neoplastic metastasis, and the RON protein may be involved. In the present study, we determined the role and the mechanisms of action of RON in EMT in Madin-Darby canine kidney (MDCK) cells by Western blot and cell migration analysis. Activation of RON by macrophage stimulating protein (MSP) results in cell migration and initiates changes in the morphology of RON-cDNA-transfected MDCK cells. The absence of E-cadherin, the presence of vimentin and an increase in Snail were observed in RE7 cells, which were derived from MDCK cells transfected with wt-RON, compared with MDCK cells. Stimulation of RE7 cells with MSP resulted in increased migration (about 69% of the wounded areas were covered) as well as increased activation of extracellular signal-regulated kinase 1/2 (Erk1/2) and glycogen synthase kinase-3β (GSK-3β; the percent of the activation ratio was 143.6/599.8% and 512.4%, respectively), which could be inhibited with an individual chemical inhibitor PD98059 (50 μM) specific to MAPK/ERK kinase (the percent inhibition was 98.9 and 81.2%, respectively). Thus, the results indicated that RON protein could mediate EMT in MDCK cells via the Erk1/2 pathway. Furthermore, GSK-3β regulates the function of Snail in controlling EMT by this pathway.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2011000700004&lng=en&tlng=enRONEpithelial-mesenchymal transitionMAPKErk
spellingShingle Xu Xiangming
Qian Yun
Zhang Guoliang
Lin Jianjiang
Teng Lisong
Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
Brazilian Journal of Medical and Biological Research
RON
Epithelial-mesenchymal transition
MAPK
Erk
title Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
title_full Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
title_fullStr Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
title_full_unstemmed Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
title_short Mechanisms of RON-mediated epithelial-mesenchymal transition in MDCK cells through the MAPK pathway
title_sort mechanisms of ron mediated epithelial mesenchymal transition in mdck cells through the mapk pathway
topic RON
Epithelial-mesenchymal transition
MAPK
Erk
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2011000700004&lng=en&tlng=en
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AT zhangguoliang mechanismsofronmediatedepithelialmesenchymaltransitioninmdckcellsthroughthemapkpathway
AT linjianjiang mechanismsofronmediatedepithelialmesenchymaltransitioninmdckcellsthroughthemapkpathway
AT tenglisong mechanismsofronmediatedepithelialmesenchymaltransitioninmdckcellsthroughthemapkpathway