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Keywords {🔍}

resveratrol, cells, lovo, cancer, ecadherin, expression, emt, tgfβ, article, pubmed, invasion, snail, cell, google, scholar, figure, signaling, pathway, colorectal, cas, inhibit, metastasis, treatment, transition, migration, crc, mice, metastases, lung, tgfβinduced, vimentin, inhibited, transcription, shanghai, compared, treated, effect, vivo, metastatic, results, ability, mgkg, group, tumor, lesions, epithelial, mesenchymal, promoter, mrna, factors,

Topics {✒️}

recombinant plasmid pgl3-basic-e-cadherin transforming growth factor-beta tgf-β1/smads signaling pathway tgf-β/smads signaling pathway tgf-β-induced epithelial-mesenchymal transition tgf-β/smad signaling pathway contributed reagents/materials/analysis tools suppressing tgf-β1-induced emt tgf-β1-induced emt promoted inhibited tgf-β1-induced emt tgfβ/smad signaling pathway long-term basic research open access license smads signaling pathway inhibit tgf-β1-induced emt 10 ng/ml tgf-β1 tgf-βri/tgf-βrii tgf-β/smad2/3 pathway death-inducing signaling complex tgf-β1-induced emt tgf-β1 induced emt basic-mut-e-cadherin tgf-β-induced emt hrp-conjugated secondary antibodies tubular epithelial-mesenchymal transition phosphorylating cell-surface receptors article download pdf e-cadherin rabbit antibody e-cadherin epithelial markers tgfbeta family signalling e-cadherin changed consistently e-cadherin decreased obviouslywhile emt-induced trascription factors dual-luciferase assay kit effective anti-cancer activity tgf-β induced decreased e-cadherin transcription e-cadherin mrna expression cell-cell adhesion lovo-plv4-gfp cells emt-induced transcription factors resveratrol downregulates akt/gsk a549 cell line cell signaling technology mesenchymal transition induced resveratrol suppresses epithelial e-cadherin induced colorectal cancer including epithelial-mesenchymal transition adding tgf-β1

Schema {🗺️}

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         headline:Resveratrol suppresses epithelial-to-mesenchymal transition in colorectal cancer through TGF-β1/Smads signaling pathway mediated Snail/E-cadherin expression
         description:Resveratrol extracted from grape has been an ideal alternative drug in the therapy of different cancers including colorectal cancer (CRC). Since the underlying mechanisms of resveratrol on the invasion and metastasis of CRC have not been fully elucidated, and epithelial-to-mesenchymal transition (EMT) is a key process associated with the progression of CRC, here we aimed to investigate the potential mechanism of resveratrol on the inhibition of TGF-β1-induced EMT in CRC LoVo cells. We investigated the anticancer effect of resveratrol against LoVo cells in vitro and in vivo. In vivo, the impact of resveratrol on invasion and metastasis was investigated by mice tail vein injection model and mice orthotopic transplantation tumor model. In vivo imaging was applied to observe the lungs metastases, and hemaoxylin-eosin (HE) staining was used to evaluate metastatic lesions. In vitro, impact of resveratrol on the migration and invasion of LoVo cells was evaluated by transwell assay. Inhibition effect of resveratrol on TGF-β-induced EMT was examined by morphological observation. Epithelial phenotype marker E-cadherin and mesenchymal phenotype marker Vimentin were detected by western blot and immunofluorescence. Promoter activity of E-cadherin was measured using a dual-luciferase assay kit. mRNA expression of Snail and E-cadherin was measured by RT-PCR. We demonstrated that, resveratrol inhibited the lung metastases of LoVo cells in vivo. In addition, resveratrol reduced the rate of lung metastases and hepatic metastases in mice orthotopic transplantation. In vitro, TGF-β1-induced EMT promoted the invasion and metastasis of CRC, reduced the E-cadherin expression and elevated the Vimentin expression, and activated the TGF-β1/Smads signaling pathway. But resveratrol could inhibit the invasive and migratory ability of LoVo cells in a concentration-dependent manner, increase the expression of E-cadherin, repress the expression of Vimentin, as well as the inhibition of TGF-β1/Smads signaling pathway. Meanwhile, resveratrol reduced the level of EMT-inducing transcription factors Snail and the transcription of E-cadherin during the initiation of TGF-β1-induced EMT. Our new findings provided evidence that, resveratrol could inhibit EMT in CRC through TGF-β1/Smads signaling pathway mediated Snail/E-cadherin expression, and this might the potential mechanism of resveratrol on the inhibition of invasion and metastases in CRC.
         datePublished:2015-03-05T00:00:00Z
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            Colorectal cancer
            Epithelial-to-mesenchymal transition
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            Cancer Research
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      headline:Resveratrol suppresses epithelial-to-mesenchymal transition in colorectal cancer through TGF-β1/Smads signaling pathway mediated Snail/E-cadherin expression
      description:Resveratrol extracted from grape has been an ideal alternative drug in the therapy of different cancers including colorectal cancer (CRC). Since the underlying mechanisms of resveratrol on the invasion and metastasis of CRC have not been fully elucidated, and epithelial-to-mesenchymal transition (EMT) is a key process associated with the progression of CRC, here we aimed to investigate the potential mechanism of resveratrol on the inhibition of TGF-β1-induced EMT in CRC LoVo cells. We investigated the anticancer effect of resveratrol against LoVo cells in vitro and in vivo. In vivo, the impact of resveratrol on invasion and metastasis was investigated by mice tail vein injection model and mice orthotopic transplantation tumor model. In vivo imaging was applied to observe the lungs metastases, and hemaoxylin-eosin (HE) staining was used to evaluate metastatic lesions. In vitro, impact of resveratrol on the migration and invasion of LoVo cells was evaluated by transwell assay. Inhibition effect of resveratrol on TGF-β-induced EMT was examined by morphological observation. Epithelial phenotype marker E-cadherin and mesenchymal phenotype marker Vimentin were detected by western blot and immunofluorescence. Promoter activity of E-cadherin was measured using a dual-luciferase assay kit. mRNA expression of Snail and E-cadherin was measured by RT-PCR. We demonstrated that, resveratrol inhibited the lung metastases of LoVo cells in vivo. In addition, resveratrol reduced the rate of lung metastases and hepatic metastases in mice orthotopic transplantation. In vitro, TGF-β1-induced EMT promoted the invasion and metastasis of CRC, reduced the E-cadherin expression and elevated the Vimentin expression, and activated the TGF-β1/Smads signaling pathway. But resveratrol could inhibit the invasive and migratory ability of LoVo cells in a concentration-dependent manner, increase the expression of E-cadherin, repress the expression of Vimentin, as well as the inhibition of TGF-β1/Smads signaling pathway. Meanwhile, resveratrol reduced the level of EMT-inducing transcription factors Snail and the transcription of E-cadherin during the initiation of TGF-β1-induced EMT. Our new findings provided evidence that, resveratrol could inhibit EMT in CRC through TGF-β1/Smads signaling pathway mediated Snail/E-cadherin expression, and this might the potential mechanism of resveratrol on the inhibition of invasion and metastases in CRC.
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      dateModified:2015-03-05T00:00:00Z
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         Resveratrol
         Colorectal cancer
         Epithelial-to-mesenchymal transition
         TGF-β1/Smads signaling pathway
         Snail
         E-cadherin
         Cancer Research
         Oncology
         Surgical Oncology
         Health Promotion and Disease Prevention
         Biomedicine
         general
         Medicine/Public Health
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      name:Linlin Yan
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            name:Shanghai University of Traditional Chinese Medicine
            address:
               name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
               type:PostalAddress
            type:Organization
      name:Haili Jiang
      affiliation:
            name:Shanghai University of Traditional Chinese Medicine
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      name:Jianlin Ren
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            address:
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               type:PostalAddress
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      name:Jianfeng Cai
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      name:Qi Li
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      name:Research Center for Traditional Chinese Medicine and Systems Biology, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China
      name:Shanghai Municipal Hospital of Traditional Chinese Medicine, Department of Oncology, Shanghai, China
      name:Department of Chemistry, University of South Florida, Tampa, USA
      name:Department of Medical Oncology, Shuguang Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China

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