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We are analyzing https://link.springer.com/article/10.1007/s13277-015-4209-1.

Title:
Esculin and its oligomer fractions inhibit adhesion and migration of U87 glioblastoma cells and in vitro angiogenesis | Tumor Biology
Description:
Cancer metastasis is the major cause of cancer-related death. Chemoprevention is defined as the use of natural or synthetic substances to prevent cancer formation or cancer progress. In the present study, we investigate the antitumor activity of esculin and its oligomer fractions in U87 glioblastoma cells. We showed that esculin and its oligomers reduced U87 cell growth in a dose dependent manner. They also inhibited cell adhesion to collagen IV and vitronectin by interfering with the function of their respective receptors α2ÎČ1 and αvÎČ5 integrins. Furthermore, the tested samples were able to reduce migration of U87 cells towards another extracellular matrix fibronectin. Moreover, esculin and its oligomer fractions inhibited in vitro angiogenesis of endothelial cells (HMEC-1). In summary, our data provide the first evidence that esculin and its oligomer fractions are able to reduce adhesion, migration of glioblastoma cells and in vitro angiogenesis. Esculin and its oligomers may thus exert multi-target functions against cancer cells.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💾}

The income method remains a mystery to us.

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Keywords {🔍}

article, google, scholar, pubmed, cancer, cell, cells, cas, esculin, glioblastoma, angiogenesis, migration, activity, adhesion, coumarin, biol, chem, tumor, med, oligomer, fractions, vitro, res, privacy, cookies, content, mokdadbzeouich, ghedira, chekirghedira, matrix, access, oncol, lett, monastir, data, publish, research, search, ghoul, leila, integrins, effect, human, proliferation, evaluation, derivatives, bioorg, kim, université, information,

Topics {✒}

b16-f10 melanoma cells leila chekir-ghedira month download article/chapter article mokdad-bzeouich exert multi-target functions plant-derived coumarin derivatives facultĂ© de pharmacie full article pdf human glioblastoma cells ïżœministĂšre tunisien de privacy choices/manage cookies related subjects brain tumor epidemiology inhibited cell adhesion cancer-related death chekir-ghedira cancer cell adhesion oligomer fractions inhibited de almeida ld universitĂ© de lorraine universitĂ© de monastir u87 glioblastoma cells regulate cell proliferation collagen type iv differentiated glioblastoma cells dose dependent manner serine protease inhibitor trends cell biol mol cell biol ingĂ©nierie des biomolĂ©cules kamel ghedira anti-angiogenesis activity biochim biophys acta exp ther med laryngeal cancer cells pancreatic cancer cells tumor inhibitory activity exp ther oncol curr oncol rep european economic area synthetic substances respective receptors α2ÎČ1 promotes immune responses lipid lowering agents dopamine-induced cytotoxicityin acute gastric lesions hymenodictyon excelsum phytochemical garcĂ­a-mondragĂłn mj flavonoid-structured molecules single domain antibody

Schema {đŸ—ș}

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         headline:Esculin and its oligomer fractions inhibit adhesion and migration of U87 glioblastoma cells and in vitro angiogenesis
         description:Cancer metastasis is the major cause of cancer-related death. Chemoprevention is defined as the use of natural or synthetic substances to prevent cancer formation or cancer progress. In the present study, we investigate the antitumor activity of esculin and its oligomer fractions in U87 glioblastoma cells. We showed that esculin and its oligomers reduced U87 cell growth in a dose dependent manner. They also inhibited cell adhesion to collagen IV and vitronectin by interfering with the function of their respective receptors α2ÎČ1 and αvÎČ5 integrins. Furthermore, the tested samples were able to reduce migration of U87 cells towards another extracellular matrix fibronectin. Moreover, esculin and its oligomer fractions inhibited in vitro angiogenesis of endothelial cells (HMEC-1). In summary, our data provide the first evidence that esculin and its oligomer fractions are able to reduce adhesion, migration of glioblastoma cells and in vitro angiogenesis. Esculin and its oligomers may thus exert multi-target functions against cancer cells.
         datePublished:2015-10-12T00:00:00Z
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      headline:Esculin and its oligomer fractions inhibit adhesion and migration of U87 glioblastoma cells and in vitro angiogenesis
      description:Cancer metastasis is the major cause of cancer-related death. Chemoprevention is defined as the use of natural or synthetic substances to prevent cancer formation or cancer progress. In the present study, we investigate the antitumor activity of esculin and its oligomer fractions in U87 glioblastoma cells. We showed that esculin and its oligomers reduced U87 cell growth in a dose dependent manner. They also inhibited cell adhesion to collagen IV and vitronectin by interfering with the function of their respective receptors α2ÎČ1 and αvÎČ5 integrins. Furthermore, the tested samples were able to reduce migration of U87 cells towards another extracellular matrix fibronectin. Moreover, esculin and its oligomer fractions inhibited in vitro angiogenesis of endothelial cells (HMEC-1). In summary, our data provide the first evidence that esculin and its oligomer fractions are able to reduce adhesion, migration of glioblastoma cells and in vitro angiogenesis. Esculin and its oligomers may thus exert multi-target functions against cancer cells.
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         Esculin
         Oligomer fractions
         Glioblastoma
         Migration
         Angiogenesis
         Cancer Research
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                  address:
                     name:Laboratoire de biologie cellulaire et molĂ©culaire. FacultĂ© de MĂ©decine dentaire. UniversitĂ© de Monastir, Monastir, Tunisia
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                     name:INSERM UMR 911-CRO2, FacultĂ© de Pharmacie, Aix-Marseille UniversitĂ©, Marseille, France
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                  name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir
                  address:
                     name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir, Monastir, Tunisia
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                     name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine, Vandoeuvre-lĂšs-Nancy, France
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                     name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine, Vandoeuvre-lĂšs-Nancy, France
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                  address:
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            name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine
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               name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine, Vandoeuvre-lĂšs-Nancy, France
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               name:Laboratoire de biologie cellulaire et molĂ©culaire. FacultĂ© de MĂ©decine dentaire. UniversitĂ© de Monastir, Monastir, Tunisia
               type:PostalAddress
            type:Organization
            name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir
            address:
               name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir, Monastir, Tunisia
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:JosĂ© Luis
      affiliation:
            name:INSERM UMR 911-CRO2, FacultĂ© de Pharmacie, Aix-Marseille UniversitĂ©
            address:
               name:INSERM UMR 911-CRO2, FacultĂ© de Pharmacie, Aix-Marseille UniversitĂ©, Marseille, France
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Laboratoire de biologie cellulaire et molĂ©culaire. FacultĂ© de MĂ©decine dentaire. UniversitĂ© de Monastir, Monastir, Tunisia
      name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir, Monastir, Tunisia
      name:INSERM UMR 911-CRO2, FacultĂ© de Pharmacie, Aix-Marseille UniversitĂ©, Marseille, France
      name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir, Monastir, Tunisia
      name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine, Vandoeuvre-lĂšs-Nancy, France
      name:Laboratoire d’IngĂ©nierie des BiomolĂ©cules, ENSAIA-INPL, UniversitĂ© de Lorraine, Vandoeuvre-lĂšs-Nancy, France
      name:Laboratoire de biologie cellulaire et molĂ©culaire. FacultĂ© de MĂ©decine dentaire. UniversitĂ© de Monastir, Monastir, Tunisia
      name:UnitĂ© de Substances Naturelles Bioactives et Biotechnologie UR12ES12, FacultĂ© de Pharmacie de Monastir, UniversitĂ© de Monastir, Monastir, Tunisia
      name:INSERM UMR 911-CRO2, FacultĂ© de Pharmacie, Aix-Marseille UniversitĂ©, Marseille, France
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