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  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00262-014-1606-z.

Title:
Interactions between neutrophils and non-small cell lung cancer cells: enhancement of tumor proliferation and inflammatory mediator synthesis | Cancer Immunology, Immunotherapy
Description:
The inflammatory tumor microenvironment plays a crucial role in tumor progression. In lung cancer, both bacterial infections and neutrophilia are associated with a poor prognosis. In this study, we characterized the effect of isolated human neutrophils on proliferation of the non-small cell lung cancer (NSCLC) cell line A549 and analyzed the impact of A549–neutrophil interactions on inflammatory mediator generation in naive and lipopolysaccharide (LPS)-exposed cell cultures. Co-incubation of A549 cells with neutrophils induced proliferation of resting and LPS-exposed A549 cells in a dose-dependent manner. In transwell-experiments, this effect was demonstrated to depend on direct cell-to-cell contact. This pro-proliferative effect of neutrophils on A549 cells could be attenuated by inhibition of neutrophil elastase activity, but not by oxygen radical neutralization. Correspondingly, neutrophil elastase secretion, but not respiratory burst, was specifically enhanced in co-cultures of A549 cells and neutrophils. Moreover, interference with COX-2 activity by indomethacin or the specific COX-2 inhibitor NS-398 also blunted the increased A549 proliferation in the presence of neutrophils. In parallel, a massive amplification of COX-2-dependent prostaglandin E2 synthesis was detected in A549–neutrophil co-cultures. These findings suggest that direct cell–cell interactions between neutrophils and tumor cells cause release of inflammatory mediators which, in turn, may enhance tumor growth in NSCLC.
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

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

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? {💸}

We're unsure how the site profits.

Not all websites are made for profit; some exist to inform or educate users. Or any other reason why people make websites. And this might be the case. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {🔍}

cells, neutrophils, proliferation, pubmed, cell, cancer, lung, neutrophil, google, scholar, article, elastase, cas, release, tumor, cocultures, pge, cox, mts, activity, lps, germany, experiments, performed, human, presence, absence, pmn, effect, monocultures, inflammatory, µgml, fig, role, culture, central, isolated, inhibitor, growth, medium, coculture, oxygen, mediators, activation, pmnml, incubated, nsclc, model, independent, hhbss,

Topics {✒️}

l-pyroglutamyl-l-propyl-l-valine-p-nitro-anilide chemotactic peptide n-formyl-methionyl-leucyl-phenylalanine n-formyl-methionyl-leucyl-phenylalanine fsc cd8-positive t-cell ratio phosphatidylinositol 3-kinase/akt pathway article download pdf small-cell lung cancer platelet-derived growth factor intratumoral cd66b-positive neutrophil superoxide dismutase-inhibitable reduction cox-2-derived lipid mediators neutrophil-derived inflammatory mediators key neutrophil-derived mediator cox-2-specific inhibitor ns-398 cell cycle-independent block elastase-induced cell proliferation neutrophil-induced enhanced proliferation direct cell–cell contact unspecific cox-inhibitor indomethacin direct cell–cell interactions neutrophils dose-dependently increased tumour microenvironment—dancing 2 mm l-glutamine specific cox-inhibitor indomethacin human lung carcinoma neutrophil-induced a549 proliferation actual pmn/a549 ratio neutrophile-induced a549 proliferation free arachidonic acid neutrophil elastase-mediated degradation phosphate-buffered saline neutrophil–a549 cell interactions inflammatory mediator synthesis fmlp-induced elastase secretion phenol red-free hhbss il-1 receptor antagonist full access gram-negative pulmonary infections strong pro-proliferative effect werner seeger 10 µg/ml superoxide dismutase privacy choices/manage cookies direct pro-proliferative effect dose-dependent manner inflammatory mediator generation inducing cell proliferation gregory ad integrin-linked kinase neutrophil inhibitory factor lung cancer patients

Questions {❓}

  • Balkwill F, Mantovani A (2001) Inflammation and cancer: back to Virchow?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Interactions between neutrophils and non-small cell lung cancer cells: enhancement of tumor proliferation and inflammatory mediator synthesis
         description:The inflammatory tumor microenvironment plays a crucial role in tumor progression. In lung cancer, both bacterial infections and neutrophilia are associated with a poor prognosis. In this study, we characterized the effect of isolated human neutrophils on proliferation of the non-small cell lung cancer (NSCLC) cell line A549 and analyzed the impact of A549–neutrophil interactions on inflammatory mediator generation in naive and lipopolysaccharide (LPS)-exposed cell cultures. Co-incubation of A549 cells with neutrophils induced proliferation of resting and LPS-exposed A549 cells in a dose-dependent manner. In transwell-experiments, this effect was demonstrated to depend on direct cell-to-cell contact. This pro-proliferative effect of neutrophils on A549 cells could be attenuated by inhibition of neutrophil elastase activity, but not by oxygen radical neutralization. Correspondingly, neutrophil elastase secretion, but not respiratory burst, was specifically enhanced in co-cultures of A549 cells and neutrophils. Moreover, interference with COX-2 activity by indomethacin or the specific COX-2 inhibitor NS-398 also blunted the increased A549 proliferation in the presence of neutrophils. In parallel, a massive amplification of COX-2-dependent prostaglandin E2 synthesis was detected in A549–neutrophil co-cultures. These findings suggest that direct cell–cell interactions between neutrophils and tumor cells cause release of inflammatory mediators which, in turn, may enhance tumor growth in NSCLC.
         datePublished:2014-09-04T00:00:00Z
         dateModified:2014-09-04T00:00:00Z
         pageStart:1297
         pageEnd:1306
         sameAs:https://doi.org/10.1007/s00262-014-1606-z
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            Neutrophils
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            Inflammation
            Elastase
            COX-2
            Oncology
            Immunology
            Cancer Research
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      headline:Interactions between neutrophils and non-small cell lung cancer cells: enhancement of tumor proliferation and inflammatory mediator synthesis
      description:The inflammatory tumor microenvironment plays a crucial role in tumor progression. In lung cancer, both bacterial infections and neutrophilia are associated with a poor prognosis. In this study, we characterized the effect of isolated human neutrophils on proliferation of the non-small cell lung cancer (NSCLC) cell line A549 and analyzed the impact of A549–neutrophil interactions on inflammatory mediator generation in naive and lipopolysaccharide (LPS)-exposed cell cultures. Co-incubation of A549 cells with neutrophils induced proliferation of resting and LPS-exposed A549 cells in a dose-dependent manner. In transwell-experiments, this effect was demonstrated to depend on direct cell-to-cell contact. This pro-proliferative effect of neutrophils on A549 cells could be attenuated by inhibition of neutrophil elastase activity, but not by oxygen radical neutralization. Correspondingly, neutrophil elastase secretion, but not respiratory burst, was specifically enhanced in co-cultures of A549 cells and neutrophils. Moreover, interference with COX-2 activity by indomethacin or the specific COX-2 inhibitor NS-398 also blunted the increased A549 proliferation in the presence of neutrophils. In parallel, a massive amplification of COX-2-dependent prostaglandin E2 synthesis was detected in A549–neutrophil co-cultures. These findings suggest that direct cell–cell interactions between neutrophils and tumor cells cause release of inflammatory mediators which, in turn, may enhance tumor growth in NSCLC.
      datePublished:2014-09-04T00:00:00Z
      dateModified:2014-09-04T00:00:00Z
      pageStart:1297
      pageEnd:1306
      sameAs:https://doi.org/10.1007/s00262-014-1606-z
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         Lung cancer
         Neutrophils
         A549 cells
         Inflammation
         Elastase
         COX-2
         Oncology
         Immunology
         Cancer Research
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            name:Katja Hattar
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                  address:
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            name:Katharina Franz
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                  address:
                     name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
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            name:Michael Ludwig
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                  address:
                     name:Department of Anaesthesiology, University of Giessen, Giessen, Germany
                     type:PostalAddress
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            name:Ulf Sibelius
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                  name:University of Giessen and Marburg Lung Center (UGMLC)
                  address:
                     name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
                     type:PostalAddress
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            name:Jochen Wilhelm
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                  address:
                     name:Department of Internal Medicine II, Biostatistics Group, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
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                  address:
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            name:Florentine S. B. Subtil
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                     name:Department of Radiotherapy and Radiooncology, Philipps-University, Marburg, Germany
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            name:Friedrich Grimminger
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                  address:
                     name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
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               name:Department of Anaesthesiology, University of Giessen, Giessen, Germany
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            name:University of Giessen and Marburg Lung Center (UGMLC)
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               name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
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      name:Jochen Wilhelm
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            name:University of Giessen and Marburg Lung Center (UGMLC)
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            name:University of Giessen and Marburg Lung Center (UGMLC)
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               name:Department of Internal Medicine II, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
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      name:Rajkumar Savai
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      name:Florentine S. B. Subtil
      affiliation:
            name:Philipps-University
            address:
               name:Department of Radiotherapy and Radiooncology, Philipps-University, Marburg, Germany
               type:PostalAddress
            type:Organization
      name:Gabriele Dahlem
      affiliation:
            name:University of Giessen and Marburg Lung Center (UGMLC)
            address:
               name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
               type:PostalAddress
            type:Organization
      name:Bastian Eul
      affiliation:
            name:University of Giessen and Marburg Lung Center (UGMLC)
            address:
               name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
               type:PostalAddress
            type:Organization
      name:Werner Seeger
      affiliation:
            name:Max-Planck Institute for Heart and Lung Research
            address:
               name:Max-Planck Institute for Heart and Lung Research, Bad Nauheim, Germany
               type:PostalAddress
            type:Organization
            name:University of Giessen and Marburg Lung Center (UGMLC)
            address:
               name:Department of Internal Medicine II, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
               type:PostalAddress
            type:Organization
      name:Friedrich Grimminger
      affiliation:
            name:University of Giessen and Marburg Lung Center (UGMLC)
            address:
               name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
               type:PostalAddress
            type:Organization
      name:Ulrich Grandel
      affiliation:
            name:University of Giessen and Marburg Lung Center (UGMLC)
            address:
               name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Anaesthesiology, University of Giessen, Giessen, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine II, Biostatistics Group, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine II, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Max-Planck Institute for Heart and Lung Research, Bad Nauheim, Germany
      name:Department of Radiotherapy and Radiooncology, Philipps-University, Marburg, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Max-Planck Institute for Heart and Lung Research, Bad Nauheim, Germany
      name:Department of Internal Medicine II, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany
      name:Department of Internal Medicine IV/V, University of Giessen and Marburg Lung Center (UGMLC), Giessen, Germany

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