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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s10555-011-9310-3.

Title:
Cyclooxygenases and lipoxygenases in cancer | Cancer and Metastasis Reviews
Description:
Cancer initiation and progression are multistep events that require cell proliferation, migration, extravasation to the blood or lymphatic vessels, arrest to the metastatic site, and ultimately secondary growth. Tumor cell functions at both primary or secondary sites are controlled by many different factors, including growth factors and their receptors, chemokines, nuclear receptors, cell–cell interactions, cell–matrix interactions, as well as oxygenated metabolites of arachidonic acid. The observation that cyclooxygenases and lipoxygenases and their arachidonic acid-derived eicosanoid products (prostanoids and HETEs) are expressed and produced by tumor cells, together with the finding that these enzymes can regulate cell growth, survival, migration, and invasion, has prompted investigators to analyze the roles of these enzymes in cancer progression. In this review, we focus on the contribution of cyclooxygenase- and lipoxygenase-derived eicosanoids to tumor cell function in vitro and in vivo and discuss hope and tribulations of targeting these enzymes for cancer prevention and treatment.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

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.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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How Does Link.springer.com Make Money? {💸}

We find it hard to spot revenue streams.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

google, scholar, pubmed, cas, cancer, lipoxygenase, receptor, cell, journal, cells, research, prostaglandin, growth, human, tumor, cyclooxygenase, lung, expression, cox, inhibition, acid, chemistry, biological, angiogenesis, carcinogenesis, chen, inhibitors, role, thromboxane, endothelial, pharmacology, prostate, lox, colon, synthase, signaling, metastasis, factor, molecular, apoptosis, effects, article, pozzi, yang, pathway, experimental, biochemical, tang, mouse, oncogene,

Topics {✒️}

peroxisome proliferator-activated receptor-γ n-aroyl-tetrahydro-gamma-carbolines acylnitroso hetero-diels-alder cycloadducts pgf2alpha-f-prostanoid receptor signalling ep4-betaarrestin1-c-src signalsome f-prostanoid receptor signalling extracellular signal-regulated kinases f-series-prostanoid receptor prostaglandin e-type receptor f-prostanoid receptor regulation linoleic acid-dependent growth pi3k-akt signalling pathways small-cell lung cancer month download article/chapter calcium-calcineurin-nfat pathway phospatidylinositol-3-kinase/akt ppar diminished lipocalin-type prostaglandin nuclear factor-kappab activation aspirin-triggered lipoxin a4 nonsteroidal anti-inflammatory drugs uv-induced skin carcinogenesis castration-resistant prostate cancer anti-inflammatory cyclopentenone prostaglandins vascular integrin alpha prostaglandin e2 results thromboxane synthase signaling c17-hydroxy acids catalyzed promotes cell proliferation ep4 receptor antagonist promotes adipocyte differentiation suppresses colon carcinogenesis prostaglandin-independent pathway structure-activity relationship studies ppar-gamma activity prostaglandin d2 receptor pge2 receptor ep2 anti-tumorigenic effects microvascular endothelial cells focal adhesion assembly lipocalin-type prostaglandin 5-lipoxygenase pathway suppresses including growth factors privacy choices/manage cookies receptor subtype ep3 regulates ppar-delta frizzled 9-dependent pathway endothelial cell function lung cancer cells colon cancer cells cell–cell interactions

Questions {❓}

  • A new avenue in anti-inflammatory therapy?
  • Nonsteroidal anti-inflammatory drugs and the heart: what is the danger?

Schema {🗺️}

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         headline:Cyclooxygenases and lipoxygenases in cancer
         description:Cancer initiation and progression are multistep events that require cell proliferation, migration, extravasation to the blood or lymphatic vessels, arrest to the metastatic site, and ultimately secondary growth. Tumor cell functions at both primary or secondary sites are controlled by many different factors, including growth factors and their receptors, chemokines, nuclear receptors, cell–cell interactions, cell–matrix interactions, as well as oxygenated metabolites of arachidonic acid. The observation that cyclooxygenases and lipoxygenases and their arachidonic acid-derived eicosanoid products (prostanoids and HETEs) are expressed and produced by tumor cells, together with the finding that these enzymes can regulate cell growth, survival, migration, and invasion, has prompted investigators to analyze the roles of these enzymes in cancer progression. In this review, we focus on the contribution of cyclooxygenase- and lipoxygenase-derived eicosanoids to tumor cell function in vitro and in vivo and discuss hope and tribulations of targeting these enzymes for cancer prevention and treatment.
         datePublished:2011-10-15T00:00:00Z
         dateModified:2011-10-15T00:00:00Z
         pageStart:277
         pageEnd:294
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            Thromboxane
            Prostacyclin
            Prostaglandins
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            Oncology
            Biomedicine
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      headline:Cyclooxygenases and lipoxygenases in cancer
      description:Cancer initiation and progression are multistep events that require cell proliferation, migration, extravasation to the blood or lymphatic vessels, arrest to the metastatic site, and ultimately secondary growth. Tumor cell functions at both primary or secondary sites are controlled by many different factors, including growth factors and their receptors, chemokines, nuclear receptors, cell–cell interactions, cell–matrix interactions, as well as oxygenated metabolites of arachidonic acid. The observation that cyclooxygenases and lipoxygenases and their arachidonic acid-derived eicosanoid products (prostanoids and HETEs) are expressed and produced by tumor cells, together with the finding that these enzymes can regulate cell growth, survival, migration, and invasion, has prompted investigators to analyze the roles of these enzymes in cancer progression. In this review, we focus on the contribution of cyclooxygenase- and lipoxygenase-derived eicosanoids to tumor cell function in vitro and in vivo and discuss hope and tribulations of targeting these enzymes for cancer prevention and treatment.
      datePublished:2011-10-15T00:00:00Z
      dateModified:2011-10-15T00:00:00Z
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         Cancer
         Eicosanoids
         Thromboxane
         Prostacyclin
         Prostaglandins
         Inhibitors
         Cancer Research
         Oncology
         Biomedicine
         general
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      address:
         name:Department of Medicine, Vanderbilt University Medical School, Nashville, USA
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               name:Department of Pharmacology, Vanderbilt University Medical School, Nashville, USA
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            address:
               name:Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical School, Nashville, USA
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      name:Ambra Pozzi
      affiliation:
            name:Vanderbilt University Medical School
            address:
               name:Department of Medicine, Vanderbilt University Medical School, Nashville, USA
               type:PostalAddress
            type:Organization
            name:Vanderbilt University Medical School
            address:
               name:Department of Cancer Biology, Vanderbilt University Medical School, Nashville, USA
               type:PostalAddress
            type:Organization
            name:Veterans Affairs Hospitals
            address:
               name:Veterans Affairs Hospitals, Nashville, USA
               type:PostalAddress
            type:Organization
            name:Vanderbilt University
            address:
               name:Departments of Medicine and Cancer Biology, Division of Nephrology and Hypertension, Vanderbilt University, Nashville, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
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      name:Vanderbilt Institute of Chemical Biology, Vanderbilt University Medical School, Nashville, USA
      name:Department of Medicine, Vanderbilt University Medical School, Nashville, USA
      name:Department of Cancer Biology, Vanderbilt University Medical School, Nashville, USA
      name:Veterans Affairs Hospitals, Nashville, USA
      name:Departments of Medicine and Cancer Biology, Division of Nephrology and Hypertension, Vanderbilt University, Nashville, USA
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External Links {🔗}(390)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
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CDN Services {📦}

  • Crossref

6.32s.