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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/10.1186/bcr1745.

Title:
Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice | Breast Cancer Research
Description:
This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT664V-E mice). The Ingenuity knowledge database was used to characterize four functional association networks whose hub genes are directly linked to inflammation (specifically, the genes encoding IL-1β, tumour necrosis factor, interferon-γ, and monocyte chemoattractant protein-1/CC chemokine ligand-2) and are increasingly expressed during such progression. In silico meta-analysis in a human breast cancer dataset suggests that proinflammatory activation in the mammary glands of these mice reflects a general pattern of human breast cancer.
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 7,625,932 visitors per month in the current month.

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

We don't see any clear sign of profit-making.

Many websites are intended to earn money, but some serve to share ideas or build connections. Websites exist for all kinds of purposes. This might be one of them. Link.springer.com might be plotting its profit, but the way they're doing it isn't detectable yet.

Keywords {🔍}

cancer, tumour, mammary, pubmed, google, scholar, mice, genes, gene, article, cas, expression, carcinogenesis, breast, forni, progression, figure, cells, inflammation, microenvironment, neu, cell, ifnγ, data, inflammatory, transgenic, balbneutve, cavallo, gatms, ingenuity, functional, tnf, authors, database, cytokines, interleukin, musiani, analysis, association, chemokine, tumor, ilβ, human, proinflammatory, shown, growth, ccl, mcpccl, full, giovarelli,

Topics {✒️}

granulocyte-macrophage colony-stimulating factor tumour-induced angiogenic switch lymphokine-activated tumor inhibition genome-wide mouse arrays guido forni & federica cavallo lec/ccl16 rapidly neutralize marked anti-angiogenic activity dominant regulatory t-cell nf-kappab italian ministero dell'università tumor-specific immune memory powerful anti-tumour activity chemokine-based pathogenetic mechanisms tumor necrosis factor-alpha //breast-cancer-research inflammation-related gene signature inflammation-related reaction elicited gene encoding mcp-1/ccl2 mcp-1/ccl2 chemokine increases cell-mediated tumor rejection erbb signalling network ifn-gamma-producing ts/ c-erbb-2 transgenic balb/ central driving force cytokine-induced tumor immunogenicity full size image pair-wise correlation comparison metastatic murine adenocarcinoma neu-driven autochthonous carcinogenesis monocyte chemoattractant protein machine learning ifn-γ knockout mice adenocarcinoma cells engineered tsa-ifn-γ cells [10] tumor-bearing mice inhibit functional association networks long-lasting response anti-tumour vaccines privacy choices/manage cookies authors’ original file il-12 induced ifn-γ study addressed balb-neut664v human breast cancer transcription profiling search ingenuity knowledge database cc chemokine ligand breast cancer pathophysiologies mcp-1/ccl2 hub genes differentiates acute inflammation acute tumour destruction

Questions {❓}

  • Krieg AM: CpG motifs: the active ingredient in bacterial extracts?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice
         description:This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT664V-E mice). The Ingenuity knowledge database was used to characterize four functional association networks whose hub genes are directly linked to inflammation (specifically, the genes encoding IL-1β, tumour necrosis factor, interferon-γ, and monocyte chemoattractant protein-1/CC chemokine ligand-2) and are increasingly expressed during such progression. In silico meta-analysis in a human breast cancer dataset suggests that proinflammatory activation in the mammary glands of these mice reflects a general pattern of human breast cancer.
         datePublished:2007-08-10T00:00:00Z
         dateModified:2007-08-10T00:00:00Z
         pageStart:1
         pageEnd:9
         sameAs:https://doi.org/10.1186/bcr1745
         keywords:
            Mammary Gland
            Tumour Microenvironment
            Mammary Carcinogenesis
            Angiogenic Switch
            Functional Association Network
            Cancer Research
            Oncology
            Surgical Oncology
         image:
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                     address:
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      headline:Inflammation and breast cancer. Inflammatory component of mammary carcinogenesis in ErbB2 transgenic mice
      description:This review addresses genes differentially expressed in the mammary gland transcriptome during the progression of mammary carcinogenesis in BALB/c mice that are transgenic for the rat neu (ERBB2, or HER-2/neu) oncogene (BALB-neuT664V-E mice). The Ingenuity knowledge database was used to characterize four functional association networks whose hub genes are directly linked to inflammation (specifically, the genes encoding IL-1β, tumour necrosis factor, interferon-γ, and monocyte chemoattractant protein-1/CC chemokine ligand-2) and are increasingly expressed during such progression. In silico meta-analysis in a human breast cancer dataset suggests that proinflammatory activation in the mammary glands of these mice reflects a general pattern of human breast cancer.
      datePublished:2007-08-10T00:00:00Z
      dateModified:2007-08-10T00:00:00Z
      pageStart:1
      pageEnd:9
      sameAs:https://doi.org/10.1186/bcr1745
      keywords:
         Mammary Gland
         Tumour Microenvironment
         Mammary Carcinogenesis
         Angiogenic Switch
         Functional Association Network
         Cancer Research
         Oncology
         Surgical Oncology
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                  address:
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                     type:PostalAddress
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         name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
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            address:
               name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
               type:PostalAddress
            type:Organization
      name:Francesca Cordero
      affiliation:
            name:Molecular Biotechnology Center
            address:
               name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
               type:PostalAddress
            type:Organization
      name:Guido Forni
      affiliation:
            name:Molecular Biotechnology Center
            address:
               name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Federica Cavallo
      affiliation:
            name:Molecular Biotechnology Center
            address:
               name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
      name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
      name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy
      name:Department of Clinical and Biological Sciences, Molecular Biotechnology Center, Turin, Italy

External Links {🔗}(158)

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4.5s.