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  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
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We are analyzing https://link.springer.com/article/10.1007/s10585-008-9170-6.

Title:
Epithelial mesenchymal transition traits in human breast cancer cell lines | Clinical & Experimental Metastasis
Description:
Epithelial mesenchymal transition (EMT) has long been associated with breast cancer cell invasiveness and evidence of EMT processes in clinical samples is growing rapidly. Genome-wide transcriptional profiling of increasingly larger numbers of human breast cancer (HBC) cell lines have confirmed the existence of a subgroup of cell lines (termed Basal B/Mesenchymal) with enhanced invasive properties and a predominantly mesenchymal gene expression signature, distinct from subgroups with predominantly luminal (termed Luminal) or mixed basal/luminal (termed Basal A) features (Neve et al Cancer Cell 2006). Studies providing molecular and cellular analyses of EMT features in these cell lines are summarised, and the expression levels of EMT-associated factors in these cell lines are analysed. Recent clinical studies supporting the presence of EMT-like changes in vivo are summarised. Human breast cancer cell lines with mesenchymal properties continue to hold out the promise of directing us towards key mechanisms at play in the metastatic dissemination of breast cancer.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Education
  • Health & Fitness
  • Telecommunications

Content Management System {šŸ“}

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 {šŸ“ˆ}

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 7,603,974 visitors per month in the current month.

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How Does Link.springer.com Make Money? {šŸ’ø}

We're unsure if the website is profiting.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com could have a money-making trick up its sleeve, but it's undetectable for now.

Keywords {šŸ”}

google, scholar, pubmed, article, cas, cancer, breast, cell, transition, cells, epithelial, human, res, carcinoma, expression, mesenchymal, thompson, lines, epithelialmesenchymal, metastasis, biol, gene, mammary, growth, progression, snail, research, factor, mol, transitions, newgreen, ecadherin, clin, metastatic, stem, receptor, tumor, epithelialtomesenchymal, oncogene, invasion, vimentin, waltham, emt, access, ackland, slug, twist, protein, privacy, cookies,

Topics {āœ’ļø}

upregulated mt1-mmp/timp-2 axis tsu-pr1-b1/b2 model month download article/chapter human breast cancer-observations e-cadherin transcriptional downregulation zinc-finger protein helix-loop-helix motif k-atpase beta1-subunit genome-wide transcriptional profiling e-cadherin preserved tumors confers epithelial-mesenchymal transition stem cell characteristics contract de-ac03-76sf00098 prostate cell lines n-cadherin promotes motility epithelial-mesenchymal cell transformation growth factor receptor mammary epithelial cells human breast cancer mesenchymal transition mediated mixed basal/luminal breast cancer cells full article pdf differentiated human breast oncoprotein beta-catenin human breast tumours homotypic cell adhesion nuclear factor-{kappa} mammary gland regeneration pancreatic cancer cells human aromatase gene constitutively active type invasive breast cancer privacy choices/manage cookies e-cadherin expression selectively inhibits growth tumor cell plasticity m14 melanoma cells epithelial-mesenchymal transition epithelial mesenchymal transition human cancer progression hepatocellular carcinoma metastasis transcription factor zeb1 army medical research tumor suppressor gene epithelial-mesenchymal transitions epithelial mesenchymal transitions mesenchymal––epithelial transitions mesenchymal—epithelial transitions transitional cell carcinoma

Questions {ā“}

  • Korsching E, Packeisen J, Liedtke C etĀ al (2005) The origin of vimentin expression in invasive breast cancer: epithelial-mesenchymal transition, myoepithelial histogenesis or histogenesis from progenitor cells with bilinear differentiation potential?
  • Peinado H, Olmeda D, Cano A (2007) Snail, Zeb and bHLH factors in tumour progression: an alliance against the epithelial phenotype?
  • Thompson EW, Newgreen DF, Tarin D (2005) Carcinoma invasion and metastasis: a role for epithelial-mesenchymal transition?

Schema {šŸ—ŗļø}

WebPage:
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         headline:Epithelial mesenchymal transition traits in human breast cancer cell lines
         description:Epithelial mesenchymal transition (EMT) has long been associated with breast cancer cell invasiveness and evidence of EMT processes in clinical samples is growing rapidly. Genome-wide transcriptional profiling of increasingly larger numbers of human breast cancer (HBC) cell lines have confirmed the existence of a subgroup of cell lines (termed Basal B/Mesenchymal) with enhanced invasive properties and a predominantly mesenchymal gene expression signature, distinct from subgroups with predominantly luminal (termed Luminal) or mixed basal/luminal (termed Basal A) features (Neve etĀ al Cancer Cell 2006). Studies providing molecular and cellular analyses of EMT features in these cell lines are summarised, and the expression levels of EMT-associated factors in these cell lines are analysed. Recent clinical studies supporting the presence of EMT-like changes inĀ vivo are summarised. Human breast cancer cell lines with mesenchymal properties continue to hold out the promise of directing us towards key mechanisms at play in the metastatic dissemination of breast cancer.
         datePublished:2008-05-07T00:00:00Z
         dateModified:2008-05-07T00:00:00Z
         pageStart:629
         pageEnd:642
         sameAs:https://doi.org/10.1007/s10585-008-9170-6
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            Cancer Research
            Biomedicine
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            Hematology
            Surgical Oncology
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      headline:Epithelial mesenchymal transition traits in human breast cancer cell lines
      description:Epithelial mesenchymal transition (EMT) has long been associated with breast cancer cell invasiveness and evidence of EMT processes in clinical samples is growing rapidly. Genome-wide transcriptional profiling of increasingly larger numbers of human breast cancer (HBC) cell lines have confirmed the existence of a subgroup of cell lines (termed Basal B/Mesenchymal) with enhanced invasive properties and a predominantly mesenchymal gene expression signature, distinct from subgroups with predominantly luminal (termed Luminal) or mixed basal/luminal (termed Basal A) features (Neve etĀ al Cancer Cell 2006). Studies providing molecular and cellular analyses of EMT features in these cell lines are summarised, and the expression levels of EMT-associated factors in these cell lines are analysed. Recent clinical studies supporting the presence of EMT-like changes inĀ vivo are summarised. Human breast cancer cell lines with mesenchymal properties continue to hold out the promise of directing us towards key mechanisms at play in the metastatic dissemination of breast cancer.
      datePublished:2008-05-07T00:00:00Z
      dateModified:2008-05-07T00:00:00Z
      pageStart:629
      pageEnd:642
      sameAs:https://doi.org/10.1007/s10585-008-9170-6
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         EMT
         Basal
         Luminal
         Mesenchymal
         Breast cancer
         Breast cancer stem cells
         Cancer Research
         Biomedicine
         general
         Oncology
         Hematology
         Surgical Oncology
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                     name:Faculty of Medicine, Brawijaya University, East Java, Indonesia
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         name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital, Fitzroy, Australia
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      name:Brawijaya University
      address:
         name:Faculty of Medicine, Brawijaya University, East Java, Indonesia
         type:PostalAddress
      name:Murdoch Children’s Research Institute, The Royal Children’s Hospital
      address:
         name:Embryology Laboratory, Murdoch Children’s Research Institute, The Royal Children’s Hospital, Parkville, Australia
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         name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
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      address:
         name:Department of Genetics and Genomics, Boston University School of Medicine, Boston, USA
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         name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
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      name:Lawrence Berkeley National Laboratory
      address:
         name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
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            address:
               name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
               type:PostalAddress
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               name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital, Fitzroy, Australia
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               name:Embryology Laboratory, Murdoch Children’s Research Institute, The Royal Children’s Hospital, Parkville, Australia
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      name:M. Waltham
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               name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
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               name:Department of Genetics and Genomics, Boston University School of Medicine, Boston, USA
               type:PostalAddress
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            name:Lawrence Berkeley National Laboratory
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               name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
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      name:R. M. Neve
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            name:Lawrence Berkeley National Laboratory
            address:
               name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
               type:PostalAddress
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      name:E. W. Thompson
      affiliation:
            name:St. Vincent’s Institute
            address:
               name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
               type:PostalAddress
            type:Organization
            name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital
            address:
               name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital, Fitzroy, Australia
               type:PostalAddress
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      name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
      name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital, Fitzroy, Australia
      name:Faculty of Medicine, Brawijaya University, East Java, Indonesia
      name:Embryology Laboratory, Murdoch Children’s Research Institute, The Royal Children’s Hospital, Parkville, Australia
      name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
      name:Department of Genetics and Genomics, Boston University School of Medicine, Boston, USA
      name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
      name:Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, USA
      name:VBCRC Invasion and Metastasis Unit, St. Vincent’s Institute, Melbourne, Australia
      name:University of Melbourne, Department of Surgery, St. Vincent’s Hospital, Fitzroy, Australia
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External Links {šŸ”—}(297)

Analytics and Tracking {šŸ“Š}

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