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We are analyzing https://link.springer.com/article/10.1186/s12953-014-0050-5.

Title:
New insights in the composition of extracellular vesicles from pancreatic cancer cells: implications for biomarkers and functions | Proteome Science
Description:
Background Pancreatic cancer development is associated with characteristic alterations like desmoplastic reaction and immune escape which are mediated by the cell-cell communication mechanism and by the microenvironment of the cells. The whole of released components are important determinants in these processes. Especially the extracellular vesicles released by pancreatic cancer cells play a role in cell communication and modulate cell growth and immune responses. Results Here, we present the proteomic description of affinity purified extracellular vesicles from pancreatic tumour cells, compared to the secretome, defined as the whole of the proteins released by pancreatic cancer cells. The proteomic data provide comprehensive catalogues of hundreds of proteins, and the comparison reveals a special proteomic composition of pancreatic cancer cell derived extracellular vesicles. The functional analysis of the protein composition displayed that membrane proteins, glycoproteins, small GTP binding proteins and a further, heterogeneous group of proteins are enriched in vesicles, whereas proteins derived from proteasomes and ribosomes, as well as metabolic enzymes, are not components of the vesicles. Furthermore proteins playing a role in carcinogenesis and modulators of the extracellular matrix (ECM) or cell-cell interactions are components of affinity purified extracellular vesicles. Conclusion The data deepen the knowledge of extracellular vesicle composition by hundreds of proteins that have not been previously described as vesicle components released by pancreatic cancer cells. Extracellular vesicles derived from pancreatic cancer cells show common proteins shared with other vesicles as well as cell type specific proteins indicating biomarker candidates and suggesting functional roles in cancer cell stroma interactions.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Fitness & Wellness
  • 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 7,626,432 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.

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 {🔍}

proteins, samples, cells, affinity, evs, cancer, cell, pancreatic, pubmed, vesicles, article, protein, crude, paca, google, scholar, pure, figure, cas, panc, extracellular, membrane, purification, secretome, exosomes, file, data, enriched, found, preparations, germany, analysis, released, line, tumour, derived, additional, peptides, number, immune, specific, tacstdepcam, central, components, proteomic, mass, measured, release, sample, secretomes,

Topics {✒️}

susanne klein-scory genetic profile article klein-scory nathalie wojtalewicz d'souza-schorey author information authors regulate cxcr4-mediated signalling anti-tacstd1/epcam coated beads mahnaz moradian tehrani de/ethik/download/deklaration_helsinki_2008_engl mascot search engine sigma-alrich chemie gmbh transcriptomic profiles sigma-aldrich chemie gmbh article download pdf tissue-specific protein signature protein database search pancreatic cancer-derived exosomes proteins jup/gamma catenin species-specific secondary antibodies author correspondence sophisticated cell–cell communication open access license cancer cell-derived exosomes organ-specific metastatic potential potential cancer biomarker semi-dry blotting procedure nanoscale lc-ms analysis klein-scory small gtp-binding proteins ev-mediated carcinogenic mechanisms schwarte-waldhoff cell-cell communication mechanism exosome-mediated transfer cancer biomarker discovery promote tumour growth fluorescence-conjugated antibodies detecting restricted view nt5e/cd73 positive vesicles growth promoting state full size image depth view salivary biomarker development pancreatic cancer cell human colorectal cancer poor prognostic biomarker privacy choices/manage cookies tacstd1/epcam anchor protein mass spectrometric analyses tacstd1/epcam expressing cells

Questions {❓}

  • Are EV cancer specific proteins suitable as biomarkers and as anchors for vesicle isolation from body fluids?
  • Are epithelially derived pancreatic cancer cells the exclusive sources of the EV specific proteins found in the ascites of cancer patients?
  • Webber J, Clayton A: How pure are your vesicles?

Schema {🗺️}

WebPage:
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         description:Pancreatic cancer development is associated with characteristic alterations like desmoplastic reaction and immune escape which are mediated by the cell-cell communication mechanism and by the microenvironment of the cells. The whole of released components are important determinants in these processes. Especially the extracellular vesicles released by pancreatic cancer cells play a role in cell communication and modulate cell growth and immune responses. Here, we present the proteomic description of affinity purified extracellular vesicles from pancreatic tumour cells, compared to the secretome, defined as the whole of the proteins released by pancreatic cancer cells. The proteomic data provide comprehensive catalogues of hundreds of proteins, and the comparison reveals a special proteomic composition of pancreatic cancer cell derived extracellular vesicles. The functional analysis of the protein composition displayed that membrane proteins, glycoproteins, small GTP binding proteins and a further, heterogeneous group of proteins are enriched in vesicles, whereas proteins derived from proteasomes and ribosomes, as well as metabolic enzymes, are not components of the vesicles. Furthermore proteins playing a role in carcinogenesis and modulators of the extracellular matrix (ECM) or cell-cell interactions are components of affinity purified extracellular vesicles. The data deepen the knowledge of extracellular vesicle composition by hundreds of proteins that have not been previously described as vesicle components released by pancreatic cancer cells. Extracellular vesicles derived from pancreatic cancer cells show common proteins shared with other vesicles as well as cell type specific proteins indicating biomarker candidates and suggesting functional roles in cancer cell stroma interactions.
         datePublished:2014-11-18T00:00:00Z
         dateModified:2014-11-18T00:00:00Z
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            Exosome
            Secretome
            Proteomics
            Affinity purification
            Biomarker
            Pancreatic cancer
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      headline:New insights in the composition of extracellular vesicles from pancreatic cancer cells: implications for biomarkers and functions
      description:Pancreatic cancer development is associated with characteristic alterations like desmoplastic reaction and immune escape which are mediated by the cell-cell communication mechanism and by the microenvironment of the cells. The whole of released components are important determinants in these processes. Especially the extracellular vesicles released by pancreatic cancer cells play a role in cell communication and modulate cell growth and immune responses. Here, we present the proteomic description of affinity purified extracellular vesicles from pancreatic tumour cells, compared to the secretome, defined as the whole of the proteins released by pancreatic cancer cells. The proteomic data provide comprehensive catalogues of hundreds of proteins, and the comparison reveals a special proteomic composition of pancreatic cancer cell derived extracellular vesicles. The functional analysis of the protein composition displayed that membrane proteins, glycoproteins, small GTP binding proteins and a further, heterogeneous group of proteins are enriched in vesicles, whereas proteins derived from proteasomes and ribosomes, as well as metabolic enzymes, are not components of the vesicles. Furthermore proteins playing a role in carcinogenesis and modulators of the extracellular matrix (ECM) or cell-cell interactions are components of affinity purified extracellular vesicles. The data deepen the knowledge of extracellular vesicle composition by hundreds of proteins that have not been previously described as vesicle components released by pancreatic cancer cells. Extracellular vesicles derived from pancreatic cancer cells show common proteins shared with other vesicles as well as cell type specific proteins indicating biomarker candidates and suggesting functional roles in cancer cell stroma interactions.
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      dateModified:2014-11-18T00:00:00Z
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         Extracellular vesicles
         Exosome
         Secretome
         Proteomics
         Affinity purification
         Biomarker
         Pancreatic cancer
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            address:
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               type:PostalAddress
            type:Organization
      name:Wolff Schmiegel
      affiliation:
            name:Ruhr-University Bochum
            address:
               name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
               type:PostalAddress
            type:Organization
            name:Ruhr-University Bochum
            address:
               name:Medical Department, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
               type:PostalAddress
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      name:Irmgard Schwarte-Waldhoff
      affiliation:
            name:Ruhr-University Bochum
            address:
               name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
               type:PostalAddress
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      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:Functional Proteome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany
      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:Functional Proteome Analysis, German Cancer Research Center (DKFZ), Heidelberg, Germany
      name:Molecular Gastrointestinal Oncology MGO, Ruhr-University Bochum, Bochum, Germany
      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:Medical Department, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany
      name:IMBL, Medical Clinic Knappschaftskrankenhaus Bochum GmbH, Ruhr-University Bochum, Bochum, Germany

External Links {🔗}(227)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
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  • Crossref

5.28s.