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We are analyzing https://link.springer.com/article/10.1007/bf00665960.

Title:
Vascular permeability factor (VPF, VEGF) in tumor biology | Cancer and Metastasis Reviews
Description:
Vascular permeability factor (VPF), also known as vascular endothelial growth factor (VEGF), is a multifunctional cytokine expressed and secreted at high levels by many tumor cells of animal and human origin. As secreted by tumor cells, VPF/VEGF is a 34–42 kDa heparin-binding, dimeric, disulfide-bonded glycoprotein that acts directly on endothelial cells (EC) by way of specific receptors to activate phospholipase C and induce [Ca2+]i transients. Two high affinity VPF/VEGF receptors, both tyrosine kinases, have thus far been described. VPF/VEGF is likely to have a number of important roles in tumor biology related, but not limited to, the process of tumor angiogenesis. As a potent permeability factor, VPF/VEGF promotes extravasation of plasma fibrinogen, leading to fibrin deposition which alters the tumor extracellular matrix. This matrix promotes the ingrowth of macrophages, fibroblasts, and endothelial cells. Moreover, VPF/VEGF is a selective endothelial cell (EC) growth factorin vitro, and it presumably stimulates EC proliferationin vivo. Furthermore, VPF/VEGF has been found in animal and human tumor effusions by immunoassay and by functional assays and very likely accounts for the induction of malignant ascites. In addition to its role in tumors, VPF/VEGF has recently been found to have a role in wound healing and its expression by activated macrophages suggests that it probably also participates in certain types of chronic inflammation. VPF/VEGF is expressed in normal development and in certain normal adult organs, notably kidney, heart, adrenal gland and lung. Its functions in normal adult tissues are under investigation.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Science
  • Business & Finance

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“ˆ}

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🌠 Phenomenal Traffic: 5M - 10M visitors per month


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How Does Link.springer.com Make Money? {πŸ’Έ}

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Keywords {πŸ”}

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Topics {βœ’οΈ}

platelet-derived growth factor month download article/chapter growth factors time-resolved immunofluorometric assay mediate hypoxia-initiated angiogenesis vascular permeability factor vascular endothelial cells induces endothelial cell microvascular endothelial cells tumor-secreted products potent permeability factor human endothelial cells secreted angiogenic mitogen privacy choices/manage cookies growth advantagein vivo selective endothelial cell fiddes jc vpf/vegf promotes extravasation putative angiogenic factor clotting factor xiii endothelial cell biology hypoxia stimulates expression endothelial cell differentiation kdr tyrosine kinase tumor-derived polypeptide full article pdf growth factorin vitro tumor cells secrete disulfide-bonded glycoprotein van de water high affinity receptor gels induce angiogenesis induces plasminogen activators permeability-enhancing activity microvascular endothelium revisited rat corpus luteum metastasis reviews aims human gliomasin vivo cell-mediated immunity tumor cell generation tumor extracellular matrix transplantable rat sarcoma line tumor regression european economic area alternative exon splicing macromolecular tracer transport serotonin-injected mice beth israel hospital harvard medical school tumor biology related

Questions {❓}

  • Bissell MJ, Hall HG, Parry G: How does the extracellular matrix direct gene expression?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Vascular permeability factor (VPF, VEGF) in tumor biology
         description:Vascular permeability factor (VPF), also known as vascular endothelial growth factor (VEGF), is a multifunctional cytokine expressed and secreted at high levels by many tumor cells of animal and human origin. As secreted by tumor cells, VPF/VEGF is a 34–42 kDa heparin-binding, dimeric, disulfide-bonded glycoprotein that acts directly on endothelial cells (EC) by way of specific receptors to activate phospholipase C and induce [Ca2+]i transients. Two high affinity VPF/VEGF receptors, both tyrosine kinases, have thus far been described. VPF/VEGF is likely to have a number of important roles in tumor biology related, but not limited to, the process of tumor angiogenesis. As a potent permeability factor, VPF/VEGF promotes extravasation of plasma fibrinogen, leading to fibrin deposition which alters the tumor extracellular matrix. This matrix promotes the ingrowth of macrophages, fibroblasts, and endothelial cells. Moreover, VPF/VEGF is a selective endothelial cell (EC) growth factorin vitro, and it presumably stimulates EC proliferationin vivo. Furthermore, VPF/VEGF has been found in animal and human tumor effusions by immunoassay and by functional assays and very likely accounts for the induction of malignant ascites. In addition to its role in tumors, VPF/VEGF has recently been found to have a role in wound healing and its expression by activated macrophages suggests that it probably also participates in certain types of chronic inflammation. VPF/VEGF is expressed in normal development and in certain normal adult organs, notably kidney, heart, adrenal gland and lung. Its functions in normal adult tissues are under investigation.
         datePublished:
         dateModified:
         pageStart:303
         pageEnd:324
         sameAs:https://doi.org/10.1007/BF00665960
         keywords:
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            vascular endothelial growth factor
            endothelial cells
            Cancer Research
            Oncology
            Biomedicine
            general
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      headline:Vascular permeability factor (VPF, VEGF) in tumor biology
      description:Vascular permeability factor (VPF), also known as vascular endothelial growth factor (VEGF), is a multifunctional cytokine expressed and secreted at high levels by many tumor cells of animal and human origin. As secreted by tumor cells, VPF/VEGF is a 34–42 kDa heparin-binding, dimeric, disulfide-bonded glycoprotein that acts directly on endothelial cells (EC) by way of specific receptors to activate phospholipase C and induce [Ca2+]i transients. Two high affinity VPF/VEGF receptors, both tyrosine kinases, have thus far been described. VPF/VEGF is likely to have a number of important roles in tumor biology related, but not limited to, the process of tumor angiogenesis. As a potent permeability factor, VPF/VEGF promotes extravasation of plasma fibrinogen, leading to fibrin deposition which alters the tumor extracellular matrix. This matrix promotes the ingrowth of macrophages, fibroblasts, and endothelial cells. Moreover, VPF/VEGF is a selective endothelial cell (EC) growth factorin vitro, and it presumably stimulates EC proliferationin vivo. Furthermore, VPF/VEGF has been found in animal and human tumor effusions by immunoassay and by functional assays and very likely accounts for the induction of malignant ascites. In addition to its role in tumors, VPF/VEGF has recently been found to have a role in wound healing and its expression by activated macrophages suggests that it probably also participates in certain types of chronic inflammation. VPF/VEGF is expressed in normal development and in certain normal adult organs, notably kidney, heart, adrenal gland and lung. Its functions in normal adult tissues are under investigation.
      datePublished:
      dateModified:
      pageStart:303
      pageEnd:324
      sameAs:https://doi.org/10.1007/BF00665960
      keywords:
         vascular permeability factor
         vascular endothelial growth factor
         endothelial cells
         Cancer Research
         Oncology
         Biomedicine
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                     type:PostalAddress
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            name:Kiang-Teck Yeo
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               type:PostalAddress
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      name:Ann M. Dvorak
      affiliation:
            name:Beth Israel Hospital and Harvard Medical School
            address:
               name:Departments of Pathology, Beth Israel Hospital and Harvard Medical School, Boston, USA
               type:PostalAddress
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               name:Departments of Pathology, Beth Israel Hospital and Harvard Medical School, Boston, USA
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