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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
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We are analyzing https://link.springer.com/article/10.1007/s00262-013-1447-1.

Title:
Increase in CD14+HLA-DR−/low myeloid-derived suppressor cells in hepatocellular carcinoma patients and its impact on prognosis | Cancer Immunology, Immunotherapy
Description:
Myeloid-derived suppressor cells (MDSCs) are known as key immune regulators in various human malignancies, and it is reported that CD14+HLA-DR−/low MDSCs are increased in hepatocellular carcinoma (HCC) patients. However, the host factors that regulate the frequency and the effect on the prognosis of HCC patients are still unclear. We investigated these issues and clarified the relationships between a feature of MDSCs and host factors in HCC patients. We examined the frequency of MDSCs in 123 HCC patients, 30 chronic liver disease patients without HCC, and 13 healthy controls by flow cytometric analysis. The relationships between the clinical features and the frequency of MDSCs were analyzed. In 33 patients who received curative radiofrequency ablation (RFA) therapy, we examined the impact of MDSCs on HCC recurrence. The frequency of MDSCs in HCC patients was significantly increased. It was correlated with tumor progression, but not with the degree of liver fibrosis and inflammation. In terms of serum cytokines, the concentrations of IL-10, IL-13, and vascular endothelial growth factor were significantly correlated with the frequency of MDSCs. In HCC patients who received curative RFA therapy, the frequency of MDSCs after treatment showed various changes and was inversely correlated with recurrence-free survival time. The frequency of MDSCs is correlated with tumor progression, and this frequency after RFA is inversely correlated with the prognosis of HCC patients. Patients with a high frequency of MDSCs after RFA should be closely followed and the inhibition of MDSCs may improve the prognosis of patients.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Health & Fitness
  • Education

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're unsure how the site profits.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com could be getting rich in stealth mode, or the way it's monetizing isn't detectable.

Keywords {🔍}

article, pubmed, google, scholar, cells, cancer, cas, patients, carcinoma, hepatocellular, suppressor, myeloidderived, immunol, mdscs, hcc, tumor, frequency, cell, liver, factor, res, increased, radiofrequency, ablation, immune, factors, clinical, access, gastroenterology, privacy, cookies, content, cdhladrlow, prognosis, mizukoshi, rfa, correlated, growth, peripheral, myeloid, regulatory, clin, dendritic, publish, research, search, arihara, arai, yamashita, human,

Topics {✒️}

cd14+hla-dr−/low mdscs immunosuppressive cd14 + hla-drlow/- monocytes antigen-specific t-cell responses myeloid-derived suppressor cells myeloid suppressor cells month download article/chapter tatsuya yamashita & shuichi kaneko cd8 t-cell impairment related subjects recurrence-free survival time intermediate/advanced hepatocellular carcinoma article cancer immunology monocyte-derived macrophages hla-dr phase ii study cell expressed tumor-derived cytokines myeloid cells full article pdf cells hla radiofrequency thermal ablation percutaneous radiofrequency ablation privacy choices/manage cookies advanced hepatocellular carcinoma dendritic cells pulsed independent prognostic factor th2 cytokine interleukin-13 hepatocellular carcinoma patients defective antitumor function check access instant access hepatic arterial infusion metastatic tumor burden tumor-bearing mice cells correlate clinical cancer stage dendritic cell differentiation article arihara european economic area human malignancies de oliveira ac doxorubicin-cyclophosphamide chemotherapy facilitate tumor progression tumor microenvironment delays limits tumor progression conditions privacy policy radiofrequency ablation article log flow cytometric analysis electronic supplementary material

Questions {❓}

  • Lencioni R, Chen XP, Dagher L, Venook AP (2010) Treatment of intermediate/advanced hepatocellular carcinoma in the clinic: how can outcomes be improved?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Increase in CD14+HLA-DR−/low myeloid-derived suppressor cells in hepatocellular carcinoma patients and its impact on prognosis
         description:Myeloid-derived suppressor cells (MDSCs) are known as key immune regulators in various human malignancies, and it is reported that CD14+HLA-DR−/low MDSCs are increased in hepatocellular carcinoma (HCC) patients. However, the host factors that regulate the frequency and the effect on the prognosis of HCC patients are still unclear. We investigated these issues and clarified the relationships between a feature of MDSCs and host factors in HCC patients. We examined the frequency of MDSCs in 123 HCC patients, 30 chronic liver disease patients without HCC, and 13 healthy controls by flow cytometric analysis. The relationships between the clinical features and the frequency of MDSCs were analyzed. In 33 patients who received curative radiofrequency ablation (RFA) therapy, we examined the impact of MDSCs on HCC recurrence. The frequency of MDSCs in HCC patients was significantly increased. It was correlated with tumor progression, but not with the degree of liver fibrosis and inflammation. In terms of serum cytokines, the concentrations of IL-10, IL-13, and vascular endothelial growth factor were significantly correlated with the frequency of MDSCs. In HCC patients who received curative RFA therapy, the frequency of MDSCs after treatment showed various changes and was inversely correlated with recurrence-free survival time. The frequency of MDSCs is correlated with tumor progression, and this frequency after RFA is inversely correlated with the prognosis of HCC patients. Patients with a high frequency of MDSCs after RFA should be closely followed and the inhibition of MDSCs may improve the prognosis of patients.
         datePublished:2013-06-14T00:00:00Z
         dateModified:2013-06-14T00:00:00Z
         pageStart:1421
         pageEnd:1430
         sameAs:https://doi.org/10.1007/s00262-013-1447-1
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            Hepatocellular carcinoma
            Radiofrequency ablation
            Recurrence
            Cancer
            Oncology
            Immunology
            Cancer Research
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                        type:PostalAddress
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ScholarlyArticle:
      headline:Increase in CD14+HLA-DR−/low myeloid-derived suppressor cells in hepatocellular carcinoma patients and its impact on prognosis
      description:Myeloid-derived suppressor cells (MDSCs) are known as key immune regulators in various human malignancies, and it is reported that CD14+HLA-DR−/low MDSCs are increased in hepatocellular carcinoma (HCC) patients. However, the host factors that regulate the frequency and the effect on the prognosis of HCC patients are still unclear. We investigated these issues and clarified the relationships between a feature of MDSCs and host factors in HCC patients. We examined the frequency of MDSCs in 123 HCC patients, 30 chronic liver disease patients without HCC, and 13 healthy controls by flow cytometric analysis. The relationships between the clinical features and the frequency of MDSCs were analyzed. In 33 patients who received curative radiofrequency ablation (RFA) therapy, we examined the impact of MDSCs on HCC recurrence. The frequency of MDSCs in HCC patients was significantly increased. It was correlated with tumor progression, but not with the degree of liver fibrosis and inflammation. In terms of serum cytokines, the concentrations of IL-10, IL-13, and vascular endothelial growth factor were significantly correlated with the frequency of MDSCs. In HCC patients who received curative RFA therapy, the frequency of MDSCs after treatment showed various changes and was inversely correlated with recurrence-free survival time. The frequency of MDSCs is correlated with tumor progression, and this frequency after RFA is inversely correlated with the prognosis of HCC patients. Patients with a high frequency of MDSCs after RFA should be closely followed and the inhibition of MDSCs may improve the prognosis of patients.
      datePublished:2013-06-14T00:00:00Z
      dateModified:2013-06-14T00:00:00Z
      pageStart:1421
      pageEnd:1430
      sameAs:https://doi.org/10.1007/s00262-013-1447-1
      keywords:
         Myeloid-derived suppressor cells
         Hepatocellular carcinoma
         Radiofrequency ablation
         Recurrence
         Cancer
         Oncology
         Immunology
         Cancer Research
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            1432-0851
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            name:Fumitaka Arihara
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                     name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
                     type:PostalAddress
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            name:Eishiro Mizukoshi
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                     type:PostalAddress
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            name:Masaaki Kitahara
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                     type:PostalAddress
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                  address:
                     name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
                     type:PostalAddress
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                  name:University of Fukui
                  address:
                     name:Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka, Japan
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Shuichi Kaneko
            affiliation:
                  name:Kanazawa University
                  address:
                     name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
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         name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
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      address:
         name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
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         name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
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         name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
         type:PostalAddress
      name:Kanazawa University
      address:
         name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
         type:PostalAddress
      name:University of Fukui
      address:
         name:Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka, Japan
         type:PostalAddress
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      address:
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         type:PostalAddress
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      name:Fumitaka Arihara
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      email:[email protected]
      name:Eishiro Mizukoshi
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      name:Masaaki Kitahara
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      name:Yoshiko Takata
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      name:Kuniaki Arai
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      name:Tatsuya Yamashita
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
      name:Yasunari Nakamoto
      affiliation:
            name:University of Fukui
            address:
               name:Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka, Japan
               type:PostalAddress
            type:Organization
      name:Shuichi Kaneko
      affiliation:
            name:Kanazawa University
            address:
               name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
      name:Second Department of Internal Medicine, Faculty of Medical Sciences, University of Fukui, Matsuoka, Japan
      name:Department of Gastroenterology, Graduate School of Medicine, Kanazawa University, Kanazawa, Japan
WebPageElement:
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External Links {🔗}(160)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

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