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We began analyzing https://link.springer.com/article/10.1007/s00428-017-2103-5, but it redirected us to https://link.springer.com/article/10.1007/s00428-017-2103-5. The analysis below is for the second page.

Title[redir]:
The relationship between breast cancer molecular subtypes and mast cell populations in tumor microenvironment | Virchows Archiv
Description:
Mast cells (MCs) are a part of the innate immune system. The MC functions toward cancer are partially based on the release of chymase and tryptase. However, the MC effect on breast cancer is controversial. The aim of our study was to investigate the presence of MCs in breast cancer tumors of different molecular subtypes and their relationships with other pathological prognostic factors. Tryptase- and chymase-positive mast cell densities were evaluated by immunohistochemistry in 108 primary invasive breast cancer tissue samples. Positive cells were counted within the tumor bed and at the invasive margin. For all analyzed MC subpopulations, we observed statistically significant differences between individual molecular subtypes of breast cancer. The significantly higher numbers of intratumoral chymase- and tryptase-positive mast cells were observed in luminal A and luminal B tumors compared to triple-negative and HER2+ non-luminal lesions. A denser MC infiltration was associated with lower tumor grade, higher ER and PR expression, lower proliferation rate as well as the lack of HER2 overexpression. The results obtained in our study indicate a possible association of chymase- and tryptase-positive MCs with more favorable cancer immunophenotype and with beneficial prognostic indicators in breast cancer.

Matching Content Categories {馃摎}

  • Education
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Traffic Estimate {馃搱}

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


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Keywords {馃攳}

cancer, breast, cells, mcs, mast, google, scholar, tumor, pubmed, article, cell, tryptasepositive, tryptase, molecular, cases, intratumoral, luminal, study, expression, cancers, table, chymase, tumors, observed, invasive, cas, subtypes, density, higher, number, positive, patients, angiogenesis, authors, chymasepositive, significant, size, central, margin, significantly, infiltration, progression, compared, human, factor, content, full, prognostic, densities, tissue,

Topics {鉁掞笍}

archival hematoxylin鈥揺osin-stained slides mast-cell-specific serine proteases article download pdf scf/c-kit signaling clinical oncology/college primary mammary tumors anova kruskal鈥搘allis test high-dimensional protein multiplexing high-grade cancer suppressed minimum hormone-receptive cancers tryptase-positive cell densities triple-negative breast cancer breast cancer metastasis鈥攊nsight da silva ezm stem cell factor cancer tumor-host interface mast cell biology node-negative breast cancer tryptase-positive mast cells tryptase-positive mc densities tryptase-positive mc content intratumoral tryptase-positive cells chymase-positive mast cells chymase-positive mc densities intratumoral chymase-positive cells mast-cell chymase increase intratumoral tryptase-positive mcs tryptase-positive intratumoral mcs katarzyna ewa tyrak della rovere jagiellonian university committee chymase-positive mcs increased sentinel lymph nodes chymase-positive mcs correlated peritumoral tryptase-positive mcs increased mc migration full access intratumoral chymase-positive mcs tnbc triple-negative subtype privacy choices/manage cookies mast cell populations anova kruskal鈥搘allis early breast cancer campos mr de innate immune system breast cancer subtypes axillary lymph nodes pathological prognostic factors breast cancer quantified murine breast cancer

Questions {鉂搣

  • Dyduch G, Kaczmarczyk K, Oko艅 K (2012) Mast cells and cancer: enemies or allies?

Schema {馃椇锔弣

WebPage:
      mainEntity:
         headline:The relationship between breast cancer molecular subtypes and mast cell populations in tumor microenvironment
         description:Mast cells (MCs) are a part of the innate immune system. The MC functions toward cancer are partially based on the release of chymase and tryptase. However, the MC effect on breast cancer is controversial. The aim of our study was to investigate the presence of MCs in breast cancer tumors of different molecular subtypes and their relationships with other pathological prognostic factors. Tryptase- and chymase-positive mast cell densities were evaluated by immunohistochemistry in 108 primary invasive breast cancer tissue samples. Positive cells were counted within the tumor bed and at the invasive margin. For all analyzed MC subpopulations, we observed statistically significant differences between individual molecular subtypes of breast cancer. The significantly higher numbers of intratumoral chymase- and tryptase-positive mast cells were observed in luminal A and luminal B tumors compared to triple-negative and HER2+ non-luminal lesions. A denser MC infiltration was associated with lower tumor grade, higher ER and PR expression, lower proliferation rate as well as the lack of HER2 overexpression. The results obtained in our study indicate a possible association of chymase- and tryptase-positive MCs with more favorable cancer immunophenotype and with beneficial prognostic indicators in breast cancer.
         datePublished:2017-03-18T00:00:00Z
         dateModified:2017-03-18T00:00:00Z
         pageStart:505
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            Mast cells
            Breast cancer
            Molecular classification
            Pathology
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ScholarlyArticle:
      headline:The relationship between breast cancer molecular subtypes and mast cell populations in tumor microenvironment
      description:Mast cells (MCs) are a part of the innate immune system. The MC functions toward cancer are partially based on the release of chymase and tryptase. However, the MC effect on breast cancer is controversial. The aim of our study was to investigate the presence of MCs in breast cancer tumors of different molecular subtypes and their relationships with other pathological prognostic factors. Tryptase- and chymase-positive mast cell densities were evaluated by immunohistochemistry in 108 primary invasive breast cancer tissue samples. Positive cells were counted within the tumor bed and at the invasive margin. For all analyzed MC subpopulations, we observed statistically significant differences between individual molecular subtypes of breast cancer. The significantly higher numbers of intratumoral chymase- and tryptase-positive mast cells were observed in luminal A and luminal B tumors compared to triple-negative and HER2+ non-luminal lesions. A denser MC infiltration was associated with lower tumor grade, higher ER and PR expression, lower proliferation rate as well as the lack of HER2 overexpression. The results obtained in our study indicate a possible association of chymase- and tryptase-positive MCs with more favorable cancer immunophenotype and with beneficial prognostic indicators in breast cancer.
      datePublished:2017-03-18T00:00:00Z
      dateModified:2017-03-18T00:00:00Z
      pageStart:505
      pageEnd:515
      sameAs:https://doi.org/10.1007/s00428-017-2103-5
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         Mast cells
         Breast cancer
         Molecular classification
         Pathology
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                     type:PostalAddress
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               type:PostalAddress
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      name:Florence Chan
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            name:Jagiellonian University Medical College
            address:
               name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
               type:PostalAddress
            type:Organization
      name:Joanna Streb
      affiliation:
            name:Jagiellonian University Medical College
            address:
               name:Department of Oncology, Jagiellonian University Medical College, Krak贸w, Poland
               type:PostalAddress
            type:Organization
      name:Diana Hodorowicz-Zaniewska
      affiliation:
            name:Jagiellonian University Medical College
            address:
               name:Department of General, Oncological, and Gastrointestinal Surgery, Jagiellonian University Medical College, Krak贸w, Poland
               type:PostalAddress
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      affiliation:
            name:Jagiellonian University Medical College
            address:
               name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
      name:2nd Department of Internal Medicine, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of Oncology, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of General, Oncological, and Gastrointestinal Surgery, Jagiellonian University Medical College, Krak贸w, Poland
      name:Department of Pathomorphology, Jagiellonian University Medical College, Krak贸w, Poland

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