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cells, tumors, cdcd, breast, cancer, tumor, expression, pubmed, article, google, scholar, gene, basallike, phenotype, cas, positive, status, cell, staining, srher, table, data, clinical, correlation, receptor, subgroups, analysis, presence, subtypes, patients, res, stem, detected, brca, study, proportion, survival, central, human, characteristics, signature, subtype, research, subgroup, genes, lund, colleagues, size, markers, results,

Topics {✒️}

estrogen-receptor-negative breast cancers er-negative stem/progenitor cells cd44+/cd24−/ck+/cd45− cells article download pdf stem/progenitor cell properties eralpha-negative breast carcinoma distant disease-free survival intra-tumoral heterogeneity resulting human breast carcinoma paraffin-embedded tumor tissue cell-based liquid biopsy brca1-defective breast tumors putative tumor-initiating cells invasive breast cancers cytokeratin clone ae1/ae3 human breast tumours rijn van de her2/neu-overexpressing phenotypes swedish research council invasive breast carcinoma human breast tumors stem/progenitor cells clinical cancer research cancer stem cells maintain tumor growth disease-free survival immunohistochemistry-based pilot study related subjects open-source system invasive breast carcinomas swedish cancer society greater stem cell stem cell biology predominantly cd44+/cd24- cells natl cancer inst cd44+/cd24- tumor cells cd44-/cd24+ tumor cells top-ranked overexpressed genes breast cancer cells full size table tumour progression breast cancer res gruvberger-saal sk privacy choices/manage cookies cd44+/cd24-/low cells breast cancer samples strategic research breast tumor heterogeneity expressed cd44+/cd24- cells breast cancer patients

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         headline:The CD44+/CD24-phenotype is enriched in basal-like breast tumors
         description:Human breast tumors are heterogeneous and consist of phenotypically diverse cells. Breast cancer cells with a CD44+/CD24- phenotype have been suggested to have tumor-initiating properties with stem cell-like and invasive features, although it is unclear whether their presence within a tumor has clinical implications. There is also a large heterogeneity between tumors, illustrated by reproducible stratification into various subtypes based on gene expression profiles or histopathological features. We have explored the prevalence of cells with different CD44/CD24 phenotypes within breast cancer subtypes. Double-staining immunohistochemistry was used to quantify CD44 and CD24 expression in 240 human breast tumors for which information on other tumor markers and clinical characteristics was available. Gene expression data were also accessible for a cohort of the material. A considerable heterogeneity in CD44 and CD24 expression was seen both between and within tumors. A complete lack of both proteins was evident in 35% of the tumors, while 13% contained cells of more than one of the CD44+/CD24-, CD44-/CD24+ and CD44+/CD24+ phenotypes. CD44+/CD24- cells were detected in 31% of the tumors, ranging in proportion from only a few to close to 100% of tumor cells. The CD44+/CD24- phenotype was most common in the basal-like subgroup – characterized as negative for the estrogen and progesterone receptors as well as for HER2, and as positive for cytokeratin 5/14 and/or epidermal growth factor receptor, and particularly common in BRCA1 hereditary tumors, of which 94% contained CD44+/CD24- cells. The CD44+/CD24- phenotype was surprisingly scarce in HER2+ tumors, which had a predominantly CD24+ status. A CD44+/CD24- gene expression signature was generated, which included CD44 and α6-integrin (CD49f) among the top-ranked overexpressed genes. We demonstrate an association between basal-like and particularly BRCA1 hereditary breast cancer and the presence of CD44+/CD24- cells. Not all basal-like tumors and very few HER2+ tumors, however, contain CD44+/CD24- cells, emphasizing that a putative tumorigenic ability may not be confined to cells of this phenotype and that other breast cancer stem cell markers remain to be identified.
         datePublished:2008-06-17T00:00:00Z
         dateModified:2008-06-17T00:00:00Z
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            Epidermal Growth Factor Receptor
            Human Breast Tumor
            Breast Cancer Subgroup
            BRCA1 Germline Mutation Carrier
            Distinct Genetic Profile
            Cancer Research
            Oncology
            Surgical Oncology
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      headline:The CD44+/CD24-phenotype is enriched in basal-like breast tumors
      description:Human breast tumors are heterogeneous and consist of phenotypically diverse cells. Breast cancer cells with a CD44+/CD24- phenotype have been suggested to have tumor-initiating properties with stem cell-like and invasive features, although it is unclear whether their presence within a tumor has clinical implications. There is also a large heterogeneity between tumors, illustrated by reproducible stratification into various subtypes based on gene expression profiles or histopathological features. We have explored the prevalence of cells with different CD44/CD24 phenotypes within breast cancer subtypes. Double-staining immunohistochemistry was used to quantify CD44 and CD24 expression in 240 human breast tumors for which information on other tumor markers and clinical characteristics was available. Gene expression data were also accessible for a cohort of the material. A considerable heterogeneity in CD44 and CD24 expression was seen both between and within tumors. A complete lack of both proteins was evident in 35% of the tumors, while 13% contained cells of more than one of the CD44+/CD24-, CD44-/CD24+ and CD44+/CD24+ phenotypes. CD44+/CD24- cells were detected in 31% of the tumors, ranging in proportion from only a few to close to 100% of tumor cells. The CD44+/CD24- phenotype was most common in the basal-like subgroup – characterized as negative for the estrogen and progesterone receptors as well as for HER2, and as positive for cytokeratin 5/14 and/or epidermal growth factor receptor, and particularly common in BRCA1 hereditary tumors, of which 94% contained CD44+/CD24- cells. The CD44+/CD24- phenotype was surprisingly scarce in HER2+ tumors, which had a predominantly CD24+ status. A CD44+/CD24- gene expression signature was generated, which included CD44 and α6-integrin (CD49f) among the top-ranked overexpressed genes. We demonstrate an association between basal-like and particularly BRCA1 hereditary breast cancer and the presence of CD44+/CD24- cells. Not all basal-like tumors and very few HER2+ tumors, however, contain CD44+/CD24- cells, emphasizing that a putative tumorigenic ability may not be confined to cells of this phenotype and that other breast cancer stem cell markers remain to be identified.
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      dateModified:2008-06-17T00:00:00Z
      pageStart:1
      pageEnd:12
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      keywords:
         Epidermal Growth Factor Receptor
         Human Breast Tumor
         Breast Cancer Subgroup
         BRCA1 Germline Mutation Carrier
         Distinct Genetic Profile
         Cancer Research
         Oncology
         Surgical Oncology
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            name:CREATE Health Strategic Centre for Clinical Cancer Research
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      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:CREATE Health Strategic Centre for Clinical Cancer Research, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Institute for Cancer Genetics, Columbia University, New York, USA
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Institute for Cancer Genetics, Columbia University, New York, USA
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Department of Pathology, Clinical Sciences, Lund University, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:CREATE Health Strategic Centre for Clinical Cancer Research, Lund, Sweden
      name:Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund, Sweden
      name:Department of Oncology, Clinical Sciences, Lund University, Lund, Sweden
      name:CREATE Health Strategic Centre for Clinical Cancer Research, Lund, Sweden
      name:Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund, Sweden

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