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authors scientific editing privacy choices/manage cookies bmc european economic area androgen receptor expresion ar score values state privacy rights accepting optional cookies 1471-2407 contact manage preferences personal data breast cancer submission enquiries optional cookies data protection essential cookies cookies skip cookies policy privacy policy privacy statement usage analysis social media varying standards clinicopathological characteristics inhibitors distribution 111 breast carcinomas general enquiries preference centre springer nature content choices privacy choice make site function advertising personalisation consent processing parties information change accept published relationship tumors prognosis expression metalloproteases

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         headline:Androgen receptor expresion in breast cancer: Relationship with clinicopathological characteristics of the tumors, prognosis, and expression of metalloproteases and their inhibitors
         description:In the present study we analyze, in patients with breast cancer, the tumor expression of androgen receptors (AR), its relationship with clinicopathological characteristics and with the expression of several matrix metalloproteases (MMPs) and their inhibitors (TIMPs), as well as with prognosis. An immunohistochemical study was performed using tissue microarrays and specific antibodies against AR, MMPs -1, -2, -7, -9, -11, -13, -14, and TIMPs -1, -2 and -3. More than 2,800 determinations on tumor specimens from 111 patients with primary invasive ductal carcinoma of the breast (52 with axillary lymph node metastases and 59 without them) and controls were performed. Staining results were categorized using a score based on the intensity of the staining and a specific software program calculated the percentage of immunostained cells automatically. A total of 83 cases (74.8%) showed a positive immunostaining for AR, but with a wide variation in the staining score values. There were no significant associations between the total immunostaining scores for AR and any clinicopathological parameters. However, score values for MMP-1, -7 and -13, were significantly higher in AR-positive tumors than in AR-negative tumors. Likewise, when we considered the cellular type expressing each factor, we found that AR-positive tumors had a higher percentage of cases positive for MMP-1, -7, -11, and TIMP-2 in their malignant cells, as well as for MMP-1 in intratumoral fibroblasts. On the other hand, multivariate analysis demonstrated that patients with AR-positive tumors have a significant longer overall survival than those with AR-negative breast carcinomas (p = 0.03). Our results confirm that AR are commonly expressed in breast cancer, and are correlated with the expression of some MMPs and TIMP-2. Although we found a specific value of AR expression to be a prognostic indicator in breast cancer, the functional role of AR in these neoplasms is still unclear and further data are needed in order to clarify their biological signification in breast cancer.
         datePublished:2008-05-28T00:00:00Z
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            Tissue Array Block
            Total Immunostaining Score
            Primary Invasive Ductal Carcinoma
            Apocrine Breast Carcinoma
            Cancer Research
            Oncology
            Surgical Oncology
            Health Promotion and Disease Prevention
            Biomedicine
            general
            Medicine/Public Health
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      headline:Androgen receptor expresion in breast cancer: Relationship with clinicopathological characteristics of the tumors, prognosis, and expression of metalloproteases and their inhibitors
      description:In the present study we analyze, in patients with breast cancer, the tumor expression of androgen receptors (AR), its relationship with clinicopathological characteristics and with the expression of several matrix metalloproteases (MMPs) and their inhibitors (TIMPs), as well as with prognosis. An immunohistochemical study was performed using tissue microarrays and specific antibodies against AR, MMPs -1, -2, -7, -9, -11, -13, -14, and TIMPs -1, -2 and -3. More than 2,800 determinations on tumor specimens from 111 patients with primary invasive ductal carcinoma of the breast (52 with axillary lymph node metastases and 59 without them) and controls were performed. Staining results were categorized using a score based on the intensity of the staining and a specific software program calculated the percentage of immunostained cells automatically. A total of 83 cases (74.8%) showed a positive immunostaining for AR, but with a wide variation in the staining score values. There were no significant associations between the total immunostaining scores for AR and any clinicopathological parameters. However, score values for MMP-1, -7 and -13, were significantly higher in AR-positive tumors than in AR-negative tumors. Likewise, when we considered the cellular type expressing each factor, we found that AR-positive tumors had a higher percentage of cases positive for MMP-1, -7, -11, and TIMP-2 in their malignant cells, as well as for MMP-1 in intratumoral fibroblasts. On the other hand, multivariate analysis demonstrated that patients with AR-positive tumors have a significant longer overall survival than those with AR-negative breast carcinomas (p = 0.03). Our results confirm that AR are commonly expressed in breast cancer, and are correlated with the expression of some MMPs and TIMP-2. Although we found a specific value of AR expression to be a prognostic indicator in breast cancer, the functional role of AR in these neoplasms is still unclear and further data are needed in order to clarify their biological signification in breast cancer.
      datePublished:2008-05-28T00:00:00Z
      dateModified:2008-05-28T00:00:00Z
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         Immunostaining Score
         Tissue Array Block
         Total Immunostaining Score
         Primary Invasive Ductal Carcinoma
         Apocrine Breast Carcinoma
         Cancer Research
         Oncology
         Surgical Oncology
         Health Promotion and Disease Prevention
         Biomedicine
         general
         Medicine/Public Health
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            name:Hospital de Jove
            address:
               name:Servicio de Cirugía General, Hospital de Jove, Gijón, Spain
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain
      name:Servicio de Anatomía Patológica, Hospital de Jove, Gijón, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain
      name:Servicio de Ginecología, Hospital Álvarez Buylla, Mieres, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain
      name:Servicio de Cirugía General, Hospital de Jove, Gijón, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain
      name:Servicio de Ginecología, Hospital de Jove, Gijón, Spain
      name:Unidad de Investigación, Hospital de Jove, Gijón, Spain
      name:Instituto Universitario de Oncología del Principado de Asturias, Oviedo, Spain
      name:Servicio de Cirugía General, Hospital de Jove, Gijón, Spain

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