Comparative immunohistochemical analysis of aurora-A and aurora-B expression in human glioblastomas. Associations with proliferative activity and clinicopathological features |
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Authors: | Vassilis Samaras Angeliki Stamatelli Efstathios Samaras Christos Arnaoutoglou Marianthi Arnaoutoglou Ioanna Stergiou Paraskevi Konstantopoulou Vassilis Varsos Andreas Karameris Calypso Barbatis |
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Affiliation: | 1. Department of Histology and Embryology, National and Kapodistrian University of Athens, Medical School, 75 Mikras Asias, 11527 Goudi, Athens, Greece;2. 1st Department of Pathology, National and Kapodistrian University of Athens, Medical School, Athens, Greece;3. Department of Neurosurgery, Hellenic Red Cross Hospital, Athens, Greece;4. Department of Cytopathology, Evangelismos General Hospital, Athens, Greece;5. 1st Department of Neurology, Aristotle University of Thessaloniki, Thessaloniki, Greece;6. Department of Radiology, General Hospital of Lamia, Lamia, Greece;g Department of Pathology, 417 VA Hospital, Athens, Greece;h Department of Pathology, Hellenic Red Cross Hospital, Athens, Greece |
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Abstract: | In the present study, we carried out a comparative immunohistochemical analysis of aurora-A and aurora-B expression in 40 patients with primary glioblastomas, and attempted to identify any associations with Ki-67 index and the patients’ clinical features. The impact of various treatment modalities and proliferative activity on patient outcome was also assessed.Immunohistochemistry was carried out using formalin-fixed and paraffin-embedded tissue sections.Aurora-A expression was higher in tumors with high Ki-67 expression (p=0.01) and was positively, though marginally, related to aurora-B expression (p=0.085). Aurora-B expression was not linked to Ki-67 expression (p=0.182). Lower aurora-A immunohistochemical expression, chemotherapy administration, and tumor localization in one lobe of the brain implied a greater probability of patient survival in univariate analysis (p=0.044, p=0.008, p=0.041, respectively). Ki-67 and aurora-B immunoreactivities were not associated with patient survival (p=0.918 and p=0.539, respectively).To our knowledge, for the first time, the association between aurora-A and aurora-B expression, the correlation of aurora-A with Ki-67 index, and the prognostic impact of aurora-A expression were assessed in glioblastomas. Although we addressed a prognostic connotation of aurora-A, we presume that aurora-A and aurora-B play a complicated role within glioblastomas. Further examinations of larger series are required, so that definite conclusions can be drawn. |
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Keywords: | Glioblastoma Aurora-A Aurora-B Chemotherapy Prognosis |
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