| Literature DB >> 19231155 |
Ioannis Mylonas1, Silvia Worbs2, Naim Shabani3, Christina Kuhn2, Susanne Kunze2, Sandra Schulze2, Darius Dian2, Andrea Gingelmaier2, Christian Schindlbeck2, Ansgar Brüning2, Harald Sommer2, Udo Jeschke2, Klaus Friese2.
Abstract
Inhibins are dimeric glycoproteins, composed of an alpha-subunit (inhibin-alpha) and one of two possible beta-subunits (betaA or betaB), with substantial roles in human reproduction and in endocrine-responsive tumours. The aims of this study were to determine the distribution of inhibin-alpha, -betaA and -betaB subunits in malignant human endometrial tissue and the assessment of an association with specific clinicopathologic tumour features and clinical outcome. A series of 302 endometrial cancer tissue samples were immunohistochemically analysed with monoclonal antibodies against inhibin subunits. The inhibin-alpha subunit showed a significant association with histological grading, surgical staging, lymph node status and diabetes in patients with endometrial cancer. Interestingly, loss of inhibin-alpha expression resulted in a poorer survival of endometrial cancer patients. Additionally, survival analysis demonstrated that inhibin-alpha immunoreactivity was an independent prognostic factor for progression-free survival, cause-specific survival as well as for overall survival. In contrast, although inhibin-betaA- and -betaB subunits showed a significant association between endometrial histological subtypes and histological grading, both subunits were not found to be associated with survival in endometrial cancer patients. Therefore, inhibin-alpha immunostaining might be used as a simple and efficient marker to identify high-risk patients leading to the selection of patients for an aggressive adjuvant therapy.Entities:
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Year: 2009 PMID: 19231155 DOI: 10.1016/j.ejca.2009.01.008
Source DB: PubMed Journal: Eur J Cancer ISSN: 0959-8049 Impact factor: 9.162