Death domain-associated protein (DAXX) expression is associated with poor survival in metastatic high-grade serous carcinoma

被引:0
|
作者
Ben Davidson
Erin McFadden
Arild Holth
Marta Brunetti
Vivi Ann Flørenes
机构
[1] Oslo University Hospital,Department of Pathology, Norwegian Radium Hospital
[2] University of Oslo,Faculty of Medicine, Institute of Clinical Medicine
[3] Oslo University Hospital,Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital
来源
Virchows Archiv | 2020年 / 477卷
关键词
DAXX; ATRX; Immunohistochemistry; Western blotting; High-grade serous carcinoma; Effusion;
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摘要
The objective of this study was to analyze the expression and clinical role of mitosis regulators α-thalassemia/mental retardation syndrome X-linked (ATRX) and death-domain-associated protein (DAXX) in metastatic high-grade serous carcinoma (HGSC). ATRX and DAXX protein expression by immunohistochemistry was analyzed in 400 HGSC effusions. DAXX expression was additionally studied in 15 cancer cell lines, including 4 ovarian carcinoma lines, and in 81 of the 400 HGSC effusions using Western blotting. ATRX and DAXX were expressed in HGSC cells in 386/400 (96%) and 348/400 (87%) effusions, respectively. Western blotting showed DAXX expression in all 15 cell lines and in 70/81 (86%) HGSC effusions. DAXX expression by immunohistochemistry was higher in pleural compared to peritoneal effusions (p = 0.006) and in post-chemotherapy compared to pre-chemotherapy effusions (p = 0.004), and its expression was significantly associated with poor overall survival in univariate of the entire cohort (p = 0.014), as well as analysis limited to chemo-naïve effusions tapped at diagnosis (p = 0.038). The former association retained its prognostic role in Cox multivariate survival analysis (p = 0.011). ATRX expression was unrelated to clinicopathologic parameters or survival. In conclusion, DAXX is associated with disease progression and could be a prognostic marker in metastatic HGSC. Silencing this molecule may have therapeutic relevance in this cancer.
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页码:857 / 864
页数:7
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