The impact of G protein-coupled oestrogen receptor 1 on male breast cancer: a retrospective analysis

被引:1
|
作者
Maiwald, Jan-Hendrik [1 ]
Sprung, Susanne [2 ]
Czapiewski, Piotr [1 ,3 ]
Lessel, Wiebke [1 ]
Scherping, Anna [1 ]
Schomburg, Dirk [4 ]
Plaumann, Markus [4 ]
Tomasik, Bartlomiej [5 ,6 ]
Behre, Gerhard [7 ]
Haybaeck, Johannes [1 ,2 ,8 ,9 ]
Ignatov, Atanas [10 ]
Eggemann, Holm [11 ]
Nass, Norbert [1 ,7 ]
机构
[1] Otto von Guericke Univ, Dept Pathol, 44 Leipziger St, D-39120 Magdeburg, Germany
[2] Med Univ Innsbruck, Inst Pathol Neuropathol & Mol Pathol, Innsbruck, Austria
[3] Dessau Med Ctr, Dept Pathol, Dessau, Germany
[4] Otto von Guericke Univ, Inst Biometr & Med Informat, Magdeburg, Germany
[5] Med Univ Lodz, Dept Biostat & Translat Med, Lodz, Poland
[6] Dana Farber Canc Inst, Dept Radiat Oncol, Boston, MA 02115 USA
[7] Dessau Med Ctr, Clin Internal Med 1, Dessau, Germany
[8] Med Univ Graz, Diagnost & Res Ctr Mol Biomed, Inst Pathol, Graz, Austria
[9] Ctr Biomarker Res Med, Graz, Austria
[10] Otto von Guericke Univ, Dept Obstet & Gynaecol, Magdeburg, Germany
[11] Hosp Magdeburg GmbH, Dept Obstet & Gynaecol, Magdeburg, Germany
来源
关键词
male breast cancer; MBC; survival analysis; GPER-1; GPR30; OS; RFS; TUMOR-SUPPRESSOR; GPER FUNCTIONS; RISK-FACTORS; STATISTICS; DIAGNOSIS; MEMBRANE; GPR30;
D O I
10.5114/wo.2021.110010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The G protein-coupled oestrogen receptor 1 (GPER-1) is a potential prognostic marker in breast cancer. However, its role in male breast cancer (MBC) is still unknown. This study evaluates the expression of GPER-1 in MBC samples and correlates these data with clinical and pathological parameters including patients' survival. Material and methods: For this retrospective analysis of a prospectively maintained cohort of patients with MBC, we examined 161 specimens for GPER-1 expression using immunohistochemistry. An immunoreactive score (IRS) was calculated based on staining intensity and the percentage of positive tumour cells. Then, we correlated GPER-1 IRS with clinical and pathological parameters, and overall and relapse-free survival. Results: About 40% of MBC samples were positive for GPER-1 expression (IRS >= 4). There was no significant correlation with clinicopathological parameters, such as hormone receptor status or grading. However, a statistical trend was observed for tumour size (>= 2 cm, p = 0.093). Kaplan-Meier survival analysis revealed no significant correlation with relapse-free survival. However, there was a significant correlation with overall survival, but when we adjusted the log-rank p-value to compensate for the cut-off point optimization method, it rose above 0.1. Additionally, GPER-1-positive patients were older at diagnosis. When adjusted for age by multivariable Cox regression analysis, the significance of GPER-1 status for survival was further reduced. Conclusions: We found no significant prognostic value of GPER-1 in this MBC cohort as anticipated from studies on female BC. Future studies with higher sample size are needed to further verify a potential sex-specific role of GPER-1.
引用
收藏
页码:204 / 212
页数:9
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