GPER-1 expression is associated with a decreased response rate to primary tamoxifen therapy of breast cancer patients

被引:19
作者
Ignatov, Tanja [1 ,2 ]
Treeck, Oliver [1 ]
Kalinski, Thomas [3 ,4 ]
Ortmann, Olaf [1 ]
Ignatov, Atanas [1 ]
机构
[1] Univ Med Ctr, Dept Gynecol, Obstet, Landshuter Str. 65, DE-93053 Regensburg, Germany
[2] Reprod Ctr, KITZ, Regensburg, Germany
[3] Guericke Univ, Dept Pathol, Magdeburg, Germany
[4] Pathol Hamburg, Hamburg, Germany
关键词
GPER-1; GPR30; Breast cancer; Tamoxifen resistance; COUPLED ESTROGEN-RECEPTOR; TUMOR-SUPPRESSOR; GPR30; PROLIFERATION; ACTIVATION; MEMBRANE;
D O I
10.1007/s00404-019-05384-6
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Purpose Endocrine therapies using tamoxifen and/or aromatase inhibitors are important therapeutic options for the targeted treatment of hormone-responsive breast cancer. In addition to nuclear estrogen receptors ER alpha and beta, G-protein-coupled estrogen receptor GPER-1 is a third receptor-mediating estrogen effects in breast cancer cells. The aim of this study was to examine to what extent GPER-1 expression might affect the efficacy of primary endocrine treatment of breast cancer. Methods GPER-1 expression was determined in tissue samples from patients with early breast cancer by means of immunohistochemistry and a GPER-1 score of >= 3 was considered to be positive. In a total of 165 patients, the response to a primary therapy with tamoxifen (TAM) or aromatase inhibitors (AI) was assessed by ultrasound imaging for up to 6 months. The primary endpoint of this study was the response to treatment evaluated by RECIST 1.1 criteria. Results GPER-1 expression was observed in 127 (77.0%) out of 165 cases. Based on GPER-1 expression and the type of endocrine treatment, the patients were divided into 4 groups: GPER-1 negative/TAM (12.1%), GPER-1 negative/AI (10.9%), GPER-1 positive/TAM (44.8%), and GPER-1 positive/AI (32.1%). The groups were well balanced regarding different clinical and pathological factors. After 4 and 6 months of treatment, a high level of stable disease or progressive disease was observed in the GPER-1 positive/TAM group only (p < 0.0001), whereas in the other three groups of patients, the most common objective response was classified as partial response. We observed a continuous reduction of mean tumor size in patients treated with aromatase inhibitors irrespective of the GPER-1 status and in GPER-1 negative patients treated with TAM. In contrast, in GPER-1 positive patients treated with TAM, a reduction of mean tumor size was observed only in the first 2 months after beginning of treatment. Four and six months after start of treatment, no reduction, but even a slight increase of tumor size was observed in this patients group. Conclusions GPER-1 expression is significantly associated with a reduced effect of primary treatment with tamoxifen in breast cancer patients.
引用
收藏
页码:565 / 571
页数:7
相关论文
共 21 条
[1]   The G Protein-Coupled Receptor GPR30 Inhibits Proliferation of Estrogen Receptor-Positive Breast Cancer Cells [J].
Ariazi, Eric A. ;
Brailoiu, Eugen ;
Yerrum, Smitha ;
Shupp, Heather A. ;
Slifker, Michael J. ;
Cunliffe, Heather E. ;
Black, Michael A. ;
Donato, Anne L. ;
Arterburn, Jeffrey B. ;
Oprea, Tudor I. ;
Prossnitz, Eric R. ;
Dun, Nae J. ;
Jordan, V. Craig .
CANCER RESEARCH, 2010, 70 (03) :1184-1194
[2]   G Protein-Coupled Estrogen Receptor Is Apoptotic and Correlates with Increased Distant Disease-Free Survival of Estrogen Receptor-Positive Breast Cancer Patients [J].
Broselid, Stefan ;
Cheng, Benxu ;
Sjostrom, Martin ;
Lovgren, Kristina ;
Klug-De Santiago, Heather L. P. ;
Belting, Mattias ;
Jirstrom, Karin ;
Malmstrom, Per ;
Olde, Bjorn ;
Bendahl, Par-Ola ;
Hartman, Linda ;
Ferno, Marten ;
Leeb-Lundberg, L. M. Fredrik .
CLINICAL CANCER RESEARCH, 2013, 19 (07) :1681-1692
[3]   Activation of GPR30 inhibits the growth of prostate cancer cells through sustained activation of Erk1/2, c-jun/c-fos-dependent upregulation of p21, and induction of G2 cell-cycle arrest [J].
Chan, Q. K. Y. ;
Lam, H-M ;
Ng, C-F ;
Lee, A. Y. Y. ;
Chan, E. S. Y. ;
Ng, H-K ;
Ho, S-M ;
Lau, K-M .
CELL DEATH AND DIFFERENTIATION, 2010, 17 (09) :1511-1523
[4]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[5]   Meta-analysis of the association of breast cancer subtype and pathologic complete response to neoadjuvant chemotherapy [J].
Houssami, Nehmat ;
Macaskill, Petra ;
von Minckwitz, Gunter ;
Marinovich, Michael L. ;
Mamounas, Eleftherios .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (18) :3342-3354
[6]   G-protein-coupled estrogen receptor GPR30 and tamoxifen resistance in breast cancer [J].
Ignatov, Atanas ;
Ignatov, Tanja ;
Weissenborn, Christine ;
Eggemann, Holm ;
Bischoff, Joachim ;
Semczuk, Andrzej ;
Roessner, Albert ;
Costa, Serban Dan ;
Kalinski, Thomas .
BREAST CANCER RESEARCH AND TREATMENT, 2011, 128 (02) :457-466
[7]   Role of GPR30 in the mechanisms of tamoxifen resistance in breast cancer MCF-7 cells [J].
Ignatov, Atanas ;
Ignatov, Tanja ;
Roessner, Albert ;
Costa, Serban Dan ;
Kalinski, Thomas .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 123 (01) :87-96
[8]   G-protein-coupled estrogen receptor GPER-1 expression in hormone receptor-positive breast cancer is associated with poor benefit of tamoxifen [J].
Ignatov, Tanja ;
Claus, Maria ;
Nass, Norbert ;
Haybaeck, Johannes ;
Seifert, Bernd ;
Kalinski, Thomas ;
Ortmann, Olaf ;
Ignatov, Atanas .
BREAST CANCER RESEARCH AND TREATMENT, 2019, 174 (01) :121-127
[9]   GPER-1 acts as a tumor suppressor in ovarian cancer [J].
Ignatov, Tanja ;
Modl, Saskia ;
Thulig, Maike ;
Weissenborn, Christine ;
Treeck, Oliver ;
Ortmann, Olaf ;
Zenclussen, A. C. ;
Costa, Serban Dan ;
Kalinski, Thomas ;
Ignatov, Atanas .
JOURNAL OF OVARIAN RESEARCH, 2013, 6
[10]   GPER-1 Expression Decreases During Breast Cancer Tumorigenesis [J].
Ignatov, Tanja ;
Weissenborn, Christine ;
Poehlmann, Angela ;
Lemke, Antje ;
Semczuk, Andrzej ;
Roessner, Albert ;
Costa, Serban Dan ;
Kalinski, Thomas ;
Ignatov, Atanas .
CANCER INVESTIGATION, 2013, 31 (05) :309-315