三阴性乳腺癌患者雌激素受体β的评估

HS Mubisi, MM Farouk, I. Zaki, TA El Fayoiem, A. Ismail
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简介:三阴性乳腺癌(TNBC)被定义为缺乏雌激素受体α (ERα)、孕激素受体和人表皮生长因子受体的表达,是一种侵袭性乳腺癌亚型,需要寻找新的治疗靶点。约50-80%的TNBC表达雌激素受体β (ERβ)。鉴于ERβ在结构、信号传导和对乳腺癌细胞的抗增殖作用方面与ERα略有不同,ERβ可能是一个可能的治疗靶点。本研究旨在评估埃及女性TNBC患者中ERβ的存在及其与临床病理特征的相关性。材料与方法:本研究为回顾性分析。以下数据从患者档案中检索并记录:年龄、肿瘤大小、淋巴结转移和分期。对经免疫组化证实为TNBC的患者石蜡块进行ERβ、CK5/6和Ki 67的免疫组化染色。结果:80%的病例ERβ阳性(n=32/40)。ERβ与年龄(rs = -0.473, P = 0.002, n =40)、肿瘤大小(rs = -0.471, P = 0.007, n =40)、淋巴结(rs = -0.365, P = 0.021, n =40)、分期(rs = -0.468, P = 0.002, n =40)显著相关。ERβ与Ki-67和基础表型标志物CK5/6之间没有相关性。8例无ERβ的患者均为侵袭性疾病。4例接受新辅助化疗,腋窝淋巴结病理完全缓解最小或无完全缓解,2例出现前期转移性疾病,另外2例局部复发,肿瘤分子表型从腔内亚型转变为TNBC。结论:ERβ在TNBC中有表达。它可能有潜力成为TNBC的治疗靶点。
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Assessment of Estrogen Receptor Beta in Patients with Triple Negative Breast Cancer
Introduction: Triple negative breast cancer (TNBC), defined as lacking the expression of estrogen receptor alpha (ERα), progesterone receptor and human epidermal growth factor receptor is an aggressive breast cancer subtype for which there is a need to identify new therapeutic targets. About 50-80% of TNBC express Estrogen Receptor Beta (ERβ). Given its slight differences from ERα in terms of structure, signaling and its anti-proliferative effects on breast cancer cells, ERβ may be a possible therapeutic target. This study sought to assess the presence of ERβ and its correlation with the clinico-pathological features among the Egyptian females with TNBC. Material and Methods: The study was a retrospective analysis. The following data was retrieved from patient’s files and recorded: age, tumor size, lymph nodes metastasis, and stage. Paraffin blocks for patients confirmed by IHC to be TNBC were subjected to immunohistochemical staining for ERβ, CK5/6, and Ki 67. Results: ERβ was positive in 80% of cases (n=32/40). ERβ significantly correlated with Age (rs = -0.473, P = 0.002, n = 40), Tumor size (rs = -0.471, P = 0.007, n = 40), Lymph nodes (rs = -0.365, P = 0.021, n =40), and Stage (rs = -0.468, P = 0.002, n = 40). There was no correlation between ERβ with Ki-67 and CK5/6 a marker of the basal phenotype. All 8 patients without ERβ had an aggressive disease. 4 received neoadjuvant chemotherapy with minimum or no pathologic complete response in the axillary lymph nodes, 2 presented with upfront metastatic disease while the other 2 were cases of local recurrence with a change in the molecular phenotype of the tumor from luminal subtype to TNBC. Conclusion: This study shows ERβ expression occurs in TNBC. It may have the potential to become a therapeutic target for TNBC.
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