Abduljabbar Rezvan, Negm Ola H, Lai Chun-Fui, Jerjees Dena A, Al-Kaabi Methaq, Hamed Mohamed R, Tighe Patrick J, Buluwela Lakjaya, Mukherjee Abhik, Green Andrew R, Ali Simak, Rakha Emad A, Ellis Ian O
Division of Cancer and Stem Cell, Department of Histopathology, The University of Nottingham, City Hospital Campus, Nottingham, UK,
Breast Cancer Res Treat. 2015 Apr;150(2):335-46. doi: 10.1007/s10549-015-3335-1. Epub 2015 Mar 12.
The glucocorticoid receptor (GR) is a member of the nuclear receptor superfamily of transcription factors, which exerts anti-proliferative and anti-apoptotic activities. The GR is expressed in a large proportion of breast cancer (BC) although levels generally decrease during cancer progression. This study aimed to determine the clinical and biological significance of GR expression using a large series of early-stage BC with long-term follow-up and BC cell lines. Immunohistochemistry was used to assess the expression of GR in 999 cases of primary invasive BC prepared as tissue microarrays. Reverse phase protein microarray was used to assess the expression of GR in MCF7 and MDA-MB-231 cell lines. Nuclear expression of GR was observed in 61.6 % of breast tumours and was associated with features of good prognosis including smaller tumour size and lower grade with less pleomorphism and low mitotic count. GR expression was positively correlated with expression of oestrogen (ER) and progesterone receptors. In ER-positive tumours, GR was associated with other features of favourable outcome including FOXA1, GATA3 and BEX1 expression, while low GR expression was associated with high Ki67, p53 and CD71 expression. GR expression is associated with features of good outcome but does not provide prognostic information independent of size, stage and grade. Understanding the receptor and its effects on BC behaviour is essential for avoiding any unwanted effects from the use of glucocorticoids in routine oncology practice.
糖皮质激素受体(GR)是转录因子核受体超家族的成员,具有抗增殖和抗凋亡活性。GR在大部分乳腺癌(BC)中表达,尽管在癌症进展过程中其水平通常会下降。本研究旨在通过对大量具有长期随访的早期BC病例和BC细胞系进行研究,确定GR表达的临床和生物学意义。采用免疫组织化学方法评估999例制备成组织芯片的原发性浸润性BC中GR的表达。采用反相蛋白质芯片技术评估MCF7和MDA-MB-231细胞系中GR的表达。在61.6%的乳腺肿瘤中观察到GR的核表达,其与预后良好的特征相关,包括肿瘤较小、分级较低、多形性较少和有丝分裂计数较低。GR表达与雌激素(ER)和孕激素受体的表达呈正相关。在ER阳性肿瘤中,GR与其他有利预后特征相关,包括FOXA1、GATA3和BEX1表达,而GR低表达与高Ki67、p53和CD71表达相关。GR表达与良好预后特征相关,但不能提供独立于肿瘤大小、分期和分级的预后信息。了解该受体及其对BC行为的影响对于避免在常规肿瘤学实践中使用糖皮质激素产生任何不良影响至关重要。