Lee Lisa M J, Cao Jiang, Deng Hao, Chen Ping, Gatalica Zoran, Wang Zhao-Yi
Department of Pathology, Creighton University Medical School, Omaha, NE 68178, USA.
Anticancer Res. 2008 Jan-Feb;28(1B):479-83.
The status of estrogen receptor-alpha (ER-alpha) expression is one of the most important diagnostic and prognostic factors of breast cancer. ER-alpha is a 66-kDa, ligand-induced transcription factor, characteristically detected in the cell nucleus by immunohistochemistry (IHC) in breast cancer specimens. Recently, we identified and cloned a 36-kDa novel variant of ER-alpha, ER-alpha36, which lacks both transactivation domains and functions as a dominant-negative effector of transactivation activities of the full-length ER-alpha (ER-alpha66) and ER-beta. ER-alpha36 primarily localizes to the cytoplasm and plasma membrane, and responds to both estrogens and antiestrogens by transducing membrane-initiated signaling cascades, stimulating proliferation and possibly contributing to a more aggressive phenotype in breast carcinomas. ER-alpha36 is expressed in established ER-positive and -negative breast cancer cell lines. However, its expression and localization in breast cancer specimens have not been evaluated. As ER-alpha36 may play important roles in breast cancer tumorigenesis, it is of clinical importance to examine the expression pattern of ER-alpha36, in addition to that of ER-alpha66, for more comprehensive molecular profiling of breast carcinomas.
Thirty-one breast cancer patient tissues were evaluated for ER-alpha36 and ER-alpha66 protein expression status by IHC and six additional patient tissue samples were analyzed by Western blot analysis using antibodies specific to ER-alpha66 or ER-alpha36.
Our experiments reveal a cytoplasmic and plasma-membrane-associated expression pattern of ER-alpha36 in both ER-alpha66-positive and -negative breast cancer samples. Furthermore, ER-alpha36 expression appears to be associated with decreasing nuclear and/or cytoplasmic ER-alpha66 expression, suggesting its potential use as a diagnostic and prognostic marker.
ER-alpha36 is a novel isoform of ER-alpha, frequently expressed in ER-alpha66-negative cancers, whose detection may provide additional information for better diagnosis and prognosis.
雌激素受体α(ER-α)的表达状态是乳腺癌最重要的诊断和预后因素之一。ER-α是一种66 kDa的配体诱导转录因子,在乳腺癌标本中通过免疫组织化学(IHC)可在细胞核中特异性检测到。最近,我们鉴定并克隆了一种36 kDa的新型ER-α变体ER-α36,它缺乏两个反式激活结构域,并作为全长ER-α(ER-α66)和ER-β反式激活活性的显性负效应物发挥作用。ER-α36主要定位于细胞质和质膜,通过转导膜起始的信号级联反应对雌激素和抗雌激素作出反应,刺激增殖,并可能导致乳腺癌更具侵袭性的表型。ER-α36在已建立的ER阳性和阴性乳腺癌细胞系中均有表达。然而,其在乳腺癌标本中的表达和定位尚未得到评估。由于ER-α36可能在乳腺癌发生中起重要作用,除了检测ER-α66的表达模式外,检测ER-α36的表达模式对于更全面地分析乳腺癌的分子特征具有临床重要性。
通过免疫组织化学评估31例乳腺癌患者组织中ER-α36和ER-α66蛋白的表达状态,并使用针对ER-α66或ER-α36的特异性抗体通过蛋白质印迹分析对另外6例患者组织样本进行分析。
我们的实验揭示了ER-α36在ER-α66阳性和阴性乳腺癌样本中与细胞质和质膜相关的表达模式。此外,ER-α36的表达似乎与细胞核和/或细胞质中ER-α66表达的降低有关,表明其作为诊断和预后标志物的潜在用途。
ER-α36是ER-α的一种新型异构体,在ER-α66阴性癌症中频繁表达,其检测可为更好的诊断和预后提供额外信息。