雌激素受体-β在正常乳腺和肿瘤组织中的表达及其变异

K. Kim, M. Heo, Seung Il Kim, Byeong-Woo Park
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引用次数: 0

摘要

目的:自雌激素受体-β (estrogen receptor-β, ERβ)被发现以来,已鉴定出5种雌激素受体-β的c端变异。本研究旨在探讨ER-β及其剪接变体在正常和恶性乳腺组织中的表达模式和临床意义。方法:采用逆转录聚合酶链反应(RT-PCR)检测50对正常和癌组织中ER-α和ER-β及其5个剪接变体(β1、β2、β3、β4、β5)的表达水平。我们使用Tina version 2.10 (Raytest,德国)测量RT-PCR产物的密度。首先比较了ER-α和ER-β及其5种剪接变体的发生率和强度。然后分析ER-β mRNA剪接变异体的表达、免疫组化染色测定的ER-α蛋白表达和患者的绝经状态。采用卡方检验和配对样本t检验进行统计分析。当p值小于0.05时,认为差异显著。结果:正常乳腺和癌组织中ER-β mRNA变异表达情况为:ER-β2(100%/100%)、ER-β4(76%/74%)、ER-β5(32%/58%)、ER-β1(14%/16%)。未检测到ER-β3。在强度方面,我们观察到与相应的正常乳腺组织相比,乳腺癌中ER-β2的mRNA表达水平显著降低(P<0.001), ER-β5的mRNA表达水平显著升高(P=0.004)。与相应的正常组织相比,ER-α-阳性、50岁以上(P=0.01)、50岁以下(P=0.04)患者癌组织中ER-β2表达均显著降低(P<0.001),而ER-α-阴性患者则无显著降低(P=0.48)。ER-α-阳性患者ER-β4明显降低(P=0.004),年龄≥50岁患者ER-β4明显降低(P=0.07)。ER-β5仅在50岁以上患者中有显著升高(P=0.04)。结论:癌组织中ER-α mRNA表达明显高于正常组织,ER-β mRNA表达明显低于正常组织。在ER-β变异形式中,ER-β2在正常和恶性乳腺组织中均占主导地位,ER-β4、ER-β5和ER-β1在乳腺组织中依次表达,而ER-β3在乳腺组织中不表达。ER-β2和ER-β4的表达减少在肿瘤组织中表现突出,尤其是在ER-α阳性肿瘤中,这提示ER-β2和ER-β4可能在乳腺癌发生过程中具有调节作用。进一步的研究来验证ER-β变异的作用是必要的。(韩国乳腺癌学会杂志2003;6:161-167)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression of Estrogen Receptor-β and Its Variants in Normal Mammary and Tumor Tissues
Purpose: Since the discovery of estrogen receptor-β (ERβ), five C-terminal variants of ER-β were identified. We designed this study to investigate the pattern and clinical implications of ER-β and its splicing variants expression in normal and malignant mammary tissues. Methods: Using reverse transcription polymerase chain reaction (RT-PCR), we examined the expression levels of ER-α and ER-β and its five splicing variants (β1, β2, β3, β4, β5) in 50 paired normal and cancer tissues. We measured the densities of RT-PCR products using Tina version 2.10 (Raytest, Germany). Firstly, the incidence and intensity of ER-α and ER-β and its five splicing variants were compared. Then the expression of ER-β mRNA splicing variants was also analyzed with regard to the ER-α protein expression measured by immuno-histochemical staining and the menopausal status of the patients. Chi-square test and paired samples t-test were used for statistical analysis. Differences were considered to be significant with a p-value of less than 0.05. Results: The expression of ER-β mRNA variants in normal breast and cancer tissues were as follows: ER-β2 (100%/100%), ER-β4 (76%/74%), ER-β5 (32%/58%), and ER-β1 (14%/16%). ER-β3 was not detected at all. In terms of intensity, we observed a significant decrease of ER-β2 (P<0.001) and an increase of ER-β5 (P=0.004) in the mRNA expression levels among breast cancers compared to the corresponding normal breast tissues. Compared to the corresponding normal tissues, a significant decrease of ER-β2 in cancer tissues was observed in patients with ER-α-positive (P<0.001), with age over 50 (P=0.01), and under 50 (P=0.04) as well, but not in patients with ER-α-negative (P=0.48). ER-β4 also significantly decreased in patients with ER-α-positive (P=0.004) and with age over 50 (P=0.07). ER-β5 showed a significant increment only in patient aged over 50 (P=0.04). Conclusion: ER-α mRNA expression significantly increases but ER-β mRNA expression decreases in the cancer tissues compared to the corresponding normal tissues. Among ER-β variant forms, ER-β2 is predominant in both normal and malignant mammary tissues and ER-β4, ER-β5, and ER-β1 in descending order but ER-β3 does not express in mammary tissues. The decrease of ER-β2 and ER-β4 expression is prominent in cancer tissue especially in ER-α-positive cancers, which suggests that ER-β2 and ER-β4 may possess a regulatory function in mammary carcinogenesis. Further investigations to verify the roles of ER-β variants are mandatory. (Journal of Korean Breast Cancer Society 2003;6:161-167)
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