雌激素受体α rs3798577多态性在乳腺癌风险测定中的作用

P. Kumaladewi, W. Harahap, Bastian Nova, I. Widodo, Ramadhan Karsono, F. Sandra, B. Hernowo
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引用次数: 1

摘要

背景:雌激素与雌激素受体(ER)的相互作用参与了乳腺肿瘤发生的调控和分化。一些ERα多态性,包括ERα rs3798577,被报道与乳腺癌的风险和侵袭性相关,因为该位点被报道为microRNA的靶点,可以进一步调节ERα的表达。因此,本研究旨在揭示ERα SNP rs3798577在乳腺癌患者中的可能作用。方法:从女性患者乳腺切除术后的乳腺癌组织中抽取样本,根据医学和组织病理学记录的完整性进行筛选。采用实时聚合酶链反应(RT-PCR)进行DNA分离,然后进行高分辨率熔融(HRM)分析。然后根据rs3798577 ERα多态性分析核苷酸碱基序列。进行内质网免疫组化检测,根据染色强度和染色细胞百分比进行定量计数。结果:65份样本中,野生型33份,变异型32份。大多数变异型和野生型的ERα百分比>80%。大多数变异型ERα强度中等,而野生型ERα强度较强。变异型ERα组织评分较弱的比例较高(52.2%),野生型ERα组织评分较强的比例较高(52.4%),但差异无统计学意义(p=0.725)。结论:与野生型相比,ERα rs3798577变异型的ERα强度较低,ERα组织评分较弱,提示ERα rs3798577多态性可能在乳腺癌风险判断中发挥作用。关键词:乳腺癌,ERα, rs3798577,多态性,免疫表达
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Estrogen Receptor Alpha rs3798577 Polymorphism in Breast Carcinoma Risk Determination
BACKGROUND: Interaction between estrogen and estrogen receptor (ER) takes part in the regulation and differentiation of breast tumorigenesis. Some ERα polymorphisms, including ERα rs3798577, are reported to be associated with the risk and aggressiveness of breast carcinoma since the site was reported to be targeted by microRNA, which can further modulate the ERα expression. Hence, this study was conducted to disclose the possible role of ERα SNP rs3798577 on breast carcinoma patients.METHODS: Samples were taken from the post-mastectomy breast carcinoma tissues of female patients and screened based on the completeness of medical and histopathological records. DNA isolation was proceeded using real time-polymerase chain reaction (RT-PCR) then analyzed for high resolution melting (HRM). The nucleotide base sequence was then analyzed based on rs3798577 ERα polymorphism. ER immunohistochemistry test was carried out and counted quantitatively based on the staining intensity and the percentage of the stained cells.RESULTS: Out of 65 samples, there were 33 samples as wild type and 32 samples as variant type. Most variant and wild type had >80% ERα percentage. Most variant type had middle ERα intensity, while wild type had strong ERα intensity. Higher percentage of variant type (52.2%) was found with weak ERα histoscore, meanwhile higher percentage of wild type (52.4%) was found with strong ERα histoscore, but not significant (p=0.725).CONCLUSION: ERα rs3798577 variant type had a lower ERα intensity and weaker ERα histoscore compared to the wild type, suggesting that ERα rs3798577 polymorphism might play a role in breast carcinoma risk determination.KEYWORDS: breast cancer, ERα, rs3798577, polymorphism, immunoexpression
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