乳腺癌患者肿瘤分级对 Ezrin 和 Radixin 的上调作用

Hadiseh Mohammad pour, Reza Shirkoohi
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引用次数: 0

摘要

背景乳腺癌(BC)是伊朗妇女死亡的主要原因之一。参与疾病促进和进展的生物标志物对于管理和控制乳腺癌的结果非常重要。在这项研究中,我们旨在估测 BC 患者体内 Ezrin 和 Radixin 的表达水平及其与病理因素的关系。Ezrin 和 Radixin 是细胞形态发生、内吞、外吞、粘附和迁移过程中的两个重要因子。研究方法113 名 BC 患者参与了这项研究。采用实时定量 PCR 技术估算 Ezrin 和 Radixin 基因的相对表达量。根据病理报告记录患者的组织学、肿瘤大小、分级、淋巴管侵犯和临床 TNM(肿瘤、结节和转移)分期等病理数据,并估计其与 Ezrin 和 Radixin 基因相对表达的关系。结果结果显示,与邻近的正常组织相比,Ezrin在肿瘤样本中表达过高。Ezrin和Radixin的过度表达与肿瘤的分级和坏死有明显关系。此外,Ezrin 的相对表达与 Radixin 的表达也有直接关系。结论:这些数据支持 Ezrin 和 Radixin 在乳腺癌生物学中的作用,还需要更多的研究来确定与表型相关的 Ezrin 和 Radixin,并将其验证为癌症进展的标志物和癌症治疗的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Up Regulation of Ezrin and Radixin with respect to Grade of Tumors in Breast Cancer Patients
Background: Breast cancer (BC) is one of the main causes of death among women in Iran. Biomarkers involved in promotion and progression of disease is very important in management and control of BC outcomes. In this research, we aim to estimate the expression levels of Ezrin and Radixin, as two important factors in morphogenesis, endocytosis, exocytosis, adherence, and migration of cells, in BC patients and their relationship with pathological factors. Methods: One hundred and thirteen BC patients were involved in this research. Relative expression of Ezrin and Radixin genes were estimated with quantitative real-time PCR. Pathological data include the histology, tumor size, grade, lymphovascular invasion and clinical TNM (Tumor, Node, and Metastasis) staging of patients were recorded based on the pathology report and their relationship with relative expression of Ezrin and Radixin were estimated. Result: According to result Ezrin were over expressed in tumor samples in comparison to adjacent normal tissue. There is a significant relationship between over expression of Ezrin and Radixin and grade of tumor and necrosis. Also there is a direct relationship between relative expression of Ezrin and Radixin expression. Conclusions: These data support the role of Ezrin and Radixin in the biology of breast cancer and additional studies needed that determine the Ezrin and Radixin associated with phenotype and may validate them as markers of cancer progression and as a potential target for cancer therapy.
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