Evaluation of the Ultrastructure and Expression of Desmoglein 2 in Breast Cancer: A Novel Biomarker

Pub Date : 2021-05-24 DOI:10.21203/RS.3.RS-506346/V1
Maryam Mohammadhosseini, H. Mirzaei, A. Majd, M. Farhadi, N. Shayanfar
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Abstract

BackgroundBreast cancer is the most common malignancy among Iranian women. In recent years, the study of dysfunction in the expression of cell-cell junction genes and the related proteins in the malignant process has been at the center of attention. MethodsIn this study, 50 patients were selected who had both cancerous tissue and adjacent healthy tissue. The expression of the desmoglein 2 gene was evaluated. Healthy and cancerous tissue were compared using routine hematoxylin and eosin staining. The total protein was also compared between these two groups. The ultrastructural examination was performed.ResultsThe real-time polymerase chain reaction results showed a decrease in the expression of the desmoglein 2 gene in all tumor samples compared to the healthy samples (p-value <0.0001). Besides, receiver operating characteristic curve analysis showed that the area under the curve was equal to 0.98. Transmission electron microscopy microscopic studies revealed a change in the status of desmosomal junctions. These findings were consistent with the qualitative decrease in the protein expression between the two target groups.ConclusionOverall, the findings showed that the association between desmoglein 2 gene expression and alterations in cellular connections leads to impaired cellular connections, which is an important risk factor for breast cancer. This result proposed the understudy gene as a new biomarker in the development of breast cancer.
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一种新的生物标志物:乳腺癌中纤粒蛋白2的超微结构和表达的评价
背景:乳腺癌是伊朗妇女中最常见的恶性肿瘤。近年来,对恶性肿瘤过程中细胞-细胞连接基因及相关蛋白表达功能障碍的研究一直是人们关注的焦点。方法本研究选择50例既有癌组织又有邻近健康组织的患者。测定促粘蛋白2基因的表达。用常规苏木精和伊红染色对健康组织和癌变组织进行比较。并比较两组总蛋白含量。进行超微结构检查。结果实时聚合酶链反应结果显示,所有肿瘤标本中desmoglin 2基因的表达均低于健康标本(p值<0.0001)。此外,受试者工作特征曲线分析显示,曲线下面积为0.98。透射电子显微镜下的研究显示了桥粒连接状态的改变。这些发现与两个靶组之间蛋白表达的定性下降一致。结论综上所述,桥蛋白2基因表达与细胞连接改变相关,可导致细胞连接受损,这是乳腺癌的重要危险因素。这一结果表明,understudy基因可能是乳腺癌发展过程中的一个新的生物标志物。
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