Altered expression of junctional proteins as a potential biomarker in oral precancerous and cancerous patients.

IF 3.6 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Tissue Barriers Pub Date : 2022-04-03 Epub Date: 2021-09-17 DOI:10.1080/21688370.2021.1973329
Puja Upadhaya, Sarbani Giri, Dharmeswar Barhoi, Abhinandan Bhattacharjee
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引用次数: 1

Abstract

Due to a lower survival rate in patients with advanced clinical stages of oral cancer, discovering a biomarker that could diagnose and predict disease progression is vital. Cell-cell junctional proteins play a crucial role in the maintenance of tissue architecture but are often deregulated in different cancer. The present study investigates the expression of cell-cell junctional proteins viz: e-cadherin (E-cad) and zonula occludens-1 (ZO-1) in oral precancerous (OED) and cancerous (OSCC) patients to monitor if they can serve as practicable molecular markers. The ultrastructural junctional complex was studied by transmission electron microscopy, and the expression of proteins was performed by immunohistochemistry. The relationship between the expression of protein and clinicopathological features of the patients was checked by Pearson's correlation test. Furthermore, the survival curve of the follow-up data was estimated by the Kaplan-Meier method. We observed a disrupted junctional complex and a significantly decreased immunoexpression of E-cad and ZO-1 in OED and OSCC when compared to the adjacent non-cancerous tissues. The expression of ZO-1 was associated with TNM stages, whereas E-cad was associated with histological grades as well as TNM stages. A positive correlation was observed between the expression of ZO-1 and E-cad proteins in OED and OSCC. Further, follow-up studies revealed that high ZO-1 and E-cad expressing patients survived longer than their low expressed counterparts. The present study shows disruption of junctional complex and alteration of junctional proteins expression that could draw the attention of health professionals to explore junctional proteins as a possible therapeutic target in oral cancer.

Abstract Image

Abstract Image

口腔癌前和癌前患者中连接蛋白表达改变作为潜在生物标志物。
由于口腔癌晚期患者的生存率较低,发现一种能够诊断和预测疾病进展的生物标志物至关重要。细胞-细胞连接蛋白在组织结构的维持中起着至关重要的作用,但在不同的癌症中往往不受调节。本研究研究了细胞-细胞连接蛋白,即e-钙粘蛋白(E-cad)和小带闭塞-1 (ZO-1)在口腔癌前(OED)和癌前(OSCC)患者中的表达,以监测它们是否可以作为可行的分子标志物。透射电镜观察连接复合物超微结构,免疫组织化学检测蛋白表达。采用Pearson相关检验检测蛋白表达与患者临床病理特征的关系。采用Kaplan-Meier法估计随访资料的生存曲线。我们观察到,与邻近的非癌组织相比,OED和OSCC中的连接复合物被破坏,E-cad和ZO-1的免疫表达显著降低。ZO-1的表达与TNM分期有关,而E-cad与组织学分级和TNM分期有关。ZO-1和E-cad蛋白在OED和OSCC中的表达呈正相关。此外,随访研究显示,高ZO-1和E-cad表达的患者比低表达的患者存活时间更长。目前的研究表明,连接复合体的破坏和连接蛋白表达的改变可能引起卫生专业人员的注意,以探索连接蛋白作为口腔癌可能的治疗靶点。
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来源期刊
Tissue Barriers
Tissue Barriers MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
6.60
自引率
6.50%
发文量
25
期刊介绍: Tissue Barriers is the first international interdisciplinary journal that focuses on the architecture, biological roles and regulation of tissue barriers and intercellular junctions. We publish high quality peer-reviewed articles that cover a wide range of topics including structure and functions of the diverse and complex tissue barriers that occur across tissue and cell types, including the molecular composition and dynamics of polarized cell junctions and cell-cell interactions during normal homeostasis, injury and disease state. Tissue barrier formation in regenerative medicine and restoration of tissue and organ function is also of interest. Tissue Barriers publishes several categories of articles including: Original Research Papers, Short Communications, Technical Papers, Reviews, Perspectives and Commentaries, Hypothesis and Meeting Reports. Reviews and Perspectives/Commentaries will typically be invited. We also anticipate to publish special issues that are devoted to rapidly developing or controversial areas of research. Suggestions for topics are welcome. Tissue Barriers objectives: Promote interdisciplinary awareness and collaboration between researchers working with epithelial, epidermal and endothelial barriers and to build a broad and cohesive worldwide community of scientists interesting in this exciting field. Comprehend the enormous complexity of tissue barriers and map cross-talks and interactions between their different cellular and non-cellular components. Highlight the roles of tissue barrier dysfunctions in human diseases. Promote understanding and strategies for restoration of tissue barrier formation and function in regenerative medicine. Accelerate a search for pharmacological enhancers of tissue barriers as potential therapeutic agents. Understand and optimize drug delivery across epithelial and endothelial barriers.
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