Assessment of immunohistochemical expression of claudin-1 in oral squamous cell carcinoma and its clinicopathological correlation

Poonam Rajendra Zanwar, Jayanti Govind Humbe, Jyoti Dilip Bhavthankar, Mandakini Subhash Mandale, Priyanka Sanjay Pachpande
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Abstract

Oral carcinogenesis is complex and multi-step process, which results from various deleterious habits, multiple environmental factors and genetic susceptibility. CLDN-1 expression is regulated oncogenic Wnt/B-catenin transduction pathway. They recruit matrix metalloproteinases (MMPs) on the cell surface to achieve elevated focal concentrations and eventual activations of proMMP2. These collagenases are responsible for the breakdown of extracellular matrix proteins and thus facilitate invasion and spread of malignant cells. Reduced cell-cell adhesion is associated with loss of contact inhibition of proliferation. This allows escape from growth control signals and triggers carcinogenesis. Significant correlation was observed between histopathological grade of the tumor with the localization and immunostaining intensity of CLDN-1. Determination of localization of CLDN-1 for a particular patient may be important to decide site (cytoplasmic or nuclear) for targeting CLDN-1. This targeted drug therapy for CLDN-1 may prevent worsening of the disease in the patient, resulting in better prognosis.
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claudin-1在口腔鳞状细胞癌中的免疫组化表达及临床病理相关性研究
口腔癌变是一个复杂的多步骤过程,是多种不良生活习惯、多种环境因素和遗传易感性共同作用的结果。CLDN-1的表达受Wnt/ b -连环蛋白转导通路的调控。它们在细胞表面募集基质金属蛋白酶(MMPs),以达到升高的病灶浓度并最终激活proMMP2。这些胶原酶负责细胞外基质蛋白的分解,从而促进恶性细胞的侵袭和扩散。细胞-细胞粘附减少与接触丧失、增殖抑制有关。这使得生长控制信号逃逸,并引发癌变。肿瘤的组织病理学分级与CLDN-1的定位及免疫染色强度有显著相关性。确定特定患者CLDN-1的定位对于确定CLDN-1的靶向位置(细胞质或细胞核)可能很重要。这种针对CLDN-1的靶向药物治疗可以防止患者疾病的恶化,从而获得更好的预后。
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