PTEN and α-SMA Expression and Diagnostic Role in Oral Submucous Fibrosis and Oral Squamous Cell Carcinoma with Concomitant Oral Submucous Fibrosis.

IF 1 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
eJournal of Oral Maxillofacial Research Pub Date : 2021-03-31 eCollection Date: 2021-01-01 DOI:10.5037/jomr.2021.12103
Roshni Monteiro, Kaveri Hallikeri, Archana Sudhakaran
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引用次数: 3

Abstract

Objectives: The diagnostic role and correlation between phosphatase and tensin homologue and alpha-smooth muscle actin in oral submucous fibrosis and oral squamous cell carcinoma with concomitant oral submucous fibrosis was analysed by this case control study. The mechanism by which phosphatase and tensin homologue controls myofibroblast expression was also evaluated.

Material and methods: Overall, 10 normal mucosa, 30 oral submucous fibrosis (OSF) and 30 oral squamous cell carcinoma (OSCC) with OSF were stained immunohistochemically with phosphatase and tensin homologue (PTEN) and alpha-smooth muscle actin (α-SMA). Percentage positivity, pattern of expression was statistically compared using Pearson's Chi-square and Fischer exact tests. The correlation between markers was analysed using Spearman correlation.

Results: OSF and OSCC affected males predominantly with majority below 40 years and above 40 years of age respectively. Percentage of PTEN positive cells was statistically significant with gender (P = 0.024) and α-SMA distribution of pattern showed a significant correlation with habits (P = 0.018). A significant decrease in nuclear PTEN positivity (P < 0.001) and a gradual increase in α-SMA cytoplasmic expression was noted from NM to OSF and OSCC. A statistically significant weak inverse correlation existed between PTEN and α-SMA.

Conclusions: A reduced phosphatase and tensin homologue expression in oral submucous fibrosis makes it more prone for malignant transformation. An increase in stromal desmoplasia modifies differentiation, invasive and proliferative capacity of tumour cells. As phosphatase and tensin homologue functions through P-Akt pathway, P-Akt with phosphatase and tensin homologue could be a therapeutic target.

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PTEN和α-SMA在口腔黏膜下纤维化和口腔鳞状细胞癌合并口腔黏膜下纤维化中的表达及诊断作用
目的:通过病例对照研究,分析磷酸酶、紧张素同源物和α -平滑肌肌动蛋白在口腔黏膜下纤维化和口腔鳞状细胞癌合并口腔黏膜下纤维化中的诊断作用及相关性。磷酸酶和紧张素同源物控制肌成纤维细胞表达的机制也被评估。材料和方法:对10例正常黏膜、30例口腔黏膜下纤维化(OSF)和30例口腔鳞癌(OSCC)粘膜进行免疫组化染色,采用磷酸酶和紧张素同源物(PTEN)和α-平滑肌肌动蛋白(α-SMA)进行染色。阳性百分率、表达模式采用Pearson卡方检验和Fischer精确检验进行统计学比较。采用Spearman相关分析标记物之间的相关性。结果:OSF和OSCC以男性为主,分别以40岁以下和40岁以上男性居多。PTEN阳性细胞百分比与性别差异有统计学意义(P = 0.024), α-SMA模式分布与习惯差异有统计学意义(P = 0.018)。从NM到OSF和OSCC,细胞核PTEN阳性显著降低(P < 0.001), α-SMA细胞质表达逐渐升高。PTEN与α-SMA呈显著的负相关。结论:口腔黏膜下纤维化组织中磷酸酶和紧张素同源物表达的减少使其更容易发生恶性转化。间质结缔组织增生的增加改变了肿瘤细胞的分化、侵袭和增殖能力。磷酸酶和紧张素同源物通过P-Akt通路发挥作用,P-Akt与磷酸酶和紧张素同源物可能成为治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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