乳腺丝氨酸蛋白酶抑制剂(MASPIN)在局部进展期口腔鳞状细胞癌中的亚细胞表达

S. Zaheer, A. Nagi
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引用次数: 1

摘要

目的:乳腺丝氨酸蛋白酶抑制剂(MASPIN)与肿瘤的发病和进展有许多相互作用。其与细胞凋亡和血管生成的关系已被证实对预后有影响。然而,它的确切作用尚不清楚,需要进一步研究与各种人类癌症的关系。本研究拟探讨MASPIN在口腔鳞状细胞癌(OSCC)中的亚细胞表达,并观察其与肿瘤分级的关系。方法:这是一项描述性研究,在拉合尔卫生科学大学病态解剖与组织病理学系进行。50例确诊为鳞状细胞癌,采用免疫组化染色亲和生物素-过氧化物酶复合物法检测MASPIN的表达。根据染色强度和阳性细胞百分比对MASPIN表达进行评分。采用SPSS统计软件对数据进行分析。结果:患者平均年龄56.84 ±1.58岁,男女比例为1.3:1。所有肿瘤均局部进展(III期)。组织学上,58%的肿瘤为1级,其他级别较少见。32例(64%)患者表达MASPIN,且均定位于肿瘤细胞的细胞质中。阳性15例(44.1%)表现为局灶性,13例(38.2%)表现为弥漫但中度,6例(17.7%)表现为弥漫而强烈。MASPIN表达与肿瘤分级呈显著相关(P: 0.043),与肿瘤分级呈负相关(P: 0.034)。结论:在大多数OSCC中可见MASPIN的表达。然而,在所有病例中,它都定位于肿瘤细胞的细胞质。在低分化癌症中,MASPIN的表达缺失更为常见。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subcellular Expression of Mammary Serine Proteinase Inhibitor (MASPIN) in Locally Advance Oral Squamous Cell Carcinoma
Objectives: Mammary serine protease inhibitor (MASPIN) has numerous interactions with tumor pathogenesis and progression. Its relationships with apoptosis and angiogenesis have proven the impact on prognosis. However, its exact role is not known and needs further work in relation to various human cancers. Current study was planned to investigate the subcellular expression of MASPIN in oral squamous cell carcinoma (OSCC) and to observe its relation with tumor grade. Methods: It was a descriptive study, conducted at the Department of Morbid Anatomy and Histopathology, University of Health Sciences, Lahore. Histological diagnosis of squamous cell carcinoma was confirmed in 50 cases, and expression of MASPIN was determined by avidinbiotin-peroxidase complex method of immunohistochemical staining. MASPIN expression was scored on the basis of intensity of staining and the percentage of the cells that stained positively. Data was analyzed with SPSS using appropriate statistical procedures. Results: Mean age of the patients was 56.84 ± 1.58 years with male to female ratio 1.3:1. All tumors were locally advancing (Stage III). Histologically, 58% tumors were Grade 1, other grades were less common. MASPIN expression was observed in 32 (64%) cases, and it was localized to the cytoplasm of the tumor cells in all cases. Among the positive cases, its expression was focal in 15 (44.1%), diffuse but moderate in 13 (38.2%) and diffuse and intense in 6(17.7%) cases. MASPIN expression was significantly associated (P: 0.043) and negatively correlated (P: 0.034) with tumor grade. Conclusions: MASPIN expression was observed in the majority of OSCC. However, it was localized to the cytoplasm of tumor cells in all cases. Loss of MASPIN expression was observed more frequently in poorly differentiated cancers.
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