Downexpression of Matriptase-2 Correlates With Tumor Progression and Clinical Prognosis in Oral Squamous-Cell Carcinoma

被引:5
|
作者
Cheng, Ming-Fang [1 ,3 ,6 ]
Lin, Li-Han [1 ]
Huang, Mao-Suan [5 ]
Lee, Herng-Sheng [7 ]
Ji, Dar-Der [2 ]
Lin, Chun-Shu [4 ]
Hsia, Kan-Tai [1 ]
机构
[1] Natl Yang Ming Univ, Sch Dent, Inst Oral Biol, 155,Sec 2,Li Nong St, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Dept Trop Med, Taipei, Taiwan
[3] Triserv Gen Hosp, Natl Def Med Ctr, Dept Pathol, Taipei, Taiwan
[4] Triserv Gen Hosp, Natl Def Med Ctr, Dept Radiat Oncol, Taipei, Taiwan
[5] Taipei Med Univ, Shuang Ho Hosp, Dept Dent, Taipei, Taiwan
[6] Hualien Armed Forced Gen Hosp, Div Histol & Clin Pathol, Hualien, Taiwan
[7] Kaohsiung Vet Gen Hosp, Dept Pathol & Lab Med, Kaohsiung, Taiwan
关键词
matriptase-2; oral squamous-cell carcinoma; immunohistochemistry; BREAST-CANCER; IN-VITRO; IRON-DEFICIENCY; EXPRESSION; TMPRSS6; GENE; IDENTIFICATION; NEOPLASIA; PROTEASES; GROWTH;
D O I
10.1097/PAI.0000000000000324
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The aim of this study was to investigate the relationship of matriptase-2 expression with the clinicopathologic characteristics, the histologic grade, and patient survival in oral squamous-cell carcinoma (OSCC). Immunohistochemical analysis of matriptase-2 expression was performed in 102 surgical specimens from patients with OSCC. The immunohistochemical results were further verified by quantitative real-time reverse transcription-polymerase chain reaction. The immunostaining intensity was scored on a scale ranging from 0 (absence of staining) to 3 (intense staining). The distribution score was determined by the percentage of stained cells on a scale ranging from 0 (<5%), 1 (5% to 25%), 2 (25% to 50%), 3 (50% to 75%), to 4 (75% to 100%). The immunoscore of matriptase-2 expression was the product of the above 2 scores and ranged from 0 to 12 for analysis. Faint matriptase-2 immunostaining was observed in the non-neoplastic oral mucosal epithelia. The matriptase-2 immunoscore was significantly higher in well-differentiated OSCCs than in poorly differentiated tumors (P=0.001). Moreover, a reduced matriptase-2 immunoscore was inversely correlated with the tumor size (P=0.017), a positive nodal stage (P=0.008), distant metastasis (P=0.032), and a late clinical stage (P=0.001). A lower immunoscore of matriptase-2 expression revealed a significant association with poor survival (P=0.003). Our results demonstrate that the inverse expression of matriptase-2 correlates with tumor progression and an advanced TNM stage, and has a poor prognosis in patients with OSCC. These findings suggest that the expression of matriptase-2 may be both a prognostic marker and a potential therapeutic target for this cancer.
引用
收藏
页码:481 / 488
页数:8
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