Epithelial-to-mesenchymal transition in the development and progression of adenocarcinoma and squamous cell carcinoma of the lung

被引:125
作者
Prudkin, Ludmila
Liu, Diane D. [2 ]
Ozburn, Natalie C. [3 ]
Sun, Menghong
Behrens, Carmen [3 ]
Tang, Ximing [3 ]
Brown, Kathlynn C. [4 ,5 ]
Bekele, B. Nebiyou [2 ]
Moran, Cesar
Wistuba, Ignacio I. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Unit 85, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[4] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Div Translat Res, Dallas, TX 75390 USA
[5] Univ Texas SW Med Ctr Dallas, Simmons Comprehens Canc Ctr, Dallas, TX 75390 USA
关键词
epithelial-to-mesenchymal transition; tissue microarray; immunohistochemical analysis; lung cancer; preneoplasia; brain metastases; GROWTH-FACTOR RECEPTOR; E-CADHERIN EXPRESSION; BETA-CATENIN; CANCER; INVASION; SENSITIVITY; ADHESION; TUMOR; MATRIX-METALLOPROTEINASE-9; METASTASIS;
D O I
10.1038/modpathol.2009.19
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Epithelial-to-mesenchymal transition is a process in which cells undergo a developmental switch from an epithelial to a mesenchymal phenotype. We investigated the role of this phenomenon in the pathogenesis and progression of adenocarcinoma and squamous cell carcinoma of the lung. Archived tissue from primary tumors (n = 325), brain metastases (n = 48) and adjacent bronchial epithelial specimens (n = 192) were analyzed for immunohistochemical expression by image analysis of E-cadherin, N-cadherin, integrin-alpha V beta 6, vimentin, and matrix metalloproteinase-9. The findings were compared with the patients' clinicopathologic features. High expression of the epithelial-to-mesenchymal transition phenotype (low E-cadherin and high N-cadherin, integrin-alpha V beta 6, vimentin, and matrix metalloproteinase-9) was found in most lung tumors examined, and the expression pattern varied according to the tumor histologic type. Low E-cadherin membrane and high N-cadherin cytoplasmic expression were significantly more common in squamous cell carcinoma than in adenocarcinoma (P = 0.002 and 0.005, respectively). Dysplastic lesions had significantly lower expression of the epithelial-to-mesenchymal transition phenotype than the squamous cell carcinomas, and integrin-alpha V beta 6 membrane expression increased stepwise according to the histopathologic severity. Brain metastases had decreased epithelial-to-mesenchymal transition expression compared with primary tumors. Brain metastases had significantly lower integrin-alpha V beta 6 membrane (P = 0.04), N-cadherin membrane, and cytoplasm (P < 0.0002) expression than the primary tumors. The epithelial-to-mesenchymal transition phenotype is commonly expressed in primary squamous cell carcinoma and adenocarcinoma of the lung; this expression occurs early in the pathogenesis of squamous cell carcinoma. Brain metastases showed characteristics of reversed mesenchymal-to-epithelial transition. Our findings suggest that epithelial-to-mesenchymal transition is a potential target for lung cancer chemoprevention and therapy. Modern Pathology (2009) 22, 668-678; doi: 10.1038/modpathol.2009.19; published online 6 March 2009
引用
收藏
页码:668 / 678
页数:11
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