4.6 Article

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

期刊

MODERN PATHOLOGY
卷 22, 期 5, 页码 668-678

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/modpathol.2009.19

关键词

epithelial-to-mesenchymal transition; tissue microarray; immunohistochemical analysis; lung cancer; preneoplasia; brain metastases

资金

  1. Specialized Program of Research Excellence (SPORE) in Lung Cancer [P50 CA70907, 1RO1CA106646]
  2. National Cancer Institute, Bethesda
  3. Department of Defense [W81XWH-04-1-0142]

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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

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