4.7 Article

Impact of smoking on the expression of claudins in lung carcinoma

Journal

EUROPEAN JOURNAL OF CANCER
Volume 47, Issue 4, Pages 620-630

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.ejca.2010.10.017

Keywords

Smoking; Tight junction; Immunohistochemistry; Epithelial cells

Categories

Funding

  1. Finnish Anti-Tuberculosis Association Foundation the Academy of Finland
  2. Jalmari and Rauha Ahokas Foundation
  3. Finnish Cancer Society
  4. Oulu and Kuopio University Hospital

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Rationale: Tight junctions regulate the paracellular permeability and orientation of cells and claudins are key components of tight junctions. Objectives: To study the influence of cigarette smoke on claudin expression in vitro and in lung cancer patients. Methods: We studied the effect of smoking on claudin expression by exposing a bronchial cell line (BEAS-2B) and two carcinoma cell lines (SK-LU1 and SK-MES1) to tobacco smoke for 48 h and analysed their claudin mRNA expression. The relation between smoked pack years and protein expression of claudins 1-5 and 7 in 344 lung cancer patients was determined by immunohistochemistry. Measurements and main results: In BEAS-2B cells and SK-LU1 cells, an initial increase was followed by a decline in the mRNA expression of several claudins. In SK-MES1 cells, no evident elevation in claudin expression was observed. Intense claudin 1 and 4 positivity was found more often in cancer samples of smokers and ex-smokers compared to non-smokers (p < 0.001 and p = 0.003, respectively). Heavy smokers with longer than 40 pack-years consumption had more often intense claudin 1 (p = 0.011), 4 (p = 0.050) or 7 (p = 0.058) expression in squamous cell carcinoma compared to non-smokers or smokers with fewer pack-years. Claudin 1 positivity predicted a better survival in adenocarcinoma (p = 0.044) and in squamous cell carcinoma (p = 0.027) and claudin 4 positivity in adenocarcinoma only (p = 0.048). In squamous cell carcinoma, claudin 7 positivity was associated with a better survival (p = 0.011). Conclusions: Bronchial BEAS-2B cells and SK-LU1 cells respond to tobacco smoke by changing their claudin mRNA synthesis and resulting tight junction permeability changes may thus contribute to tobacco induced carcinogenesis both during initiation and progression. This concept is strengthened by findings in the clinical tumour material, where tobacco consumption was associated with claudin expression. (c) 2010 Elsevier Ltd. All rights reserved.

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