Abstract

Cigarette smoke is well known for its adverse effects on human health, especially on the lungs. Basic research is essential to identify the mechanisms involved in the development of cigarette smoke-related diseases, but translation of new findings from pre-clinical models to the clinic remains difficult. In the present study, we aimed at comparing the gene expression signature between the lungs of human smokers and mice exposed to cigarette smoke to identify the similarities and differences. Using human and mouse whole-genome gene expression arrays, changes in gene expression, signaling pathways and biological functions were assessed. We found that genes significantly modulated by cigarette smoke in humans were enriched for genes modulated by cigarette smoke in mice, suggesting a similar response of both species. Sixteen smoking-induced genes were in common between humans and mice including six newly reported to be modulated by cigarette smoke. In addition, we identified a new conserved pulmonary response to cigarette smoke in the induction of phospholipid metabolism/degradation pathways. Finally, the majority of biological functions modulated by cigarette smoke in humans were also affected in mice. Altogether, the present study provides information on similarities and differences in lung gene expression response to cigarette smoke that exist between human and mouse. Our results foster the idea that animal models should be used to study the involvement of pathways rather than single genes in human diseases.

Highlights

  • There are more than one billion cigarette smokers on the planet; cigarette smoking being responsible for five million deaths every year worldwide [1]

  • Similarities in the Number of Genes, Pathways and Biological Functions Affected by Cigarette Smoke in Humans and Mice

  • We initiated the analysis by identifying the number of genes in common on both gene expression microarray platforms used in this study

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Summary

Introduction

There are more than one billion cigarette smokers on the planet; cigarette smoking being responsible for five million deaths every year worldwide [1]. The chronic and insidious nature of smoking-related diseases can reduce the quality of life for many decades. In an effort to limit the social and economic impact of cigarette smoke on our society, it is critical to dissect and decipher the mechanisms by which cigarette smoke impacts lung biology and leads to pulmonary and systemic diseases. Our understanding of the cellular and molecular consequences of cigarette smoke exposure on the lung has expanded tremendously owing to new research tools, and increased availability of clinical samples and animal models. We are still facing the translational challenge associated with the use of animals to model human diseases, including chronic obstructive pulmonary disease (COPD) [2]

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