Paul Sunirmal, Amundson Sally A
Center for Radiological Research, Columbia University Medical Center, New York, NY ; Department of Radiology, New Jersey Medical School, Cancer Center RUTGERS, Newark, NJ.
Center for Radiological Research, Columbia University Medical Center, New York, NY.
J Carcinog Mutagen. 2014;5. doi: 10.4172/2157-2518.1000198.
Smoking is the second leading cause of preventable death in the United States. Cohort epidemiological studies have demonstrated that women are more vulnerable to cigarette-smoking induced diseases than their male counterparts, however, the molecular basis of these differences has remained unknown. In this study, we explored if there were differences in the gene expression patterns between male and female smokers, and how these patterns might reflect different sex-specific responses to the stress of smoking. Using whole genome microarray gene expression profiling, we found that a substantial number of oxidant related genes were expressed in both male and female smokers, however, smoking-responsive genes did indeed differ greatly between male and female smokers. Gene set enrichment analysis (GSEA) against reference oncogenic signature gene sets identified a large number of oncogenic pathway gene-sets that were significantly altered in female smokers compared to male smokers. In addition, functional annotation with Ingenuity Pathway Analysis (IPA) identified smoking-correlated genes associated with biological functions in male and female smokers that are directly relevant to well-known smoking related pathologies. However, these relevant biological functions were strikingly overrepresented in female smokers compared to male smokers. IPA network analysis with the functional categories of immune and inflammatory response gene products suggested potential interactions between smoking response and female hormones. Our results demonstrate a striking dichotomy between male and female gene expression responses to smoking. This is the first genome-wide expression study to compare the sex-specific impacts of smoking at a molecular level and suggests a novel potential connection between sex hormone signaling and smoking-induced diseases in female smokers.
吸烟是美国可预防死亡的第二大主要原因。队列流行病学研究表明,女性比男性更容易患吸烟诱发的疾病,然而,这些差异的分子基础仍然未知。在本研究中,我们探讨了男性和女性吸烟者之间基因表达模式是否存在差异,以及这些模式如何反映对吸烟压力的不同性别特异性反应。通过全基因组微阵列基因表达谱分析,我们发现大量与氧化剂相关的基因在男性和女性吸烟者中均有表达,然而,吸烟反应性基因在男性和女性吸烟者之间确实存在很大差异。针对参考致癌特征基因集的基因集富集分析(GSEA)确定,与男性吸烟者相比,女性吸烟者中有大量致癌途径基因集发生了显著改变。此外, Ingenuity途径分析(IPA)的功能注释确定了与男性和女性吸烟者生物学功能相关的吸烟相关基因,这些功能与众所周知的吸烟相关病理直接相关。然而相比男性吸烟者,这些相关生物学功能在女性吸烟者中显著富集。对免疫和炎症反应基因产物功能类别的IPA网络分析表明吸烟反应与女性激素之间可能存在相互作用。我们的结果表明男性和女性对吸烟的基因表达反应存在显著差异。这是第一项在分子水平上比较吸烟对不同性别的影响的全基因组表达研究,并提示女性吸烟者中激素信号与吸烟诱发疾病之间可能存在新的潜在联系。