Ac1PathwayRALBP1 TRIO CDK5 MYLK PIK3R1 WASF1 MAP3K1 PAK

Ac1PathwayRALBP1 TRIO CDK5 MYLK PIK3R1 WASF1 MAP3K1 PAK1 RAC1 CFL1 ARFIP2 LIMKa Derived from logistic regression model with adjustment for age, gender, pack-year of smoking and principal components in combined dataset of Nanjing and Beijing studies. doi:10.1371/journal.pone.0057763.tnew insights into the biology of a certain disease utilizing GWAS data. GSEA has two major advantages compared with other methods [16,26]. First, it performs two-step permutation-based correction procedure which effectively adjusts for different sizes of genes and preserves correlations of SNPs in the same gene. Second, covariates such as age, gender or population stratificationin GWAS can be adjusted in GSEA. Thus, in the current study, we used GSEA and identified four pathways (achPathway, 23977191 metPathway, At1rPathway and rac1Pathway) that may play an important role in the development of lung cancer in Han Chinese population. These findings were stable after sensitivity analysisPathway Analysis for GWAS of Lung Cancerwhen considering the SNP-to-gene mapping approach and gene overlapping between pathways. The achPathway (Role of nicotinic acetylcholine receptors in the regulation of apoptosis) was identified to be the top pathways associated with lung cancer risk in this study. Nicotinic acetylcholine receptors (nAchRs) are essential for neuromuscular signaling and have also been found on non-neuronal cells, such as MedChemExpress JSI124 bronchial epithelial cells and lung cancer cell lines [32,33,34]. Nicotine and its derived carcinogenic nitrosamines may play an important role in the pathogenesis of lung cancer through the binding to nAChRs expressed in lung epithelial cells, which mainly result from the resistance of cancer cells to apoptosis [35]. Maneckjee et al. (1994) showed that low concentrations of nicotine could block the induction of apoptosis in lung cancer cells [33]. In addition to conferring resistance against apoptosis, several studies have shown that nAChRs can induce cell proliferation as well as angiogenesis [36,37], both of which are involved in the genesis of cancer. Importantly, several GWAS based on Caucasian populations have consistently identified 15q25 as lung cancer susceptibility region [5,6,7], which contains the nicotinic acetylcholine receptor subunit gene cluster, harboring CHRNA5, CHRNA3 and CHRNA4 genes. TERT is included in the achPathway and its representative SNP rs2736100 has been identified as a lung cancer susceptibility locus in different ethnic populations [3,8], especially in Asian populations [38,39,40]. In the At1rPathway (Angiotensin II mediated activation of JNK Pathway via Pyk2 dependent signaling), Clereet. al (2010) proposed that angiotensin II Type 2 receptor (AT2R) would promote tumor development, including both malignant cell proliferation and tumor angiogenesis [41]. Over-expression of angiotensin II type 2 receptor gene induces cell death in lung adenocarcinoma cells [42,43]. The aberrant activated JNK pathway can cause pathological cell death and different diseases including cancer [44], while get SIS3 mutations in the JNK pathway can also be involved in cancer development [45]. For the metPathway (Signaling of Hepatocyte Growth Factor Receptor), the hepatocyte growth factor receptor, also called cMet, is activated by hepatocyte growth factor (HGF). Aberrant cMet signaling plays significant roles in the pathogenesis and biology of human cancers [46]. Meanwhile, Mutated and overexpressed forms of c-Met are associated with oncogenesis and.Ac1PathwayRALBP1 TRIO CDK5 MYLK PIK3R1 WASF1 MAP3K1 PAK1 RAC1 CFL1 ARFIP2 LIMKa Derived from logistic regression model with adjustment for age, gender, pack-year of smoking and principal components in combined dataset of Nanjing and Beijing studies. doi:10.1371/journal.pone.0057763.tnew insights into the biology of a certain disease utilizing GWAS data. GSEA has two major advantages compared with other methods [16,26]. First, it performs two-step permutation-based correction procedure which effectively adjusts for different sizes of genes and preserves correlations of SNPs in the same gene. Second, covariates such as age, gender or population stratificationin GWAS can be adjusted in GSEA. Thus, in the current study, we used GSEA and identified four pathways (achPathway, 23977191 metPathway, At1rPathway and rac1Pathway) that may play an important role in the development of lung cancer in Han Chinese population. These findings were stable after sensitivity analysisPathway Analysis for GWAS of Lung Cancerwhen considering the SNP-to-gene mapping approach and gene overlapping between pathways. The achPathway (Role of nicotinic acetylcholine receptors in the regulation of apoptosis) was identified to be the top pathways associated with lung cancer risk in this study. Nicotinic acetylcholine receptors (nAchRs) are essential for neuromuscular signaling and have also been found on non-neuronal cells, such as bronchial epithelial cells and lung cancer cell lines [32,33,34]. Nicotine and its derived carcinogenic nitrosamines may play an important role in the pathogenesis of lung cancer through the binding to nAChRs expressed in lung epithelial cells, which mainly result from the resistance of cancer cells to apoptosis [35]. Maneckjee et al. (1994) showed that low concentrations of nicotine could block the induction of apoptosis in lung cancer cells [33]. In addition to conferring resistance against apoptosis, several studies have shown that nAChRs can induce cell proliferation as well as angiogenesis [36,37], both of which are involved in the genesis of cancer. Importantly, several GWAS based on Caucasian populations have consistently identified 15q25 as lung cancer susceptibility region [5,6,7], which contains the nicotinic acetylcholine receptor subunit gene cluster, harboring CHRNA5, CHRNA3 and CHRNA4 genes. TERT is included in the achPathway and its representative SNP rs2736100 has been identified as a lung cancer susceptibility locus in different ethnic populations [3,8], especially in Asian populations [38,39,40]. In the At1rPathway (Angiotensin II mediated activation of JNK Pathway via Pyk2 dependent signaling), Clereet. al (2010) proposed that angiotensin II Type 2 receptor (AT2R) would promote tumor development, including both malignant cell proliferation and tumor angiogenesis [41]. Over-expression of angiotensin II type 2 receptor gene induces cell death in lung adenocarcinoma cells [42,43]. The aberrant activated JNK pathway can cause pathological cell death and different diseases including cancer [44], while mutations in the JNK pathway can also be involved in cancer development [45]. For the metPathway (Signaling of Hepatocyte Growth Factor Receptor), the hepatocyte growth factor receptor, also called cMet, is activated by hepatocyte growth factor (HGF). Aberrant cMet signaling plays significant roles in the pathogenesis and biology of human cancers [46]. Meanwhile, Mutated and overexpressed forms of c-Met are associated with oncogenesis and.