Statistical analysis The statistical significance of the methylation bead chip array data was determined using a paired t test based on B means. The methylated intensity ratio in CRC was confirmed by fold change and odds ratio. The false discovery rate was controlled by adjusting the P value using the Benjamini Hochberg algorithm, the incor rectly substituted probabilities of specifically observed methylation CpG sites for each gene in P values. The methylated intensity ratio of QMSP was determined by the percentage of methylated reference gene, and the PMR value was defined as × 100. The significance of dif ferent PMR values among CRC tissues and adjacent nor mal tissues was defined with the chi squared test and analysis of variance test using Sigma Stat. All statistical tests were two sided and P values of 0.
05 were considered to indicate statistical significance. Results Selection of 21 hypermethylated candidate genes in CRC To identify the aberrant methylation of various genes in CRC, we performed a methylation chip array in 10 normal colon tissues, and 21 CRC tissues and adjacent normal tissues. We found a total of 3,177 {from this source| selleckchem|selleck|selleck|ML323 dissolve solubility CpG sites in the pro moter regions and non promoter regions, with aberrant methylated CpG sites identified in CRC tissues compared with adja cent normal and normal colon tissues, according to statis tical significance determined by the paired t test and an FDR P value of 0. 001 based on a B mean of 0. 1. Among 3,177 CpG sites, we identified 597 genes with hyper methylated CpG sites in promoter CpG islands.
Finally, we selected 21 Mupirocin structure candidate genes that con tained strongly hypermethylated CpG sites in promoter CpG islands in CRC tissues compared with adjacent nor mal tissues. Validation of 39 genes by QMSP To confirm the methylation status of 21 candidate genes from the array results and 18 CIMP markers, we vali dated the methylation status in the promoter CpG islands of selected genes by QMSP in 10 different CRC tissues compared with adjacent normal tissue. The quan titative analysis with the PMR value supported the differ ential methylation status between CRC and normal tissues. The methylation status in the promoter CpG islands of all candidate genes was frequently higher in CRC tissues compared with adjacent normal tissues except FLI.
The methylation status of 12 CIMP markers, namely, ADAMTS1, CHFR, IGF2, IGFBP3, NEU ROG1, SFRP1, WRN, CRABP1, MGMT, RASSF1A, RUNX3, and SFRP2 was also frequently higher in CRC tissues compared with adjacent normal tissues. In normal colon cells, SLC8A3, ZNF272, IGF2, APC, MGMT, and CDKN2A were methylated. All genes were hypermethylated in one or more CRC cell lines except WRN. Demethylation effect of vincristine on 29 hypermethylated genes in CRC cell lines The 10 genes hypermethylated in normal colon cells or not significantly hypermethylated in tumor tissue were excluded for chemical treatment.