Form the boundary of cancerous tissue, and pathological examination of this tissue showed no sign of malignant cells.The stage of cancer was classified following the 7th edition of AJCC Cancer Staging Handbook [21]. b Among all 305 cases, five cases lacked histopathological data. doi:10.1371/journal.pone.0067577.Title Loaded From File tGenotyping the Promoter Genetic Variants of the CASP8 GeneGenomic DNA was extracted from cancerous tissues of CRC patients and blood samples of healthy controls by using standard phenol/chloroform method. We followed the same approach and condition described in our previous study to genotype the three genetic variants in the CASP8 promoter region [20]. In brief, the 6 bp/del and 8 bp/del polymorphisms were determined by polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis (PAGE). SNP rs3769821 was genotyped by PCR-RFLP assay.Quantitative RT CR for CASP8 mRNA MedChemExpress 125-65-5 ExpressionTotal RNA was isolated from paired cancerous and paracancerous normal tissues of 99 CRC patients who received no radiotherapy and/or chemotherapy treatment before the surgery by using TRIZOL (Invitrogen, Carlsbad, CA) according toCASP8 Polymorphisms May Not Associated with CRCTable 2. Allele frequencies of rs3834129, rs3769821 and rs113686495 in Han Chinese patients with and without colorectal cancer.SampleNrs3834129 6 bp, n ( ) del, n ( ) 129 (21.15) 145 (21.20) 346 (18.85) 420 (23.60)P*rs3769821 T, n ( ) C, n ( ) 174 (28.72) 183 (26.75) ??P*rs113686495 del, n ( ) 8 bp, n ( ) 164 (26.89) 174 (25.44) ??P*Casea Controlb Casec Controlca305 342 918481 (78.85) 539 (78.80) 1,490 (81.15) 1,360 (76.40)0.436 (71.48) 501 (73.25)0.446 (73.11) 510 (74.56)0.???????One patient failed to be genotyped and was excluded. Including 133 control samples that were reported in Xiao et al. [20]. c Cases and controls were taken from Sun et al. [14]. *Two-sided Chi-square test with Yate’s correction. doi:10.1371/journal.pone.0067577.tbmanufacturer’s instruction. One microgram of total RNA was used to synthesize single-strand cDNA using an oligo (dT) 18-mer as primer and MMLV Reverse Transcriptase (Promega, Madison, WI) in a final reaction volume of 25 mL. Primers CASP8-F (59GCAGAGGGAACCTGGTACAT-39) and CASP8-R (59TCATCCTTGTTGCTTACTTCATAG-39) were used to detect CASP8 mRNA transcripts A (GenBank accession number NM_001228.4), B (NM_033355.3), C (NM_033356.3), F (NM_001080124.1) and G (NM_001080125.1). Real-time PCR was performed on the IQ2 Real-Time PCR system (Bio-Rad, Hercules, CA) with 23727046 the SYBR Premix Ex Taq II (Tli RNaseH Plus; TaKaRa, Otsu, Shiga) and the following amplification condition: an initial denaturation at 94uC for 3 min, followed by 35 cycles of 94uC for 15 s, 50uC for 15 s, and 72uC for 20 s, and a final extension cycle at 72uC for 5 min. The GAPDH (Glyceraldehyde 3-phosphate dehydrogenase) gene was amplified for normalization. We used primer pair 59- CAACTACATGGTTTACATGTTC -39/59-GCCAGTGGACTCCACGAC-39 and same thermal cycling parameters (except for a change of annealing temperature to 55uC) as that of the CASP8 gene to amplify the GAPDH gene. Each sample was performed in two duplicates.Statistical AnalysisStatistical analysis was 23977191 performed using the R program (Version 2.11.1, Vienna, Austria) and a P value less than 0.05 was considered as statistically significant. Power calculations were performed by using the Quanto software [22]. Deviation from the Hardy einberg equilibrium (HWE) was assessed for each variant by using the x2-test (df = 1). Allele fre.Form the boundary of cancerous tissue, and pathological examination of this tissue showed no sign of malignant cells.The stage of cancer was classified following the 7th edition of AJCC Cancer Staging Handbook [21]. b Among all 305 cases, five cases lacked histopathological data. doi:10.1371/journal.pone.0067577.tGenotyping the Promoter Genetic Variants of the CASP8 GeneGenomic DNA was extracted from cancerous tissues of CRC patients and blood samples of healthy controls by using standard phenol/chloroform method. We followed the same approach and condition described in our previous study to genotype the three genetic variants in the CASP8 promoter region [20]. In brief, the 6 bp/del and 8 bp/del polymorphisms were determined by polymerase chain reaction (PCR) and polyacrylamide gel electrophoresis (PAGE). SNP rs3769821 was genotyped by PCR-RFLP assay.Quantitative RT CR for CASP8 mRNA ExpressionTotal RNA was isolated from paired cancerous and paracancerous normal tissues of 99 CRC patients who received no radiotherapy and/or chemotherapy treatment before the surgery by using TRIZOL (Invitrogen, Carlsbad, CA) according toCASP8 Polymorphisms May Not Associated with CRCTable 2. Allele frequencies of rs3834129, rs3769821 and rs113686495 in Han Chinese patients with and without colorectal cancer.SampleNrs3834129 6 bp, n ( ) del, n ( ) 129 (21.15) 145 (21.20) 346 (18.85) 420 (23.60)P*rs3769821 T, n ( ) C, n ( ) 174 (28.72) 183 (26.75) ??P*rs113686495 del, n ( ) 8 bp, n ( ) 164 (26.89) 174 (25.44) ??P*Casea Controlb Casec Controlca305 342 918481 (78.85) 539 (78.80) 1,490 (81.15) 1,360 (76.40)0.436 (71.48) 501 (73.25)0.446 (73.11) 510 (74.56)0.???????One patient failed to be genotyped and was excluded. Including 133 control samples that were reported in Xiao et al. [20]. c Cases and controls were taken from Sun et al. [14]. *Two-sided Chi-square test with Yate’s correction. doi:10.1371/journal.pone.0067577.tbmanufacturer’s instruction. One microgram of total RNA was used to synthesize single-strand cDNA using an oligo (dT) 18-mer as primer and MMLV Reverse Transcriptase (Promega, Madison, WI) in a final reaction volume of 25 mL. Primers CASP8-F (59GCAGAGGGAACCTGGTACAT-39) and CASP8-R (59TCATCCTTGTTGCTTACTTCATAG-39) were used to detect CASP8 mRNA transcripts A (GenBank accession number NM_001228.4), B (NM_033355.3), C (NM_033356.3), F (NM_001080124.1) and G (NM_001080125.1). Real-time PCR was performed on the IQ2 Real-Time PCR system (Bio-Rad, Hercules, CA) with 23727046 the SYBR Premix Ex Taq II (Tli RNaseH Plus; TaKaRa, Otsu, Shiga) and the following amplification condition: an initial denaturation at 94uC for 3 min, followed by 35 cycles of 94uC for 15 s, 50uC for 15 s, and 72uC for 20 s, and a final extension cycle at 72uC for 5 min. The GAPDH (Glyceraldehyde 3-phosphate dehydrogenase) gene was amplified for normalization. We used primer pair 59- CAACTACATGGTTTACATGTTC -39/59-GCCAGTGGACTCCACGAC-39 and same thermal cycling parameters (except for a change of annealing temperature to 55uC) as that of the CASP8 gene to amplify the GAPDH gene. Each sample was performed in two duplicates.Statistical AnalysisStatistical analysis was 23977191 performed using the R program (Version 2.11.1, Vienna, Austria) and a P value less than 0.05 was considered as statistically significant. Power calculations were performed by using the Quanto software [22]. Deviation from the Hardy einberg equilibrium (HWE) was assessed for each variant by using the x2-test (df = 1). Allele fre.
