AFB1 exposure years were ascertained by our previously published methods.6, 7 Briefly, AFB1 exposure years were defined as the years that each subject lived in an AFB1 exposure region, and cumulative AFB1 exposure years were calculated with the following formula: In this study, we evaluated the AFB1 exposure levels according to the AFB1 DNA adduct levels of DNA samples

from all subjects’ peripheral blood leukocytes; we used a comparative enzyme-linked immunosorbent assay, which is described in our previously published articles.7 For analysis, AFB1 DNA adduct levels were divided into three groups according to the values of the AFB1 DNA adduct levels with two cutoff points of 1.00 and 2.00 μmol/mol of DNA (the average adduct levels among controls and cases, respectively): Olaparib purchase low (≤1.00 μmol/mol of DNA), medium (1.01-2.00 μmol/mol of DNA), and high (≥2.01 μmol/mol of DNA). The gene polymorphism analysis of XPC Lys939Gln was typed by TaqMan polymerase chain reaction (PCR) on an iCycler iQ real-time PCR detection system (iQ5, Bio-Rad). The primers (5′-AGCAGCTTCCCACCTGTTC-3′ and 5′-GTGGGT GCCCCTCTAGTG-3′) and the probes (5′-FAM-CACAGCTGCTCAAAT-MGB-3′ and 5′-Hex-CTCACAGCT TCTCAAAT-MGB-3′) were obtained from the Cancer Genome buy Quizartinib Anatomy

Project SNP500 Cancer Database and were synthesized by Shanghai GeneCore BioTechnologies Co., Ltd. (Shanghai, China). PCR reactions were run in a 25-μL final volume containing 1× Premix Ex Taq (catalog number DRR039A, Takara), 0.2 μM of each probe, 0.2 μM of each primer, and 50 to 100 ng of genomic DNA. The cycling conditions were 95°C for 2 minutes and 45 cycles of 95°C for 10 seconds, 60°C for 1 minute, and 72°C for 10 seconds. Controls were included in each run, and repeated genotyping of a random 10% subset medchemexpress yielded 100% identical genotypes. Data analysis for allele discrimination was performed with the iCycler iQ software. The immunohistochemistry assay for XPC was performed according to the standard procedure (protocol 40441a, Maixin Biotechnology, Inc., Fuzhou, China). The corresponding anti-XPC polyclonal antibody

(1:200 dilution; catalog number sc-30156) and the horseradish peroxidase–conjugated secondary antibody (catalog number KIT-9707) were obtained from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA), and Maixin Biotechnology, respectively. The quality control for immunohistochemistry assays was administered with negative and positive controls. The evaluation of the staining reaction was performed according to a previously published formula26: The patients were followed for at least 0.5 years for medians and ranges. The last follow-up day was April 30, 2010, and the survival status was confirmed by patients or family contacts. In this study, the duration of survival was defined as the time from surgical resection to death or to the date on which the patient was last known to be alive.