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Abstract
Recently, a novel single nucleotide polymorphism (SNP) in the promoter of the JWA gene (−76G → C) was identified that may alter the transcription activity and thus play a role in increased risk of bladder cancer. In this study, a screen for more novel variants in the JWA exons was undertaken by using polymerase chain reaction–single-strand conformation polymorphism (PCR-SSCP) followed by a PCR-restriction fragment length polymorphism (PCR-RFLP) method and evaluating the functions of newl identified JWA −76G → C using the reporter gene assay. In addition to the −76G → C polymorphism, another novel SNP (723T → G) in exon 3 of JWA was identified. In a case-control study of these two SNPs in 413 gastric cancer and 250 esophageal squamous-cell carcinoma (ESCC) patients and 814 cancer-free controls in a Chinese population, data showed that both SNPs were associated with enhanced risk of these cancers. The reporter gene assay showed that the −76C variant allele lost its response to benzo[a]pyrene (BaP) exposure, compared to the −76G allele. In addition, the JWA −76C allele was found to be associated with increased gastric and esophageal cancer risks in this study population. Further studies are needed to substantiate the biological significance and related mechanisms underlying the associations.
Wei-Yan Tang, Lina Wang, and Chunping Li is contributed equally to this work.
This study was supported by National Key Basic Research and Development Project (973) (2002CB512900), National Natural Science Foundation of China (30471430), and Doctoral Program Funding of National Education Ministry (20040312008).
