Sasamoto Hiromi, Nagasaka Takeshi, Notohara Kenji, Ozaki Kazuhide, Isozaki Hiroshi, Tanaka Noriaki, Matsubara Nagahide
Department of Gastroenterological Surgery and Surgical Oncology, Okayama University Graduate School of Medicine and Dentistry, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
Int J Oncol. 2004 Nov;25(5):1273-8.
H19 and IGF2 genes are imprinted genes and expressed differently depending on whether they are carried by a chromosome of maternal or paternal origin; H19 is expressed only from the maternal allele and IGF2 only from the paternally inherited allele. The upstream promoter region of H19 has the imprinting-control region (ICR) or CTCF binding sites, where the methylation status of this region is critical to the regulation of imprinting of the H19/IGF2 locus located in chromosome 11p15. There are various reports on imprinting disorders in this region. In colorectal cancer aberrant biallelic methylation of CTCF binding site has been reported, and aberrant hypomethylation of this region in bladder cancer. Thus, certain human neoplasms have either hyper- or hypo-methylation in the ICR. Hence it is still difficult to analyze allele-specific methylation disorder of the region, or differentially methylated regions (DMR), locate upstream of H19. Here we report a new method, which could distinguish paternal epigenetic or maternal epigenetic pattern by a single PCR assay, to combine methylation-specific PCR and PCR with confronting two-pair primers (MSP-CTPP). Using this method, we investigated the region close to H19 ICR in 161 colorectal cancer and 65 gastric cancer cases.
H19和IGF2基因是印记基因,其表达取决于它们是由母源还是父源染色体携带,表现出差异;H19仅从母本等位基因表达,而IGF2仅从父本遗传的等位基因表达。H19的上游启动子区域具有印记控制区(ICR)或CTCF结合位点,该区域的甲基化状态对于位于11p15染色体上的H19/IGF2基因座的印记调控至关重要。关于该区域的印记紊乱有各种报道。在结直肠癌中,已报道CTCF结合位点存在异常双等位基因甲基化,在膀胱癌中该区域存在异常低甲基化。因此,某些人类肿瘤在ICR中存在高甲基化或低甲基化。因此,分析H19上游区域的等位基因特异性甲基化紊乱或差异甲基化区域(DMR)仍然很困难。在此,我们报告一种新方法,该方法可通过单一PCR检测区分父本表观遗传或母本表观遗传模式,即将甲基化特异性PCR与两对引物对PCR(MSP-CTPP)相结合。使用该方法,我们研究了161例结直肠癌和65例胃癌病例中靠近H19 ICR的区域。