Kim Kyung-Hee, Choi Jin-Sung, Kim Il-Jin, Ku Ja-Lok, Park Jae-Gahb
Laboratory of Cell Biology, Cancer Research Institute, Seoul National University College of Medicine, 28 Yongon-dong, Chongno-gu, Seoul 110-744, Korea.
World J Gastroenterol. 2006 Sep 21;12(35):5651-7. doi: 10.3748/wjg.v12.i35.5651.
To verify the expression and methylation status of the MAGE-A1 and MAGE-A3 genes in colorectal cancer tissues and cancer cell lines.
We evaluated promoter demethylation status of the MAGE-A1 and MAGE-A3 genes by RT-PCR analysis and methylation-specific PCR (MS-PCR), as well as sequencing analysis, after sodium bisulfite modification in 32 colorectal cancer cell lines and 87 cancer tissues.
Of the 32 cell lines, MAGE-A1 and MAGE-A3 expressions were observed in 59% and 66%, respectively. Subsequent to sodium bisulfite modification and MS-PCR analysis, the promoter hypomethylation of MAGE-A1 and MAGE-A3 was confirmed in both at 81% each. Promoter hypomethylation of MAGE-A1 and MAGE-A3 in colorectal cancer tissues was observed in 43% and 77%, respectively. Hypomethylation of MAGE-A1 and MAGE-A3 genes in corresponding normal tissues were observed in 2% and 6%, respectively.
The promoter hypomethylation of MAGE genes up-regulates its expression in colorectal carcinomas as well as in gastric cancers and might play a significant role in the development and progression of human colorectal carcinomas.
验证MAGE - A1和MAGE - A3基因在结直肠癌组织及癌细胞系中的表达及甲基化状态。
在32个结直肠癌细胞系和87个癌组织中,通过亚硫酸氢钠修饰后的逆转录聚合酶链反应(RT-PCR)分析、甲基化特异性PCR(MS-PCR)以及测序分析,评估MAGE - A1和MAGE - A3基因的启动子去甲基化状态。
在32个细胞系中,分别有59%和66%观察到MAGE - A1和MAGE - A3的表达。亚硫酸氢钠修饰及MS-PCR分析后,证实MAGE - A1和MAGE - A3的启动子低甲基化在两者中均为81%。在结直肠癌组织中,分别有43%和77%观察到MAGE - A1和MAGE - A3的启动子低甲基化。在相应正常组织中,分别有2%和6%观察到MAGE - A1和MAGE - A3基因的低甲基化。
MAGE基因的启动子低甲基化在结直肠癌以及胃癌中上调其表达,可能在人类结直肠癌的发生发展中起重要作用。