Yamada Yasushi, Watanabe Masatoshi, Yamanaka Mikio, Hirokawa Yoshifumi, Suzuki Hiroyoshi, Takagi Akimitsu, Matsuzaki Takeshi, Sugimura Yoshiki, Yatani Ryuichi, Shiraishi Taizo
Second Department of Pathology, Mie University Faculty of Medicine, Tsu 514-8507, Japan.
Cancer Sci. 2003 Jun;94(6):536-9. doi: 10.1111/j.1349-7006.2003.tb01479.x.
Transcriptional silencing of cancer-related genes by DNA methylation is observed in various cancers. To identify genes controlled by methylation in prostate cancer, we used cDNA microarray analysis to investigate gene expression in prostate cancer cell lines LNCaP and DU145 treated with a methyltransferase inhibitor alone or together with a histone deacetylase inhibitor. We detected significant changes (3.4-5.7%) in gene expression in prostate cancer cell lines with the drug treatments. Among the affected genes, that for the vascular endothelial growth factor receptor 1 (VEGFR-1) was re-expressed in LNCaP and DU145 after the drug treatments. Bisulfite sequencing revealed the promoter and exon 1 of the VEGFR-1 to be hypermethylated in the cell lines. These results support the idea that methylation is associated with loss of VEGFR-1 mRNA expression in prostate cancer cell lines. Combined bisulfite restriction analysis (COBRA) showed the gene to be methylated in 24 (38.1%) of 63 primary local prostate cancer samples, while in all 13 benign prostate samples it was not. These findings indicate that methylation of VEGFR-1 is related with prostatic carcinogenesis.
在多种癌症中均观察到DNA甲基化导致癌症相关基因的转录沉默。为了鉴定前列腺癌中受甲基化调控的基因,我们使用cDNA微阵列分析来研究单独使用甲基转移酶抑制剂或与组蛋白脱乙酰酶抑制剂联合处理的前列腺癌细胞系LNCaP和DU145中的基因表达。我们检测到药物处理后的前列腺癌细胞系中基因表达有显著变化(3.4 - 5.7%)。在受影响的基因中,血管内皮生长因子受体1(VEGFR - 1)的基因在药物处理后的LNCaP和DU145中重新表达。亚硫酸氢盐测序显示VEGFR - 1的启动子和外显子1在这些细胞系中高度甲基化。这些结果支持甲基化与前列腺癌细胞系中VEGFR - 1 mRNA表达缺失相关的观点。联合亚硫酸氢盐限制分析(COBRA)显示该基因在63例原发性局限性前列腺癌样本中的24例(38.1%)中发生甲基化,而在所有13例良性前列腺样本中均未发生甲基化。这些发现表明VEGFR - 1的甲基化与前列腺癌发生有关。