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口腔癌细胞中Krüppel样因子4的表达及基因启动子的高甲基化

Krüppel-like factor 4 expression in oral carcinoma cells and hypermethylation at the gene promoter.

作者信息

Yamaguchi Ayumi, Kuroyama Karen, Tokura Ayana, Saito Atsushi, Arikawa Huhga, Hasebe Takahisa, Usui Dai, Yamaguchi Kosuke, Chiba Tadashige, Imai Kazushi

机构信息

School of Life Dentistry at Tokyo, The Nippon Dental University, 1-9-20, Chiyoda-ku, Fujimi, Tokyo, 102-8159, Japan.

Department of Biochemistry, School of Life Dentistry at Tokyo, The Nippon Dental University, 1-9-20 Chiyoda-ku, Fujimi, Tokyo, 102-8159, Japan.

出版信息

BMC Oral Health. 2016 Feb 4;16:13. doi: 10.1186/s12903-016-0172-5.

Abstract

BACKGROUND

Krüppel-like factor 4 (KLF4) is a transcription factor regulating proliferation-differentiation balance of epithelium, and down-regulated in less-differentiated and advanced oral carcinomas. Although the expression is inactivated by the promoter hypermethylation in malignant tumor cells, it remains unknown in oral carcinoma cells.

METHODS

Genomic DNA isolated from nine different oral carcinoma cell lines and a normal keratinocyte line was treated with sodium bisulfite, and methylation at KLF4 gene promoter was determined by PCR direct-sequence analysis. KLF4 expression in cells cultured with or without demethylation reagent was monitored by quantitative real-time PCR and immunoblot.

RESULTS

A 237-bp promoter region spanning - 718 and - 482 of KLF4 gene was hypermethylated in oral carcinoma cells that express KLF4 at a low level, but the methylation was infrequent in cells expressing KLF4 high amount. The downstream region from - 481 to +192 was not methylated in any cell lines. Demethylation treatment of cells up-regulated the expression at mRNA and protein levels.

CONCLUSION

This study demonstrated that hypermethylation at a narrow range of the promoter region down-regulates KLF4 expression, and suggests that the loss of expression by the hypermethylation contributes to oral carcinoma progression.

摘要

背景

Krüppel样因子4(KLF4)是一种调节上皮细胞增殖-分化平衡的转录因子,在低分化和晚期口腔癌中表达下调。尽管在恶性肿瘤细胞中其表达因启动子高甲基化而失活,但在口腔癌细胞中情况仍不清楚。

方法

从9种不同的口腔癌细胞系和1种正常角质形成细胞系中分离基因组DNA,用亚硫酸氢钠处理,通过PCR直接测序分析测定KLF4基因启动子的甲基化情况。用定量实时PCR和免疫印迹法监测用或不用去甲基化试剂培养的细胞中KLF4的表达。

结果

在低水平表达KLF4的口腔癌细胞中,KLF4基因跨度为-718至-482的237 bp启动子区域发生高甲基化,但在高表达KLF4的细胞中这种甲基化不常见。-481至+192的下游区域在任何细胞系中均未发生甲基化。对细胞进行去甲基化处理可上调mRNA和蛋白质水平的表达。

结论

本研究表明,启动子区域狭窄范围内的高甲基化下调KLF4表达,并提示高甲基化导致的表达缺失促进口腔癌进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8f9/4743192/8c67829871a5/12903_2016_172_Fig1_HTML.jpg

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