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培养的和原发性结直肠癌中 hedgehog 配体的独特表达模式与它们启动子的异常甲基化有关。

Distinct expression patterns of hedgehog ligands between cultured and primary colorectal cancers are associated with aberrant methylation of their promoters.

机构信息

Department of Gastroenterology, The People's Hospital of Deyang City, Sichuan, China.

出版信息

Mol Cell Biochem. 2010 Apr;337(1-2):185-92. doi: 10.1007/s11010-009-0298-8. Epub 2009 Oct 24.

Abstract

Ligand-dependent activation of the Hedgehog (Hh) pathway in colorectal cancers (CRCs) is controversial, and the regulation mechanism of Hh ligands expression remains to be determined. In the present study, the mRNA expressions of Sonic hedgehog (SHH), Indian hedgehog (IHH), Patched, Smoothened, and Gli1 were examined in four cultured colon cancer cell lines by reverse transcription-PCR. Moreover, ligands mRNA expression (SHH and IHH) were examined by reverse transcription-PCR, and SHH protein expression by immunohistochemistry in 25 primary CRCs. The methylation status of SHH and IHH was also investigated by bisulfate sequencing or methylation specific PCR. IHH mRNA was completely absent in cell lines studied, and expressed at a very low level or not expressed at all in primary CRCs. Methylation analysis revealed that IHH promoter was hypermethylated in colon cancer cell lines. Absence of SHH mRNA expression and hypermethylation of its promoter was also observed in colon cancer cell lines. However, high level expression of SHH and hypomethylation of its promoter was detected in primary CRCs. In conclusion, ligand dependent activity of Hh pathway is inactive in cultured colon cancer cells correlating to ligands hypermethylation. In contrast, SHH overexpression, possible consequence of promoter hypomethylation, could play a role in the carcinogenesis of primary CRCs.

摘要

Hedgehog (Hh) 通路在结直肠癌中的配体依赖性激活存在争议,Hh 配体表达的调控机制仍有待确定。在本研究中,通过逆转录-PCR 检测了四种培养的结肠癌细胞系中 Sonic hedgehog (SHH)、Indian hedgehog (IHH)、Patched、Smoothened 和 Gli1 的 mRNA 表达。此外,通过逆转录-PCR 检测了配体 mRNA 表达 (SHH 和 IHH),并通过免疫组织化学检测了 25 例原发性 CRC 中的 SHH 蛋白表达。还通过亚硫酸氢盐测序或甲基化特异性 PCR 研究了 SHH 和 IHH 的甲基化状态。在所研究的细胞系中,IHH mRNA 完全缺失,在原发性 CRC 中表达水平极低或根本不表达。甲基化分析显示 IHH 启动子在结肠癌细胞系中高度甲基化。在结肠癌细胞系中也观察到 SHH mRNA 表达缺失和其启动子的高度甲基化。然而,在原发性 CRC 中检测到 SHH 的高水平表达和其启动子的低甲基化。总之,与配体高甲基化相关,培养的结肠癌细胞中 Hh 通路的配体依赖性活性是不活跃的。相比之下,SHH 的过表达,可能是启动子低甲基化的结果,可能在原发性 CRC 的发生中起作用。

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