Demethylation of the hTERT promoter in normal human gastric mucosal epithelial cells following N-methyl-N'-nitro-N-nitrosoguanidine exposure
| Autor: | Lei Wang, Yong‑Bo Cheng, Dian‑Chun Fang, Xiao‑Yan Ning, Li‑Ping Guo, Ping Yao |
|---|---|
| Rok vydání: | 2014 |
| Předmět: |
Genetics
General Neuroscience Bisulfite sequencing General Medicine Methylation Biology medicine.disease_cause Molecular biology General Biochemistry Genetics and Molecular Biology Malignant transformation CpG site medicine Telomerase reverse transcriptase Epigenetics General Pharmacology Toxicology and Pharmaceutics Carcinogenesis Demethylation |
| Zdroj: | Biomedical Reports. 3:176-178 |
| ISSN: | 2049-9442 2049-9434 |
| DOI: | 10.3892/br.2014.398 |
| Popis: | N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) is an alkylating agent that can induce gastric carcinoma. As a well-known human carcinogen, MNNG has been universally recognized as a methylating agent and is believed to act through methylation mechanism. In the present study, the epigenetic status of the human telomerase reverse transcriptase (hTERT) promoter was investigated in MNNG-treated normal human gastric mucosal epithelial cells. After 4 h exposure to MNNG at different concentrations, 6.8 and 68 µM, bisulfite sequencing polymerase chain reaction showed that five methylated cytosines outside the CpG dinucleotides in the 290-bp fragment from the hTERT promoter were demethylated and all the methylated cytosines in CpG dinucleotides remained intact. Furthermore, the epigenetic status of the target region following MNNG exposure was extremely similar to those of the BGC-823, SGC-7901 and MKN-28 lines; the three cell lines from human gastric adenocarcinoma. The result indicates that MNNG-induced demethylation in cytosines outside the CpG dinucleotides may be an early molecular lesion with the potential for impacting malignant transformation and a possible underlying carcinogenic mechanism of MNNG. Thus, it may provide another insight into the mechanisms of MNNG carcinogenesis. |
| Databáze: | OpenAIRE |
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