Fibulin 1 is downregulated through promoter hypermethylation in gastric cancer

التفاصيل البيبلوغرافية
العنوان: Fibulin 1 is downregulated through promoter hypermethylation in gastric cancer
المؤلفون: Ng, EKO, Leung, WK, Sung, JJY, Chan, FKL, Liu, X, Wong, YP, Yu, J, Siu, JMT, Cheng, YY, Jin, H
المصدر: British Journal of Cancer
بيانات النشر: Springer Science and Business Media LLC, 2008.
سنة النشر: 2008
مصطلحات موضوعية: Male, Aza Compounds, Cancer Research, gastric cancer, digestive, oral, and skin physiology, Calcium-Binding Proteins, Down-Regulation, Genetics and Genomics, DNA Methylation, tumour suppressor gene, FBLN1, digestive system diseases, Up-Regulation, Gene Expression Regulation, Neoplastic, Oncology, Stomach Neoplasms, Cell Line, Tumor, Humans, Female, methylation, Promoter Regions, Genetic, Aged, Cell Proliferation
الوصف: Tumour suppressor genes (TSGs) were frequently inactivated through promoter hypermethylation in gastric carcinoma as well as pre-malignant gastric lesions, suggesting that promoter hypermethylation can be used as a marker to define novel TSGs and also biomarkers for early detection of gastric cancer. In an effort to search for such genes aberrantly methylated in gastric cancer development, fibulin 1 (FBLN1) was found as a candidate TSG epigenetically downregulated in gastric cancer. FBLN1 expression was downregulated in all of gastric cancer cell lines used (100%, 7 out of 7) and the primary gastric carcinoma tissues (84%, 86 out of 102) and significantly restored after pharmacological demethylation. Hypermethylation of the FBLN1 promoter was frequently (71%, 5 out of 7) detected in gastric cancer cell lines and primary gastric carcinoma tissues. Ectopic expression of FBLN1 led to the growth inhibition of gastric cancer cells through the induction of apoptosis. In summary, FBLN1 was identified as a novel candidate TSG epigenetically downregulated in gastric cancer. © 2008 Cancer Research.
published_or_final_version
تدمد: 1532-1827
0007-0920
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d638674b829f4669652a75b888961a04
https://doi.org/10.1038/sj.bjc.6604760
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....d638674b829f4669652a75b888961a04
قاعدة البيانات: OpenAIRE