Matches in SemOpenAlex for { <https://semopenalex.org/work/W2173921146> ?p ?o ?g. }
- W2173921146 endingPage "733" @default.
- W2173921146 startingPage "726" @default.
- W2173921146 abstract "Transcriptional silencing induced by hypermethylation of CpG islands in the promoter regions of genes is believed to be an important mechanism of carcinogenesis in human cancers including gastric cancer. A number of reports on methylation of various genes in gastric cancer have been published, but most of these studies focused on cancer tissues or only a single gene. In this study, we determined the promoter hypermethylation status and mRNA expression of 4 genes: p16, Runx3, DAPK and CHFR.Methylation-specific polymerase chain reaction (MSP) was used to determine the methylation status of p16, Runx3, DAPK and CHFR gene promoters in cancer and adjacent normal gastric mucosa specimens from 70 patients with gastric cancer, as well as normal gastric biopsy samples from 30 people without cancer serving as controls. In addition, the mRNA expression of p16, Runx3, DAPK and CHFR was investigated in 34 gastric cancer patients by RT-PCR. Bisulfite DNA sequence analysis was applied to check the positive samples detected by MSP.When carcinoma specimens were compared with adjacent normal gastric mucosa samples, a significant increase in promoter methylation of p16, Runx3, DAPK and CHFR was observed, while all 30 histologically normal gastric specimens were methylation free for all 4 genes. The methylation rate of the 4 genes increased from normal stomach tissue to tumor-adjacent gastric mucosa to gastric cancer tissue. Concurrent methylation in 2 or more genes was found in 22.9% of tumor-adjacent normal gastric mucosa and 75.7% of cancer tissues. No correlation was found between hypermethylation and other clinicopathological parameters such as sex, age, and tumor location. However, the frequency of DAPK and CHFR methylation in cancer tissues was significantly associated with the extent of differentiation and lymph node metastasis (P < 0.05) and the frequency of Runx3 methylation was significantly associated with tumor size (P < 0.05). Weak expression and loss of expression of the 4 genes was observed in cancer tissues and was significantly associated with promoter hypermethylation (P < 0.05).Promoter hypermethylation of p16, Runx3, DAPK and CHFR is frequent in gastric cancer. DAPK and CHFR promoter hypermethylation may be an important help in evaluating the differentiation grade and lymph node status of gastric cancer. Weak gene expression and loss of gene expression due to promoter hypermethylation may be a cancer-specific event." @default.
- W2173921146 created "2016-06-24" @default.
- W2173921146 creator A5004511329 @default.
- W2173921146 creator A5011237730 @default.
- W2173921146 creator A5019853987 @default.
- W2173921146 creator A5024475510 @default.
- W2173921146 creator A5032802567 @default.
- W2173921146 creator A5065087364 @default.
- W2173921146 creator A5067864343 @default.
- W2173921146 creator A5068301710 @default.
- W2173921146 creator A5077763328 @default.
- W2173921146 creator A5088868725 @default.
- W2173921146 date "2010-09-01" @default.
- W2173921146 modified "2023-09-26" @default.
- W2173921146 title "Promoter methylation of p16, Runx3, DAPK and CHFR genes is frequent in gastric carcinoma" @default.
- W2173921146 cites W1556996865 @default.
- W2173921146 cites W1579447084 @default.
- W2173921146 cites W1977848387 @default.
- W2173921146 cites W1979125899 @default.
- W2173921146 cites W1979751052 @default.
- W2173921146 cites W1986222497 @default.
- W2173921146 cites W1989478892 @default.
- W2173921146 cites W1990974448 @default.
- W2173921146 cites W1994465394 @default.
- W2173921146 cites W2004078197 @default.
- W2173921146 cites W2005850806 @default.
- W2173921146 cites W2007715266 @default.
- W2173921146 cites W2009335081 @default.
- W2173921146 cites W2015604066 @default.
- W2173921146 cites W2018045309 @default.
- W2173921146 cites W2018358825 @default.
- W2173921146 cites W2022375598 @default.
- W2173921146 cites W2026062907 @default.
- W2173921146 cites W2028779612 @default.
- W2173921146 cites W2029484950 @default.
- W2173921146 cites W2040149948 @default.
- W2173921146 cites W2040257851 @default.
- W2173921146 cites W2043033879 @default.
- W2173921146 cites W2046509449 @default.
- W2173921146 cites W2051446559 @default.
- W2173921146 cites W2056682844 @default.
- W2173921146 cites W2060146332 @default.
- W2173921146 cites W2066848701 @default.
- W2173921146 cites W2073219326 @default.
- W2173921146 cites W2101995865 @default.
- W2173921146 cites W2106651084 @default.
- W2173921146 cites W2109877837 @default.
- W2173921146 cites W2120436117 @default.
- W2173921146 cites W2125034361 @default.
- W2173921146 cites W2128146359 @default.
- W2173921146 cites W2138544437 @default.
- W2173921146 cites W2161005330 @default.
- W2173921146 cites W2161486169 @default.
- W2173921146 cites W2178580292 @default.
- W2173921146 cites W4229952372 @default.
- W2173921146 doi "https://doi.org/10.1177/030089161009600515" @default.
- W2173921146 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21302620" @default.
- W2173921146 hasPublicationYear "2010" @default.
- W2173921146 type Work @default.
- W2173921146 sameAs 2173921146 @default.
- W2173921146 citedByCount "34" @default.
- W2173921146 countsByYear W21739211462012 @default.
- W2173921146 countsByYear W21739211462013 @default.
- W2173921146 countsByYear W21739211462014 @default.
- W2173921146 countsByYear W21739211462015 @default.
- W2173921146 countsByYear W21739211462016 @default.
- W2173921146 countsByYear W21739211462017 @default.
- W2173921146 countsByYear W21739211462018 @default.
- W2173921146 countsByYear W21739211462019 @default.
- W2173921146 countsByYear W21739211462020 @default.
- W2173921146 countsByYear W21739211462021 @default.
- W2173921146 countsByYear W21739211462022 @default.
- W2173921146 countsByYear W21739211462023 @default.
- W2173921146 crossrefType "journal-article" @default.
- W2173921146 hasAuthorship W2173921146A5004511329 @default.
- W2173921146 hasAuthorship W2173921146A5011237730 @default.
- W2173921146 hasAuthorship W2173921146A5019853987 @default.
- W2173921146 hasAuthorship W2173921146A5024475510 @default.
- W2173921146 hasAuthorship W2173921146A5032802567 @default.
- W2173921146 hasAuthorship W2173921146A5065087364 @default.
- W2173921146 hasAuthorship W2173921146A5067864343 @default.
- W2173921146 hasAuthorship W2173921146A5068301710 @default.
- W2173921146 hasAuthorship W2173921146A5077763328 @default.
- W2173921146 hasAuthorship W2173921146A5088868725 @default.
- W2173921146 hasConcept C104317684 @default.
- W2173921146 hasConcept C119056186 @default.
- W2173921146 hasConcept C121608353 @default.
- W2173921146 hasConcept C126322002 @default.
- W2173921146 hasConcept C140173407 @default.
- W2173921146 hasConcept C142724271 @default.
- W2173921146 hasConcept C150194340 @default.
- W2173921146 hasConcept C153911025 @default.
- W2173921146 hasConcept C189235521 @default.
- W2173921146 hasConcept C190727270 @default.
- W2173921146 hasConcept C2779422922 @default.
- W2173921146 hasConcept C2781443798 @default.
- W2173921146 hasConcept C33288867 @default.
- W2173921146 hasConcept C502942594 @default.