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DisGeNET

Id Subject Object Predicate Lexical cue
T0 687-692 gene:1910 denotes EDNRB
T1 700-714 disease:C0005684 denotes bladder cancer
T2 687-692 gene:1910 denotes EDNRB
T3 700-714 disease:C0699885 denotes bladder cancer
R1 T0 T1 associated_with EDNRB,bladder cancer
R2 T2 T3 associated_with EDNRB,bladder cancer

DisGeNET5_gene_disease

Id Subject Object Predicate Lexical cue
15569975-3#168#173#gene1910 687-692 gene1910 denotes EDNRB
15569975-3#181#195#diseaseC0005684 700-714 diseaseC0005684 denotes bladder cancer
15569975-3#181#195#diseaseC0005695 700-714 diseaseC0005695 denotes bladder cancer
15569975-3#181#195#diseaseC0699885 700-714 diseaseC0699885 denotes bladder cancer
15569975-8#31#35#gene7015 1661-1665 gene7015 denotes TERT
15569975-8#63#77#diseaseC0005684 1693-1707 diseaseC0005684 denotes bladder cancer
15569975-8#63#77#diseaseC0005695 1693-1707 diseaseC0005695 denotes bladder cancer
15569975-8#63#77#diseaseC0699885 1693-1707 diseaseC0699885 denotes bladder cancer
168#173#gene1910181#195#diseaseC0005684 15569975-3#168#173#gene1910 15569975-3#181#195#diseaseC0005684 associated_with EDNRB,bladder cancer
168#173#gene1910181#195#diseaseC0005695 15569975-3#168#173#gene1910 15569975-3#181#195#diseaseC0005695 associated_with EDNRB,bladder cancer
168#173#gene1910181#195#diseaseC0699885 15569975-3#168#173#gene1910 15569975-3#181#195#diseaseC0699885 associated_with EDNRB,bladder cancer
31#35#gene701563#77#diseaseC0005684 15569975-8#31#35#gene7015 15569975-8#63#77#diseaseC0005684 associated_with TERT,bladder cancer
31#35#gene701563#77#diseaseC0005695 15569975-8#31#35#gene7015 15569975-8#63#77#diseaseC0005695 associated_with TERT,bladder cancer
31#35#gene701563#77#diseaseC0699885 15569975-8#31#35#gene7015 15569975-8#63#77#diseaseC0699885 associated_with TERT,bladder cancer

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 107-497 OBJECTIVE denotes There is increasing evidence for a fundamental role for epigenetic silencing of apoptotic pathways in cancer. Changes in DNA methylation can be detected with a high degree of sensitivity, so we used the MethyLight assay to determine how methylation patterns of apoptosis-associated genes change during bladder carcinogenesis and whether DNA methylation could be detected in urine sediments.
T2 519-964 METHODS denotes We analyzed the methylation status of the 5' regions of 12 apoptosis-associated genes (ARF, FADD, TNFRSF21, BAX, LITAF, DAPK, TMS-1, BCL2, RASSF1A, TERT, TNFRSF25, and EDNRB) in 18 bladder cancer cell lines, 127 bladder cancer samples, and 37 samples of adjacent normal bladder mucosa using the quantitative MethyLight assay. We also analyzed the methylation status in urine sediments of 20 cancer-free volunteers and 37 bladder cancer patients.
T3 974-1862 RESULTS denotes The 5' regions of DAPK, BCL2, TERT, RASSFIA, and TNFRSF25 showed significant increases in methylation levels when compared with nonmalignant adjacent tissue (P < or = 0.01). Methylation levels of BCL2 were significantly associated with tumor staging and grading (P < or = 0.01), whereas methylation levels of RASSF1A and ARF were only associated with tumor stage (P < or = 0.04), and TERT methylation and EDNRB methylation were predictors of tumor grade (P < or = 0.02). To investigate clinical usefulness for noninvasive bladder cancer detection, we further analyzed the methylation status of the markers in urine samples of patients with bladder cancer. Methylation of DAPK, BCL2, and TERT in urine sediment DNA from bladder cancer patients was detected in the majority of samples (78%), whereas they were unmethylated in the urine sediment DNA from age-matched cancer-free individuals.
T4 1876-2412 CONCLUSIONS denotes Our results indicate that methylation of the 5' region of apoptosis-associated genes is a common finding in patients with bladder carcinoma. The ability to detect methylation not only in bladder tissue, but also in urine sediments, suggests that methylation markers are promising tools for noninvasive detection of bladder cancers. Our results also indicate that some methylation markers, such as those in regions of RASSF1A and TNFRSF25, might be of limited use for detection because they are also methylated in normal bladder tissues.