Abstract
Objectives To detect hypermethylation status of the 5'CpG island locating in the promoter re - glon of RUNX3 gene and the expression level of their mRNA and protein in bladder transitional cell carcinoma (BTCC).Methods Using methylation - specific PCR(MSP) technique to detect methylation status of RUNX3 gene in BTCC,and to detect their mRNA and protein expression level by RT - PCR and Westem blot method.Re - suits The frequenee of Promoter methylation of RUNX3 gene Was 46.9%(15/32) in BTCC tissues,but it Was not found in normal bladder tissues.The frequenee of Promoter methylation wag increased with the increasing tumor grade and stage(P<O.01).In 15 patients with the aberrant Promoter methyiation,14 patients shown the loss ex - pression of RUNX3 gene(r=0.6472,P=0.012).The expression of RUNX3 mRNA and protein in the normal bladder tissues and BTCC tissue were93.8%(30/32),34.4%(11/32),respectively(P<0.01).It Wag cor - related with its clinical stages and pathological grades(P<0.05).Conclusions Hypermethylation can inacti - vate the transcription of RUNX3 and reduce its protein expression.It may be a considerable mechanism which leads to oncogenesis,metastasis of BTCC. Key words: Careinoma,Transitional Cell; Bladder Neoplagmsl; Operon; Methylation
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