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Gene expression study related with the intrinsic pathway of apoptosis in bladder cancer by real-time PCR technique.

Authors :
Barione DF
Lizarte FS
Novais PC
de Carvalho CA
Valeri FC
Peria FM
de Oliveira HF
Zanette DL
Silva WA Jr
Cologna AJ
Reis RB
Tucci S Jr
Martins AC
Tirapelli DP
Tirapelli LF
Source :
Genetics and molecular research : GMR [Genet Mol Res] 2013 Apr 02; Vol. 12 (2), pp. 878-86. Date of Electronic Publication: 2013 Apr 02.
Publication Year :
2013

Abstract

We examined the expression of anti-apoptotic genes (XIAP and Bcl-2) and apoptotic genes (cytochrome c, caspase-9, Apaf-1) in tissue samples of patients with superficial bladder cancer. Thirty-two bladder cancer tissue samples (8 papillary urothelial neoplasm of low malignant potential, 10 low-grade, and 14 high-grade) and 8 normal bladder tissue samples from necropsy were used for the study of gene expression by real-time PCR analysis. Analysis of the expression of apoptotic gene constituents of an apoptosome demonstrated an increase in Apaf-1 expression in the three tumor grades when compared with the control (P < 0.01, P < 0.05, and P < 0.01), low expression of caspase-9 in all groups (P < 0.05), and an increase in cytochrome c expression in all tumor grades in relation to the control, although without statistically significant difference. The expression of anti-apoptotic genes revealed an increase in XIAP expression in all tumor grades in relation to the control, although without statistically significant difference, and low expression of Bcl-2 in all tumor grades and the control (P < 0.05). The results proved that there is low evidence of apoptotic activity by the intrinsic pathway, demonstrated by the low expression of caspase-9 and considerable increase in XIAP expression, which may render these genes potential therapeutic targets in bladder cancer treatment.

Details

Language :
English
ISSN :
1676-5680
Volume :
12
Issue :
2
Database :
MEDLINE
Journal :
Genetics and molecular research : GMR
Publication Type :
Academic Journal
Accession number :
23613234
Full Text :
https://doi.org/10.4238/2013.April.2.4