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Gene expression study related with the intrinsic pathway of apoptosis in bladder cancer by real-time PCR technique
Author(s) -
D.F. Barione,
F.S.N. Lizarte,
Paulo Cézar Novais,
Camila Albuquerque Melo de Carvalho,
F.C.B. Valeri,
Fernanda Maris Peria,
Harley Francisco de Oliveira,
Dalila Lucíola Zanette,
Wilson A. Silva,
Adauto José Cologna,
Rodolfo Borges dos Reis,
Sílvio Tucci,
Ana Cláudia Martins,
Daniela Pretti da Cunha Tirapelli,
Luiz Fernando Tirapelli
Publication year - 2013
Publication title -
genetics and molecular research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.356
H-Index - 48
ISSN - 1676-5680
DOI - 10.4238/2013.april.2.4
Subject(s) - xiap , survivin , apoptosis , gene expression , gene , bladder cancer , cytochrome c , cancer research , cancer , real time polymerase chain reaction , biology , caspase 9 , caspase 3 , medicine , caspase , genetics , programmed cell death
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.

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