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The results of the association of TP53 with other genes in bladder cancer cells were then analyzed by Student's t-test and the hypergeometric distribution. Injection of anti-caspase-3 (Bcl-XL) was accompanied by an increase in the number of apoptotic in vivo xenograft tumors, and inhibited the expression of Bcl-XL. Intracellular and extracellular caspase-3 activation was measured by western blotting. Our data indicated that expression of TSG101 significantly reduced tumorigenicity and cell growth in vitro and in vivo. We further investigated the relationship between caspase-3 and TSG101 and found that treatment of TSG101-positive tumor cells with anti-caspase-3 (Bcl-XL) significantly blocked the expression of Bcl-XL. This finding suggested that the effects of TSG101 on tumorigenesis were associated with cell apoptosis.
Intracellular and extracellular caspase-3 activation was measured by western blotting. Our data indicated that expression of TSG101 significantly reduced tumorigenicity and cell growth in vitro and in vivo. We further investigated the relationship between caspase-3 and TSG101 and found that treatment of TSG101-positive tumor cells with anti-caspase-3 (Bcl-XL) significantly blocked the expression of Bcl-XL. This finding suggested that the effects of TSG101 on tumorigenesis were associated with cell apoptosis.
Relative Expression Levels of TSG101, Bcl-XL, and Caspase-3 in TSG101 Overexpression and Knockdown Cell Lines and Normal Cells.
The results of the association of TP53 with other genes in bladder cancer cells were then analyzed by Student's t-test and the hypergeometric distribution. The association between TSG101 protein expression and tumor clinicopathological parameters revealed that the levels of TSG101 were associated with the pathological grade, tumor size, and tumor invasion. The results of the RT-PCR and western blotting analyses showed that TSG101 was upregulated in bladder cancer cell lines and patient samples (P 0b46394aab
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