Glutathione S-Transferase M1, T1 and P1 Polymorphisms and Bladder Cancer Risk in Egyptians

2005 ◽  
Vol 20 (1) ◽  
pp. 69-72 ◽  
Author(s):  
A.A. Saad ◽  
P.J. O'Connor ◽  
M.H. Mostafa ◽  
N.E. Metwalli ◽  
D.P. Cooper ◽  
...  

Previous studies suggest that bladder cancer risk may vary with GST genotype but these results are inconsistent. The aim of this study was to explore whether GSTM1, GSTT1 and GSTP polymorphisms were associated with increased bladder cancer risk in an Egyptian population. GSTM1, GSTT1 and GSTP1 genotype frequencies were determined in bladder cancer cases (n=72) and healthy controls with no history of malignancies (n=82) using PCR-based techniques. The GSTT1*2 genotype was particularly associated with increased risk (OR 2.71, 95%CI 1.27–5.73) and the GSTM1*2 genotype to a lesser extent (OR 1.63, 95%CI 0.85–3.10). 18.1% of cases but only 7.3% of controls were GSTP1*B*B homozygotes (OR 2.38, 95%CI 0.83–6.87). The presence of two or more a priori at-risk genotypes was associated with increased bladder cancer risk (OR 2.42; 95%CI 1.47–3.97). These results suggest that polymorphisms in the GST genes are associated with increased risk of bladder cancer among Egyptians.

2005 ◽  
Vol 20 (1) ◽  
pp. 69-72 ◽  
Author(s):  
A.A. Saad ◽  
P.J. O'Connor ◽  
M.H. Mostafa ◽  
N.E. Metwalli ◽  
D.P. Cooper ◽  
...  

2012 ◽  
Vol 30 (15_suppl) ◽  
pp. 1503-1503 ◽  
Author(s):  
Ronac Mamtani ◽  
Kevin Haynes ◽  
Warren B. Bilker ◽  
David J. Vaughn ◽  
Brian L. Strom ◽  
...  

1503 Background: The US Food and Drug Administration and other regulatory agencies recently warned prescribers that use of pioglitazone, a thiazolidinedione (TZD), may increase the risk of bladder cancer. France and Germany removed the drug from their markets, although the rest of Europe did not. However, no information was available about the risk from alternative TZDs. We aimed to compare bladder cancer risk over time with use of TZDs relative to sulfonylureas (SUs), and between pioglitazone and rosiglitazone. Methods: We conducted a cohort study of patients with type 2 diabetes who initiated treatment with a TZD or SU using The Health Improvement Network (2000-2010), a UK general practitioner medical record database. Incident cancers within the database were identified. We computed hazard ratios (HRs) of bladder cancer for TZDs in comparison to the reference group of SU users. Results: There were 60 incident diagnoses of bladder cancer in the TZD cohort (n=18,459) and 137 in the SU cohort (n=41,396). There was no significant difference in bladder cancer risk between the cohorts (HR 0·93, [95% CI 0·68-1·29]), but most use was short-term use. In contrast, the risk of bladder cancer increased with increasing time since initiation of TZD versus SU therapy (HRs 1·15, 1·40, and 1·72 for 3-4, 4-5, and ≥ 5 years, respectively; P-trend=0·033). Bladder cancer risk also increased with increasing time since initiation of pioglitazone (P-trend<0·001) and rosiglitazone (P-trend=0·006). Direct comparison of pioglitazone to rosiglitazone did not demonstrate significant differences in cancer risk with increasing time since initiation (P-trend=0·12) or duration of therapy (P-trend=0·75). Conclusions: Long-term TZD therapy is associated with an increased risk of bladder cancer, which appears to be a class effect.


2014 ◽  
Vol 23 (1) ◽  
pp. 58-61 ◽  
Author(s):  
Koray Erdurak ◽  
Pinar E. Dundar ◽  
Beyhan C. Ozyurt ◽  
Eva Negri ◽  
Carlo La Vecchia ◽  
...  

Author(s):  
Stella Koutros ◽  
Kathy L. Decker ◽  
Dalsu Baris ◽  
Larissa A. Pardo ◽  
Alison Johnson ◽  
...  

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