TY - JOUR
T1 - Atorvastatin
T2 - A potential chemopreventive agent in bladder cancer
AU - Kamat, Ashish M.
AU - Nelkin, Gina M.
N1 - Funding Information:
This study funded by NCI/NIH grant 1P50 CA91846-01 (GU SPORE).
PY - 2005/12
Y1 - 2005/12
N2 - Objectives. To evaluate a commonly used 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor - atorvastatin - for potential activity against human bladder cancer. Patients with bladder cancer often have concomitant hyperlipidemia and cardiac disease due to common risk factors such as smoking and advanced age. As such, they are often prescribed HMG-CoA reductase inhibitors (statins), which have been suggested to affect tumor growth patterns. Methods. Two human transitional cell carcinoma cell lines - RT4 and KU-7 - were exposed to atorvastatin at concentrations from 0 (control) to 100 μM for 48 or 72 hours. The effects on cell proliferation, DNA synthesis, and apoptosis were respectively evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetric assay and the thymidine incorporation assay and by quantifying DNA fragmentation by propidium iodide fluorescence and flow cytometry. Results. Atorvastatin inhibited cell proliferation and DNA synthesis in both bladder cancer cell lines. This led to significant cytotoxicity as demonstrated by DNA fragmentation and induction of apoptosis. Conclusions. Atorvastatin exhibits significant antiproliferative and pro-apoptotic activity in human bladder cancer cells. This, coupled with its established clinical safety profile, provides a rationale for its use as a potential chemopreventive agent against bladder cancer.
AB - Objectives. To evaluate a commonly used 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor - atorvastatin - for potential activity against human bladder cancer. Patients with bladder cancer often have concomitant hyperlipidemia and cardiac disease due to common risk factors such as smoking and advanced age. As such, they are often prescribed HMG-CoA reductase inhibitors (statins), which have been suggested to affect tumor growth patterns. Methods. Two human transitional cell carcinoma cell lines - RT4 and KU-7 - were exposed to atorvastatin at concentrations from 0 (control) to 100 μM for 48 or 72 hours. The effects on cell proliferation, DNA synthesis, and apoptosis were respectively evaluated using the 3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide colorimetric assay and the thymidine incorporation assay and by quantifying DNA fragmentation by propidium iodide fluorescence and flow cytometry. Results. Atorvastatin inhibited cell proliferation and DNA synthesis in both bladder cancer cell lines. This led to significant cytotoxicity as demonstrated by DNA fragmentation and induction of apoptosis. Conclusions. Atorvastatin exhibits significant antiproliferative and pro-apoptotic activity in human bladder cancer cells. This, coupled with its established clinical safety profile, provides a rationale for its use as a potential chemopreventive agent against bladder cancer.
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U2 - 10.1016/j.urology.2005.06.075
DO - 10.1016/j.urology.2005.06.075
M3 - Article
C2 - 16360444
AN - SCOPUS:29144465544
SN - 0090-4295
VL - 66
SP - 1209
EP - 1212
JO - Urology
JF - Urology
IS - 6
ER -