Human Telomerase Reverse Transcriptase (hTERT): A Target Molecule for the Treatment of Cisplatin-resistant Tumors

Yuk Pheel Park, Kwang Dong Kim, Seong Ho Kang, Do-Young Yoon, Joo Won Park, Jong Wan Kim, Hee Gu Lee
2008 The Korean Journal of Laboratory Medicine  
Cisplatin (cis-diammine-dichloro-platinum II ) is one of the most effective chemotherapeutic agents and is widely used for the treatment of malignant tumors, including those found in the testis, head, neck, esophagus, lung, ovaries, 430 Background : Human telomerase reverse transcriptase (hTERT) is a catalytic enzyme that is required for telomerase activity (TA) and cancer progression. Telomerase inhibition or inactivation increases cellular sensitivity to UV irradiation, DNA-damaging agents,
more » ... e tyrosine kinase inhibitor, imatinib, and pharmacological inhibitors, such as BIBR1532. hTERT is associated with apoptosis. Some patients show drug-resistance during anti-cancer drug treatment and the cancer cell acquire anti-apoptotic mechanism. Therefore, we attempted to study correlation between hTERT and drug-resistance. Methods : To study the correlation between protein level and activity of hTERT and drug-resistance, Western blotting and telomerase repeat amplification protocol (TRAP) assays were performed. To investigate whether hTERT contributes to drug resistance in tumor cells, we transiently decreased hTERT levels using small interfering RNA (siRNA) in T24/R2 cells. Results : hTERT knockdown increased Bax translocation into the mitochondria and cytochrome C release into the cytosol. Caspase inhibitors, especially Z-VAD-FMK, rescued this phenomenon, suggesting that the stability or expression of hTERT might be regulated by caspase activity. Conclusions : These data suggest that hTERT might be a target molecule for drug-resistant tumor therapy. (Korean J Lab Med 2008;28:430-7)
doi:10.3343/kjlm.2008.28.6.430 pmid:19127107 fatcat:2vapuh63l5c5xh23n4ai475shm