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Cited 5 time in webofscience Cited 6 time in scopus
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Adenovirus-mediated antisense telomerase with cisplatin increased the susceptibility of cisplatin resistant ovarian cancer cell line

Authors
Kim, DSSong, JSLee, KWKim, MHKim, KTKim, HKim, YT
Issue Date
Oct-2002
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
telomerase; ovarian cancer; adenovirus; cisplatin; targeted cancer gene therapy
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.12, no.5, pp 711 - 715
Pages
5
Indexed
SCIE
SCOPUS
KCI
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
12
Number
5
Start Page
711
End Page
715
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2020.sw.kumedicine/36945
ISSN
1017-7825
1738-8872
Abstract
Telomerase adds telomeric repeats to chromosomal ends and is known to play an important role in carcinogenesis through cellular immortalization. Since telomerase is an essential pathogenomic factor in malignant tumors, inhibiting telomerase activity is thought to be possible to make telomerase positive tumors more sensitive to cisplatin treatment, which is effective in ovarian cancers, but clinical success is limited by chemo-resistance. In the present study, cisplatin-sensitive ovarian cancer cell line A2780 and cisplatin-resistant A2780/cp70 cell line were infected with antisense telomerase adenovirus Ad-OA. It was found that the Ad-OA suppressed ovarian cancer cell growth and this effect was mainly due to the induction of caspase-dependent apoptosis. Next, we infected the cisplatin resistant ovarian cancer cell line A2780/cp70 with Ad-OA and cisplatin concurrently. Interestingly, cisplatin treatment with Ad-OA was more effective to cisplatin-induced cell death in A2780/cp70 cells compared to cisplatin or the vector group only. These data suggest that cisplatin treatment with Ad-OA may be a new chemo-sensitizer for cisplatin resistant ovarian cancer.
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