التفاصيل البيبلوغرافية
العنوان: |
Isolation and characterization of an IGROV-1 human ovarian cancer cell line made resistant to Ecteinascidin-743 (ET-743) |
المؤلفون: |
E Erba, D Bergamaschi, L Bassano, S Ronzoni, G Di Liberti, I Muradore, S Vignati, G Faircloth, J Jimeno |
المساهمون: |
The Pennsylvania State University CiteSeerX Archives |
المصدر: |
ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/72/87/Br_J_Cancer_2000_May_27_82(10)_1732-1739.tar.gz |
المجموعة: |
CiteSeerX |
مصطلحات موضوعية: |
natural compound, Ecteinascidin-743 |
الوصف: |
Summary By exposing Igrov-1 human ovarian cancer cells to increasing concentrations of Ecteinascidin-743 (ET-743), either for a short or prolonged time, we obtained sublines resistant to ET-743 which overexpress Pgp. The most resistant clone (Igrov-1/25 ET) was evaluated for biological and pharmacological characterizations. The increased Pgp levels of Igrov-1/25 ET were not due to amplification of the mdr-1 gene but to increased mRNA levels. No increase in other multidrug resistance-related proteins such as MRP or LRP was observed in Igrov-1/25 ET. The IC 50 values of ET-743 against Igrov-1/25 ET was approximately 50 times higher than the parental cell line. Resistance was not reversed while maintaining the cell line in drug-free medium for at least 24 months. Igrov-1/25 ET was cross-resistant to Doxorubicin and VP16 while it was equally sensitive to L-PAM, MNNG, CPT and only marginally less sensitive to Cis-DDP and Oxaliplatin compared to the parental cell line. Igrov-1/25 ET exposed to Doxorubicin retained this drug much less, mainly because of a more efficient drug efflux. The cyclosporine analogue SDZ PSC-833 reversed the resistance of Igrov-1/25 ET to ET-743, without any enhancement of the drug activity against the parental Igrov-1 cell line. Igrov-1/25 ET exhibits typical features of cell lines overexpressing the mdr-1 gene and can be a potentially useful tool in selecting ET-743 non-cross-resistant analogues as well as to investigate methods to counteract resistance to this drug. © 2000 Cancer Research Campaign |
نوع الوثيقة: |
text |
وصف الملف: |
application/zip |
اللغة: |
English |
العلاقة: |
http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.275.104Test |
حقوق: |
Metadata may be used without restrictions as long as the oai identifier remains attached to it. |
رقم الانضمام: |
edsbas.54CDA70 |
قاعدة البيانات: |
BASE |