TY - JOUR
T1 - Topoisomerase I-related Parameters and Camptothecin Activity in the Colon Carcinoma Cell Lines from the National Cancer Institute Anticancer Screen
AU - Goldwasser, François
AU - Bae, Insoo
AU - Valenti, Monica
AU - Torres, Keila
AU - Ponunier, Yves
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1995/5/15
Y1 - 1995/5/15
N2 - Camptothecin (CPT) derivatives are a new family of anticancer agents which are selective inhibitors of DNA topoisomerase I (topi) and have entered clinical trials with promising results. The cellular determinants for CPT activity were studied in the seven cell lines of the National Cancer Institute anticancer screen. These cell lines exhibit natural differences in sensitivity to CPT and can be divided into three groups, according to their increasing resistance: colo205, SW620, HCT116<HT29, HCC2998<HCT15, and KM12. The differential sensitivity range was approximately 17-fold between KM12 and colo205 cells. CPT uptake varied only by less than a factor of three among the cell lines. Topi mRNA, measured by Northern blotting analysis, and topi protein levels, measured by Western blotting, varied by 2-fold or less among the cell lines and were correlated neither with the CPT cytotoxicity nor the levels of deavable complexes measured by alkaline elution in the various cell lines. An overall log-linear correlation was observed between CPT-induced topl-cleavable complexes and growth inhibition, indicating the importance of deavable complex formation rather than topi levels for cell killing in this panel of cell lines. Also, some cell lines displayed marked growth inhibition differences with minimal differences in deavable complexes and S-phase fraction, suggesting that parameters downstream from the deavable complexes are also critical for CPT cytotoxicity.
AB - Camptothecin (CPT) derivatives are a new family of anticancer agents which are selective inhibitors of DNA topoisomerase I (topi) and have entered clinical trials with promising results. The cellular determinants for CPT activity were studied in the seven cell lines of the National Cancer Institute anticancer screen. These cell lines exhibit natural differences in sensitivity to CPT and can be divided into three groups, according to their increasing resistance: colo205, SW620, HCT116<HT29, HCC2998<HCT15, and KM12. The differential sensitivity range was approximately 17-fold between KM12 and colo205 cells. CPT uptake varied only by less than a factor of three among the cell lines. Topi mRNA, measured by Northern blotting analysis, and topi protein levels, measured by Western blotting, varied by 2-fold or less among the cell lines and were correlated neither with the CPT cytotoxicity nor the levels of deavable complexes measured by alkaline elution in the various cell lines. An overall log-linear correlation was observed between CPT-induced topl-cleavable complexes and growth inhibition, indicating the importance of deavable complex formation rather than topi levels for cell killing in this panel of cell lines. Also, some cell lines displayed marked growth inhibition differences with minimal differences in deavable complexes and S-phase fraction, suggesting that parameters downstream from the deavable complexes are also critical for CPT cytotoxicity.
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M3 - Article
C2 - 7743511
AN - SCOPUS:0029029436
SN - 0008-5472
VL - 55
SP - 2116
EP - 2121
JO - Cancer Research
JF - Cancer Research
IS - 10
ER -