TY - JOUR
T1 - The activity profile of the hexacyclic camptothecin derivative DX-8951f in experimental human colon cancer and ovarian cancer
AU - Van Hattum, Annemarie H.
AU - Pinedo, Herbert M.
AU - Schlüper, Hennie M M
AU - Erkelens, Caroline A M
AU - Tohgo, Akiko
AU - Boven, Epie
PY - 2002/10/15
Y1 - 2002/10/15
N2 - DX-8951f or exatecan mesylate ((1S,9S)-1-amino-9-ethyl-5-fluoro-2,3-dihydro-9-hydroxy-4-methyl-1H,12H- benzo[de]pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-10-13(9H, 15H)-dione methanesulfonate dihydrate), is a new water-soluble derivative of camptothecin. We determined the activity of DX-8951f in experimental human colon cancer and ovarian cancer, being tumor types sensitive to camptothecins. With the use of the MTT assay, DX-8951f was more potent than SN-38 in four out of five human colon cancer cell lines and three out of four human ovarian cancer cell lines (P <0.05). DX-8951f was considerably more potent than topotecan in all cell lines tested (P <0.05). Prolonged exposure to DX-8951f resulted in a greater increase in inhibition of cell proliferation as compared to that obtained with SN-38 or topotecan (P <0.05). Overexpression of Pgp, MRP1, and LRP did not affect the in vitro activity of DX-8951f. DX-8951f administered daily × 5 or weekly × 2 resulted in growth inhibition 50% growth inhibition was observed at both schedules. In the OVCAR-3 human ovarian cancer model, DX-8951f showed considerably greater activity than topotecan (P <0.01). DX-8951f combined with cisplatin or paclitaxel did not indicate the presence of a pharmacological interaction. In OVCAR-3 xenografts the combination was clearly more effective than DX-8951f alone, as the number of complete remissions increased substantially. In conclusion, this study shows that DX-8951f is highly potent in vitro and highly effective in experimental human ovarian cancer in vivo. Prolonged exposure to DX-8951f in vitro greatly increased the antiproliferative effects, which may be a rationale for testing a continuous infusion schedule in the clinic. Addition of cisplatin or paclitaxel improved the in vivo antitumor effects of DX-8951f.
AB - DX-8951f or exatecan mesylate ((1S,9S)-1-amino-9-ethyl-5-fluoro-2,3-dihydro-9-hydroxy-4-methyl-1H,12H- benzo[de]pyrano[3′,4′:6,7]indolizino[1,2-b]quinoline-10-13(9H, 15H)-dione methanesulfonate dihydrate), is a new water-soluble derivative of camptothecin. We determined the activity of DX-8951f in experimental human colon cancer and ovarian cancer, being tumor types sensitive to camptothecins. With the use of the MTT assay, DX-8951f was more potent than SN-38 in four out of five human colon cancer cell lines and three out of four human ovarian cancer cell lines (P <0.05). DX-8951f was considerably more potent than topotecan in all cell lines tested (P <0.05). Prolonged exposure to DX-8951f resulted in a greater increase in inhibition of cell proliferation as compared to that obtained with SN-38 or topotecan (P <0.05). Overexpression of Pgp, MRP1, and LRP did not affect the in vitro activity of DX-8951f. DX-8951f administered daily × 5 or weekly × 2 resulted in growth inhibition 50% growth inhibition was observed at both schedules. In the OVCAR-3 human ovarian cancer model, DX-8951f showed considerably greater activity than topotecan (P <0.01). DX-8951f combined with cisplatin or paclitaxel did not indicate the presence of a pharmacological interaction. In OVCAR-3 xenografts the combination was clearly more effective than DX-8951f alone, as the number of complete remissions increased substantially. In conclusion, this study shows that DX-8951f is highly potent in vitro and highly effective in experimental human ovarian cancer in vivo. Prolonged exposure to DX-8951f in vitro greatly increased the antiproliferative effects, which may be a rationale for testing a continuous infusion schedule in the clinic. Addition of cisplatin or paclitaxel improved the in vivo antitumor effects of DX-8951f.
KW - Colon cancer
KW - DX-8951f
KW - Human tumor xenografts
KW - Ovarian cancer
KW - Topoisomerase I inhibitor
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UR - http://www.scopus.com/inward/citedby.url?scp=0037107555&partnerID=8YFLogxK
U2 - 10.1016/S0006-2952(02)01297-2
DO - 10.1016/S0006-2952(02)01297-2
M3 - Article
C2 - 12234607
AN - SCOPUS:0037107555
SN - 0006-2952
VL - 64
SP - 1267
EP - 1277
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 8
ER -