Abstract
In a previous study, we established camptothecin (CPT)-resistant cell lines, A549/CPT and HT-29/CPT, from human lung cancer A549 and human colon cancer HT-29. A549/CPT was shown to express similar amounts of DNA topoisomerase I (topo I) as the parental line, and HT-29/CPT was shown to express lower amounts of topo I than its parental line. DNA topoisomerases I and II are known to be functionally related. In the present study, the possible alterations in topo II expression were examined in these human CPT-resistant lines. In A549/CPT and HT-29/CPT, the cellular contents of topo II and its mRNA were elevated over that seen in each parental line. Nuclear extracts from A549/CPT and HT-29/CPT showed higher topo II activity than those from the corresponding parental lines when the same amounts of nuclear protein were used. Topo II was partially purified from HT-29 and HT-29/CPT by hydroxylapatite column chromatography, and the enzyme activities were compared. HT-29/CPT showed higher topo II activity in the hydroxylapatite column-eluted fractions that HT-29. These results indicate the possible activation of topo II expression in the CPT-resistant cell lines.
Footnotes
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↵1 Supported in part by grants from the Ministry of Education, Science and Culture, Japan; from the Ministry of Health and Welfare, Japan; and from the Foundation for Promotion of Cancer Research, Japan.
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↵2 To whom requests for reprints should be addressed, at Cancer Chemotherapy Center, Japanese Foundation for Cancer Research, Kami-Ikebukuro 1-37-1, Toshima-ku, Tokyo 170, Japan.
- Received July 2, 1990.
- Accepted September 18, 1990.
- ©1990 American Association for Cancer Research.