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Ouabain‐resistant non‐small‐cell lung‐cancer CELL LINE SHOWS COLLATERAL SENSITIVITY TO cis ‐diamminedichloroplatinum(II) (CDDP)
Author(s) -
Ohmori Tohru,
Nishio Kazuto,
Ohta Sei,
Kubota Naohiro,
Adachi Mitsuru,
Komiya Kazuhide,
Saijo Nagahiro
Publication year - 1994
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.2910570120
Subject(s) - ouabain , cell culture , cisplatin , cytotoxicity , chemistry , cell , atpase , microbiology and biotechnology , biology , endocrinology , medicine , biochemistry , in vitro , enzyme , sodium , chemotherapy , genetics , organic chemistry
We have reported that the cellular uptake of cis‐diamminedi‐chloroplatinum(11) (CDDP) was inhibited by an Na + ,K + ‐adenosine triphosphatase (ATPase) inhibitor, ouabain, in a human non‐small‐cell lung‐cancer cell line, PC‐14, but not in its CDDP‐resistant cell line, PC‐14/CDDP. [ 3 H]Ouabain binding of PC‐14/CDDP was about 50% lower than that of PC‐14. Accordingly, we speculated that a decrease in Na + ,K + ‐ATPase activity in PC‐14/CDDP might contribute to the decrease in cellular CDDP accumulation. To clarify the relationship between the activity or expression of Na + ,K + ‐ATPase and cellular CDDP accumulation, we established an ouabain‐resistant non‐small‐cell lung‐cancer cell line (PC‐14/OB300), which showed 1.9‐fold resistance to the cytotoxicity of ouabain. Interestingly, this cell line was 4.2‐fold more sensitive to CDDP than PC‐14. The accumulation of CDDP in PC‐14/OB300 was increased to 2.7‐fold that in PC‐14. This elevation of CDDP accumulation was not considered to be caused by increased passive diffusion, because the accumulation of CDDP in PC‐14/OB300 was also inhibited by ouabain compared to PC‐14. As one of the indices of Na + .K + ‐ATPase activity, we determined cellular 86 Rb + influx rates. The 86 Rb + influx rate was 1.5‐fold higher in PC‐14/OB300 and fell to 0.7‐fold in PC‐14/CDDP compared with PC‐14. The mRNA expression of Na + ,K + ‐ATPase was increased in PC‐14/OB300 and decreased in PC‐ 14/CDDP. There was no difference in cellular [ 3 H]ouabain binding between PC‐14/OB300 and PC‐14. It is passible that Na + ,K + ‐ATPase of PC‐14/OB300 has a different affinity for ouabain from that of PC‐14. Our results suggest that the enzyme activity or the level of expression of Na + ,K + ‐ATPase may contribute to the cellular uptake of CDDP and determine the sensitivity to CDDP. © Wiley‐Liss, Inc.