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Novel cellular determinants for reversal of multidrug resistance in cells expressing P170-glycoprotein
Journal article   Open access   Peer reviewed

Novel cellular determinants for reversal of multidrug resistance in cells expressing P170-glycoprotein

Ming-biao Yin, Bin Guo, Wieland Voigt, Udo Vanhoefer, John F Gibbs, Basil S Skenderis, Cheryl Frank, Carol Wrzosek and Youcef M Rustum
Biochimica et biophysica acta. Molecular cell research, Vol.1401(3), pp.265-276
1998
DOI: 10.1016/S0167-4889(97)00137-7
PMID: 9540817
url
https://doi.org/10.1016/s0167-4889(97)00137-7View
Published (Version of record) Open Access

Abstract

The newly synthesized calcium channel blocker, Ro44-5912, significantly potentiates doxorubicin (Dox)-induced cytotoxicity at non-cytotoxic concentrations in Dox-resistant human ovarian cell line, A2780/DX5, overexpressing P170-glycoprotein (Pgp). Induction of DNA single- and double-strand breaks (ssbs and dsbs) was measured using alkaline elution and constant-field gel electrophoresis (CFGE) assays. The results indicate that potentiation of the cytotoxicity of Dox by Ro44-5912 was accompanied by significant increases in both, Dox-induced DNA ssbs and dsbs in the resistant cells. Pulsed-field gel electrophoresis (PFGE) analysis showed that Dox induced DNA fragments in the 50–800 kilobase (kb) and 0.8–5.7 megabase (Mb) ranges. The majority of the newly synthesized DNA fragments were in the 50–800 kb range. Ro44-5912 treatment resulted in significant potentiation of DNA fragmentation in the 50–800 kb range with a minor increase in 0.8–5.7 Mb DNA fragments, suggesting that the modulator functions by potentiating nascent DNA fragmentation in the resistant cells. Exposure to Dox with Ro44-5912 was associated with a prolonged blockage of cells in the S-phase. In contrast, exposure to Dox alone resulted in temporary blockage of cells in G 2/M phase (∼24 h) followed by restoration of cell proliferation and normal DNA histograms at 48 h after 2 h drug exposure. Incorporation of BrdUrd by flow cytometric analysis was inhibited by Dox in the presence of Ro44-5912, showing that there is a block of DNA replication. An increased damage in newly synthesized DNA could concur with a blocked DNA replication. Moreover, slowing progression through the S-phase in cells exposed to Dox in combination with Ro44-5912 is accompanied by increased sensitivity of Dox poisons, indicating a correlation of specific S-phase perturbation with the reversal of Dox resistance by Ro44-5912 in cells expressing Pgp. The results suggest that drug-induced augmentation of nascent DNA fragmentation and specific cell-cycle perturbation are potentially important molecular determinants for reversal of multidrug resistance in addition to restoration of intracellular drug retention.
 Cell-cycle perturbation DNA fragmentation Doxorubicin Multidrug resistance Ro44-5912

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