Woodward Julia K L, Neville-Webbe Helen L, Coleman Robert E, Holen Ingunn
Academic Unit of Clinical Oncology, Genomic Medicine, Medical School, University of Sheffield, UK.
Anticancer Drugs. 2005 Sep;16(8):845-54. doi: 10.1097/01.cad.0000175582.01446.6f.
The bisphosphonate zoledronic acid and the cytotoxic drug doxorubicin induce synergistic levels of apoptosis in breast cancer cells. As zoledronic acid and doxorubicin have been shown to reduce cell invasion and migration, we have investigated if these drugs also act synergistically on breast cancer invasion in vitro. MCF7 cells were treated with 0.05 microM doxorubicin/4 h followed by 1 or 10 microM zoledronic acid/24 h (or the reverse sequence). To study invasion, MCF7 cells were either grown on Transwell membranes coated with Matrigel or in a 24-well plate. Cells were treated sequentially using the above drug combinations, prior to starting the invasion assays for 48 h. Cell growth and death were also assessed under the same conditions. We found that invasion of MCF7 cells treated with zoledronic acid and doxorubicin was significantly reduced when compared with control, but the effect was dependent on drug sequence. At 1 microM, zoledronic acid significantly reduced invasion only if cells were pre-treated with doxorubicin, but cell growth was unaffected. For 10 microM zoledronic acid, invasion was reduced when administered before or after the doxorubicin, but this dose of zoledronic acid caused a significant reduction in MCF7 growth. Apoptosis was not induced by any of the drug doses and combinations. We conclude that pre-treatment with 0.05 microM doxorubicin followed by 1 microM zoledronic acid reduces invasion when cells were grown on Matrigel. For 10 microM zoledronic acid, pre- or post-doxorubicin also reduces invasion, but for this combination inhibition of cell growth may contribute to the reduction in invasion observed.
双膦酸盐唑来膦酸和细胞毒性药物阿霉素可诱导乳腺癌细胞产生协同水平的细胞凋亡。由于已证明唑来膦酸和阿霉素可减少细胞侵袭和迁移,我们研究了这些药物在体外对乳腺癌侵袭是否也具有协同作用。MCF7细胞先用0.05微摩尔/升阿霉素处理4小时,然后用1或10微摩尔/升唑来膦酸处理24小时(或相反顺序)。为了研究侵袭,MCF7细胞要么生长在涂有基质胶的Transwell膜上,要么生长在24孔板中。在开始48小时的侵袭试验之前,使用上述药物组合依次处理细胞。在相同条件下还评估了细胞生长和死亡情况。我们发现,与对照组相比,用唑来膦酸和阿霉素处理的MCF7细胞的侵袭明显减少,但效果取决于药物顺序。在1微摩尔/升时,只有当细胞先用阿霉素预处理时,唑来膦酸才会显著降低侵袭,但细胞生长不受影响。对于10微摩尔/升的唑来膦酸,在阿霉素之前或之后给药时侵袭都会减少,但该剂量的唑来膦酸会导致MCF7生长显著降低。任何药物剂量和组合均未诱导细胞凋亡。我们得出结论,当细胞生长在基质胶上时,先用0.05微摩尔/升阿霉素预处理,然后用1微摩尔/升唑来膦酸处理可减少侵袭。对于10微摩尔/升的唑来膦酸,在阿霉素之前或之后使用也可减少侵袭,但对于这种组合,细胞生长的抑制可能导致观察到的侵袭减少。