Zahid M Delwar, Ake Siden, Mabel H Cruz, Juan S Yakisich
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引用次数: 0
摘要
在培养过程中,将癌细胞暴露于抗癌药物会诱导通常被认为已经死亡的细胞脱落。这些药物诱导的脱落细胞(D-IDCs)可能会给化疗带来临床问题,因为它们可能会存活下来,进入血液循环,侵入其他组织并恢复增殖,造成转移,尤其是在抗癌药物的生物利用度不足以消灭所有癌细胞的组织中。在这项研究中,我们评估了甲萘醌:正钒酸钠(M : SO)组合对 A549 肺癌细胞的抗增殖作用以及 M :SO 诱导细胞脱落的能力。此外,我们还跟踪了 M :SO 诱导的脱落细胞的转归和化学敏感性。通过使用转孔室,我们发现一部分 M :SO诱导的脱落细胞是有活力的,而且在无药培养基中重新培养时,它们能够迁移、重新附着并恢复增殖。A549 脱落耐药细胞和 M :等量的 M :SO浓度(17.5 μM : 17.5 μM)。因此,M :SO 阻止了细胞迁移。在 DBTRG.05MG 人胶质瘤细胞上也得到了类似的结果。我们的数据为进一步研究 D-IDCs 在体内的发生、其对侵袭和转移的影响及其对抗癌药物的敏感性提供了保证。
Menadione : sodium orthovanadate combination eliminates and inhibits migration of detached cancer cells.
Exposure of cancer cells to anticancer agents in cultures induces detachment of cells that are usually considered dead. These drug-induced detached cells (D-IDCs) may represent a clinical problem for chemotherapy since they may survive anoikis, enter the circulation, invade other tissues and resume proliferation, creating a metastasis, especially in tissues where the bioavailability of anticancer agents is not enough to eliminate all cancer cells. In this study we evaluated the antiproliferative effect of menadione : sodium orthovanadate (M : SO) combination on A549 lung cancer cells as well as the ability of M : SO to induce cell detachment. In addition, we followed the fate and chemosensitivity of M : SO-induced detached cells. Using transwell chambers, we found that a fraction of the M : SO-induced detached cells were viable and, furthermore, were able to migrate, re-attach, and resume proliferation when re-incubated in drug-free media. The total elimination of A549 detachment-resistant cells and M : SO-induced detached cells were successfully eliminated by equivalent M : SO concentration (17.5 μM : 17.5 μM). Thus, M : SO prevented cell migration. Similar results were obtained on DBTRG.05MG human glioma cells. Our data guarantee further studies to evaluate the in vivo occurrence of D-IDCs, their implications for invasiveness and metastasis and their sensitivity to anticancer drugs.