霉酚酸通过细胞凋亡或衰老样细胞周期阻滞克服慢性髓系白血病细胞对伊马替尼和尼洛替尼的耐药。

Leukemia Research and Treatment Pub Date : 2012-01-01 Epub Date: 2012-02-23 DOI:10.1155/2012/861301
Claire Drullion, Valérie Lagarde, Romain Gioia, Patrick Legembre, Muriel Priault, Bruno Cardinaud, Eric Lippert, François-Xavier Mahon, Jean-Max Pasquet
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引用次数: 17

摘要

我们使用对伊马替尼或尼洛替尼敏感或产生耐药的K562细胞来研究它们对霉酚酸(MPA)的反应。如膜联蛋白V标记所示,MPA诱导DNA损伤导致细胞死亡,并伴有少量凋亡(高达25%)。相比之下,在大细胞群(80%)中检测到细胞周期阻滞和衰老相关的β-半乳糖苷酶活性阳性染色。mpa诱导的细胞死亡是通过抑制自噬来实现的,这与细胞凋亡的上调有关。相反,在自噬缺陷的K562细胞中,衰老既没有减少也没有消除。对伊马替尼或尼洛替尼敏感或耐药的CML患者的原代CD34细胞对MPA有反应,但主要检测到凋亡。这些结果表明,MPA是一个有趣的工具,以克服体外和体内主要在疾病的进化阶段的耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mycophenolic Acid overcomes imatinib and nilotinib resistance of chronic myeloid leukemia cells by apoptosis or a senescent-like cell cycle arrest.

We used K562 cells sensitive or generated resistant to imatinib or nilotinib to investigate their response to mycophenolic acid (MPA). MPA induced DNA damage leading to cell death with a minor contribution of apoptosis, as revealed by annexin V labeling (up to 25%). In contrast, cell cycle arrest and positive staining for senescence-associated β-galactosidase activity were detected for a large cell population (80%). MPA-induced cell death was potentialized by the inhibition of autophagy and this is associated to the upregulation of apoptosis. In contrast, senescence was neither decreased nor abrogated in autophagy deficient K562 cells. Primary CD34 cells from CML patients sensitive or resistant to imatinib or nilotinib respond to MPA although apoptosis is mainly detected. These results show that MPA is an interesting tool to overcome resistance in vitro and in vivo mainly in the evolved phase of the disease.

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