Wnt/Ca2+/NFAT signaling maintains survival of Ph+ leukemia cells upon inhibition of Bcr-Abl.

Wnt/Ca2+/NFAT signaling maintains survival of Ph+ leukemia cells upon inhibition of Bcr-Abl.
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DOI:
10.1016/j.ccr.2010.04.025
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发表时间:
2010-07-13
期刊:
影响因子:
50.3
通讯作者:
Degregori J
Degregori J
中科院分区:
医学1区
文献类型:
--
作者:
Gregory MA;Phang TL;Neviani P;Alvarez-Calderon F;Eide CA;O'Hare T;Zaberezhnyy V;Williams RT;Druker BJ;Perrotti D;Degregori J

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尽管Bcr-Abl激酶抑制剂已被证明在慢性髓性白血病(CML)的治疗中有效,但它们通常不能完全根除Bcr-Abl+白血病细胞。为了鉴定其抑制使Bcr-Abl+白血病对Bcr-Abl抑制剂杀伤敏感的基因,我们在CML细胞中用伊马替尼进行了基于RNAi的合成致死筛选。该筛选鉴定了Wnt/Ca 2 +/NFAT信号通路的许多组分。该途径的拮抗作用导致NFAT活性受损,细胞因子产生减少,对Bcr-Abl抑制的敏感性增强。此外,用环孢菌素A抑制NFAT有助于Bcr-Abl抑制剂达沙替尼消除白血病细胞,并显著改善Bcr-Abl+急性淋巴细胞白血病(ALL)小鼠模型的存活率。靶向这一途径结合Bcr-Abl抑制可以改善Bcr-Abl+白血病的治疗。
Although Bcr-Abl kinase inhibitors have proven effective in the treatment of chronic myeloid leukemia (CML), they generally fail to completely eradicate Bcr-Abl+ leukemia cells. To identify genes whose inhibition sensitizes Bcr-Abl+ leukemias to killing by Bcr-Abl inhibitors, we performed an RNAi-based synthetic lethal screen with imatinib in CML cells. This screen identified numerous components of a Wnt/Ca2+/NFAT signaling pathway. Antagonism of this pathway led to impaired NFAT activity, decreased cytokine production and enhanced sensitivity to Bcr-Abl inhibition. Furthermore, NFAT inhibition with cyclosporin A facilitated leukemia cell elimination by the Bcr-Abl inhibitor dasatinib and markedly improved survival in a mouse model of Bcr-Abl+ acute lymphoblastic leukemia (ALL). Targeting this pathway in combination with Bcr-Abl inhibition could improve treatment of Bcr-Abl+ leukemias.
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