GZ17-6.02 与蛋白酶体抑制剂相互作用,可杀死多发性骨髓瘤细胞。

Q2 Medicine
Laurence Booth, Jane L Roberts, Cameron West, Paul Dent
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引用次数: 0

摘要

GZ17-6.02是一种合成化合物,含有异香兰素、禾本科植物碱和姜黄素,已在实体瘤患者中进行了I期评估(NCT03775525),建议的2期剂量(RP2D)为375毫克,每日2次。与之前在实体瘤细胞类型中观察到的效果相比,GZ17-6.02 作为一种单药杀死多发性骨髓瘤细胞的效果更好。GZ17-6.02与蛋白酶体抑制剂的相互作用杀死骨髓瘤细胞的效果超过了相加的效果,而单独使用GZ17-6.02杀死对抑制剂耐药的细胞的效果也类似。GZ17-6.02 和硼替佐米的药物组合激活了 ATM、AMPK 和 PERK,并使 ULK1、mTORC1、eIF2α、NFκB 和 Hippo 通路失活。两者的结合增加了 ATG13 S318 磷酸化和 Beclin1、ATG5、BAK 和 BIM 的表达,并降低了 BCL-XL 和 MCL1 的水平。GZ17-6.02与硼替佐米相互作用,增强自噬体的形成和自噬通量,而敲除ATM、AMPKα、ULK1、Beclin1或ATG5会显著降低自噬和肿瘤细胞杀伤力。敲除 BAK 和 BIM 能明显降低肿瘤细胞的杀伤力。HDACs1/2/3的表达明显减少,超出了之前在实体瘤细胞中观察到的水平,并且需要自噬。这与组蛋白 H3 的乙酰化和甲基化增加有关。联合敲除 HDACs1/2/3 可激活 ATM 和 AMPK,并导致 ULK1、mTORC1、NFκB 和 Hippo 通路失活。敲除 HDAC 还能增强 ATG13 磷酸化、提高 BAK 水平并降低 BCL-XL 水平。总之,我们目前的研究支持对多发性骨髓瘤细胞进行更多的体内研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GZ17-6.02 interacts with proteasome inhibitors to kill multiple myeloma cells.

GZ17-6.02, a synthetically manufactured compound containing isovanillin, harmine and curcumin, has undergone phase I evaluation in patients with solid tumors (NCT03775525) with a recommended phase 2 dose (RP2D) of 375 mg PO BID. GZ17-6.02 was more efficacious as a single agent at killing multiple myeloma cells than had previously been observed in solid tumor cell types. GZ17-6.02 interacted with proteasome inhibitors in a greater than additive fashion to kill myeloma cells and alone it killed inhibitor-resistant cells to a similar extent. The drug combination of GZ17-6.02 and bortezomib activated ATM, the AMPK and PERK and inactivated ULK1, mTORC1, eIF2α, NFκB and the Hippo pathway. The combination increased ATG13 S318 phosphorylation and the expression of Beclin1, ATG5, BAK and BIM, and reduced the levels of BCL-XL and MCL1. GZ17-6.02 interacted with bortezomib to enhance autophagosome formation and autophagic flux, and knock down of ATM, AMPKα, ULK1, Beclin1 or ATG5 significantly reduced both autophagy and tumor cell killing. Knock down of BAK and BIM significantly reduced tumor cell killing. The expression of HDACs1/2/3 was significantly reduced beyond that previously observed in solid tumor cells and required autophagy. This was associated with increased acetylation and methylation of histone H3. Combined knock down of HDACs1/2/3 caused activation of ATM and the AMPK and caused inactivation of ULK1, mTORC1, NFκB and the Hippo pathway. HDAC knock down also enhanced ATG13 phosphorylation, increased BAK levels and reduced those of BCL-XL. Collectively, our present studies support performing additional in vivo studies with multiple myeloma cells.

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来源期刊
Oncotarget
Oncotarget Oncogenes-CELL BIOLOGY
CiteScore
6.60
自引率
0.00%
发文量
129
审稿时长
1.5 months
期刊介绍: Information not localized
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