DBeQ衍生物靶向癌细胞空泡蛋白分选4功能,抑制小鼠肿瘤生长。

IF 3.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Kevin A Fundora, Yan Zhuang, Kouta Hamamoto, Guifang Wang, Longgui Chen, Tatsuya Hattori, Xinwen Liang, Lei Bao, Venugopal Vangala, Fang Tian, Yoshinori Takahashi, Hong-Gang Wang
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引用次数: 0

摘要

液泡蛋白分选4 (VPS4)是一种aaa - atp酶,催化运输- iii解体所需的内体分选复合体,介导各种细胞膜重塑过程,包括内溶酶体膜修复和自噬体关闭。人类有2个VPS4类似物,VPS4A和VPS4B,并且在很大比例的癌症中发现了任何一个类似物的缺失,使它们依赖于剩余的类似物生存。在这项研究中,我们通过研究VPS4抑制诱导细胞死亡的机制和开发靶向VPS4功能的小分子化合物来探索VPS4抑制作为一种抗癌策略。我们发现遗传抑制VPS4可触发骨肉瘤细胞中CASP8依赖性细胞凋亡和CASP8非依赖性细胞死亡。我们合成了大约100个VPS4衍生物和相关的含AAA-ATPase valosin的蛋白抑制剂DBeQ,并使用EnzChek磷酸盐测定法和监测GFP-CHMP4B斑点形成的高含量测定法筛选了它们对VPS4 ATPase活性的抑制作用。在细胞中,先导化合物4-107引起内溶酶体损伤,破坏随后的膜修复,抑制自噬,并导致在膜上运输所需的内体分选复合物的积累。这些作用伴随着自噬体膜上CASP8的稳定,导致诱导CASP8介导的细胞凋亡。值得注意的是,4-107诱导的casp8介导的细胞死亡会因VPS4平行序列的缺失而进一步增强。此外,4-107在同基因小鼠神经母细胞瘤模型中表现出抗肿瘤活性。我们的发现为在癌症中靶向VPS4和开发VPS4抑制剂作为癌症治疗策略提供了重要的一步。意义声明:VPS4A和VPS4B是aaa - atp酶VPS4的类似物,对癌细胞存活至关重要。本研究报道了DBeQ衍生物4-107在小鼠中抑制VPS4 ATPase活性,诱导casp8介导的细胞凋亡,抑制肿瘤生长。该研究支持进一步开发VPS4A/B抑制剂作为一种有前景的抗癌治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DBeQ derivative targets vacuolar protein sorting 4 functions in cancer cells and suppresses tumor growth in mice.

Vacuolar protein sorting 4 (VPS4) is an AAA-ATPase that catalyzes the endosomal sorting complex required for transport-III disassembly, mediating various cellular membrane-remodeling processes including endolysosomal membrane repair and autophagosome closure. Humans have 2 VPS4 paralogs, VPS4A and VPS4B, and the loss of either paralog has been identified in a significant proportion of cancers, rendering them dependent on the remaining paralog for survival. In this study, we explored VPS4 inhibition as an anticancer strategy by investigating the mechanisms of VPS4 inhibition-induced cell death and developing small-molecule compounds that target VPS4 functions. We found that genetic inhibition of VPS4 triggered both caspase-8 (CASP8)-dependent apoptosis and caspase-independent cell death in osteosarcoma cells. We synthesized approximately 100 derivatives of the VPS4 and related AAA-ATPase valosin-containing protein inhibitor DBeQ and screened for their inhibitory effects on VPS4 ATPase activity using the EnzChek phosphate assay and a high-content assay monitoring GFP-CHMP4B puncta formation. In cells, the lead compound 4-107 caused endolysosomal damage, disrupted subsequent membrane repair, inhibited autophagy, and led to the accumulation of the endosomal sorting complex required for transport on membranes. These effects were accompanied by the stabilization of CASP8 on autophagosomal membranes, leading to the induction of CASP8-mediated apoptosis. Notably, the CASP8-mediated cell death induced by 4-107 was further enhanced by the loss of either VPS4 paralog. Moreover, 4-107 exhibited antitumor activity in a syngeneic mouse model of neuroblastoma. Our findings provide an important step for targeting VPS4 in cancer and developing VPS4 inhibitors as a cancer treatment strategy. SIGNIFICANCE STATEMENT: VPS4A and VPS4B, paralogs of the AAA-ATPase VPS4, are critical for cancer cell survival. This study reports that 4-107, a DBeQ derivative, inhibits VPS4 ATPase activity, induces CASP8-mediated apoptosis, and suppresses tumor growth in mice. This study supports the further development of VPS4A/B inhibitors as a promising anticancer treatment strategy.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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