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XL388 在人神经胶质瘤细胞中的治疗价值。

The therapeutic value of XL388 in human glioma cells.

机构信息

Department of Neurosurgery, Rui-Jin Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, China.

Department of Stereotactic and Functional Neurosurgery, Rui-Jin Hospital, Shanghai Jiao-Tong University School of Medicine, Shanghai, China.

出版信息

Aging (Albany NY). 2020 Nov 6;12(22):22550-22563. doi: 10.18632/aging.103791.


DOI:10.18632/aging.103791
PMID:33159013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7746352/
Abstract

XL388 is a highly efficient and orally-available ATP-competitive PI3K-mTOR dual inhibitor. Its activity against glioma cells was studied here. In established and primary human glioma cells, XL388 potently inhibited cell survival and proliferation as well as cell migration, invasion and cell cycle progression. The dual inhibitor induced significant apoptosis activation in glioma cells. In A172 cells and primary human glioma cells, XL388 inhibited Akt-mTORC1/2 activation by blocking phosphorylation of Akt and S6K1. XL388-induced glioma cell death was only partially attenuated by a constitutively-active mutant Akt1. Furthermore, it was cytotoxic against Akt1-knockout A172 glioma cells. XL388 downregulated MAF bZIP transcription factor G (MAFG) and inhibited Nrf2 signaling, causing oxidative injury in glioma cells. Conversely, antioxidants, n-acetylcysteine, pyrrolidine dithiocarbamate and AGI-106, alleviated XL388-induced cytotoxicity and apoptosis in glioma cells. Oral administration of XL388 inhibited subcutaneous A172 xenograft growth in severe combined immunodeficient mice. Akt-S6K1 inhibition and MAFG downregulation were detected in XL388-treated A172 xenograft tissues. Collectively, XL388 efficiently inhibits human glioma cell growth, through Akt-mTOR-dependent and -independent mechanisms.

摘要

XL388 是一种高效、可口服的 ATP 竞争性 PI3K-mTOR 双重抑制剂。本研究探讨了其对神经胶质瘤细胞的作用。在已建立的和原代人神经胶质瘤细胞中,XL388 能强有力地抑制细胞存活、增殖以及细胞迁移、侵袭和细胞周期进程。双重抑制剂能诱导神经胶质瘤细胞发生显著的凋亡激活。在 A172 细胞和原代人神经胶质瘤细胞中,XL388 通过阻断 Akt 和 S6K1 的磷酸化来抑制 Akt-mTORC1/2 的激活。XL388 诱导的神经胶质瘤细胞死亡仅部分被 Akt1 的组成性激活突变所减弱。此外,它对 Akt1 敲除的 A172 神经胶质瘤细胞也具有细胞毒性。XL388 下调 maf 碱性亮氨酸拉链转录因子 G (MAFG) 并抑制 Nrf2 信号通路,导致神经胶质瘤细胞发生氧化损伤。相反,抗氧化剂 N-乙酰半胱氨酸、吡咯烷二硫代氨基甲酸盐和 AGI-106 能减轻神经胶质瘤细胞中 XL388 诱导的细胞毒性和凋亡。XL388 在严重联合免疫缺陷小鼠中能抑制皮下 A172 异种移植瘤的生长。在 XL388 处理的 A172 异种移植组织中检测到 Akt-S6K1 抑制和 MAFG 下调。综上,XL388 通过 Akt-mTOR 依赖性和非依赖性机制有效地抑制人神经胶质瘤细胞的生长。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/1340495403c1/aging-12-103791-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/61d4f41d0349/aging-12-103791-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/af212ed529b9/aging-12-103791-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/7f77d3938767/aging-12-103791-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/d1a957cd9795/aging-12-103791-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/1340495403c1/aging-12-103791-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/61d4f41d0349/aging-12-103791-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/af212ed529b9/aging-12-103791-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/7f77d3938767/aging-12-103791-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/d1a957cd9795/aging-12-103791-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/051c/7746352/1340495403c1/aging-12-103791-g005.jpg

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[1]
The therapeutic value of XL388 in human glioma cells.

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[4]
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[3]
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[4]
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本文引用的文献

[1]
mTOR signaling intervention by Torin1 and XL388 in the insular cortex alleviates neuropathic pain.

Neurosci Lett. 2020-1-23

[2]
Cancer statistics, 2020.

CA Cancer J Clin. 2020-1-8

[3]
Interplay of MKP-1 and Nrf2 drives tumor growth and drug resistance in non-small cell lung cancer.

Aging (Albany NY). 2019-12-6

[4]
Ninjurin2 overexpression promotes glioma cell growth.

Aging (Albany NY). 2019-12-2

[5]
Lnc-THOR silencing inhibits human glioma cell survival by activating MAGEA6-AMPK signaling.

Cell Death Dis. 2019-11-14

[6]
Promising therapeutic effect of thapsigargin nanoparticles on chronic kidney disease through the activation of Nrf2 and FoxO1.

Aging (Albany NY). 2019-11-12

[7]
Leonurine ameliorates D-galactose-induced aging in mice through activation of the Nrf2 signalling pathway.

Aging (Albany NY). 2019-9-17

[8]
Targeting Keap1 by miR-626 protects retinal pigment epithelium cells from oxidative injury by activating Nrf2 signaling.

Free Radic Biol Med. 2019-8-22

[9]
Efficiency of CellROX deep red and CellROX orange fluorescent probes in identifying reactive oxygen species in sperm samples from high and low fertility bulls.

Anim Biotechnol. 2021-2

[10]
SC79, a novel Akt activator, protects dopaminergic neuronal cells from MPP and rotenone.

Mol Cell Biochem. 2019-7-24

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