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本文引用的文献

1
First-in-Human Phase I Study to Evaluate the Brain-Penetrant PI3K/mTOR Inhibitor GDC-0084 in Patients with Progressive or Recurrent High-Grade Glioma.在进展性或复发性高级别神经胶质瘤患者中评估具有脑穿透性的 PI3K/mTOR 抑制剂 GDC-0084 的首次人体 I 期研究。
Clin Cancer Res. 2020 Apr 15;26(8):1820-1828. doi: 10.1158/1078-0432.CCR-19-2808. Epub 2020 Jan 14.
2
Phase Ib/II single-arm trial evaluating the combination of everolimus, lapatinib and capecitabine for the treatment of HER2-positive breast cancer with brain metastases (TRIO-US B-09).Ib/II期单臂试验,评估依维莫司、拉帕替尼和卡培他滨联合治疗HER2阳性脑转移乳腺癌(TRIO-US B-09)。
Ther Adv Med Oncol. 2018 Nov 9;10:1758835918807339. doi: 10.1177/1758835918807339. eCollection 2018.
3
GDC-0084 inhibits cutaneous squamous cell carcinoma cell growth.GDC-0084 抑制皮肤鳞状细胞癌细胞生长。
Biochem Biophys Res Commun. 2018 Sep 10;503(3):1941-1948. doi: 10.1016/j.bbrc.2018.07.139. Epub 2018 Jul 30.
4
Buparlisib is a brain penetrable pan-PI3K inhibitor.布帕利西布是一种可穿透血脑屏障的全 PI3K 抑制剂。
Sci Rep. 2018 Jul 17;8(1):10784. doi: 10.1038/s41598-018-29062-w.
5
LCCC 1025: a phase II study of everolimus, trastuzumab, and vinorelbine to treat progressive HER2-positive breast cancer brain metastases.LCCC 1025:依维莫司、曲妥珠单抗和长春瑞滨治疗进展性 HER2 阳性乳腺癌脑转移的 II 期研究。
Breast Cancer Res Treat. 2018 Oct;171(3):637-648. doi: 10.1007/s10549-018-4852-5. Epub 2018 Jun 25.
6
Drug Resistance in HER2-Positive Breast Cancer Brain Metastases: Blame the Barrier or the Brain?HER2 阳性乳腺癌脑转移中的耐药性:归咎于屏障还是大脑?
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7
Inhibition of the PI3K/AKT/mTOR pathway activates autophagy and compensatory Ras/Raf/MEK/ERK signalling in prostate cancer.抑制PI3K/AKT/mTOR信号通路可激活前列腺癌中的自噬及代偿性Ras/Raf/MEK/ERK信号传导。
Oncotarget. 2017 May 23;8(34):56698-56713. doi: 10.18632/oncotarget.18082. eCollection 2017 Aug 22.
8
The brain microenvironment mediates resistance in luminal breast cancer to PI3K inhibition through HER3 activation.脑微环境通过HER3激活介导管腔型乳腺癌对PI3K抑制的抗性。
Sci Transl Med. 2017 May 24;9(391). doi: 10.1126/scitranslmed.aal4682.
9
Drug-screening and genomic analyses of HER2-positive breast cancer cell lines reveal predictors for treatment response.HER2阳性乳腺癌细胞系的药物筛选和基因组分析揭示了治疗反应的预测指标。
Breast Cancer (Dove Med Press). 2017 Mar 21;9:185-198. doi: 10.2147/BCTT.S115600. eCollection 2017.
10
Brain Distribution and Efficacy of the Brain Penetrant PI3K Inhibitor GDC-0084 in Orthotopic Mouse Models of Human Glioblastoma.脑渗透型PI3K抑制剂GDC-0084在人胶质母细胞瘤原位小鼠模型中的脑分布及疗效
Drug Metab Dispos. 2016 Dec;44(12):1881-1889. doi: 10.1124/dmd.116.071423. Epub 2016 Sep 16.

双重 PI3K/mTOR 通路抑制剂 GDC-0084 在 - 突变型乳腺癌脑转移中发挥抗肿瘤活性。

The Dual PI3K/mTOR Pathway Inhibitor GDC-0084 Achieves Antitumor Activity in -Mutant Breast Cancer Brain Metastases.

机构信息

Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

Clin Cancer Res. 2019 Jun 1;25(11):3374-3383. doi: 10.1158/1078-0432.CCR-18-3049. Epub 2019 Feb 22.

DOI:10.1158/1078-0432.CCR-18-3049
PMID:30796030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6685218/
Abstract

PURPOSE

Previous studies have shown that the PI3K/Akt/mTOR pathway is activated in up to 70% of breast cancer brain metastases, but there are no approved agents for affected patients. GDC-0084 is a brain penetrant, dual PI3K/mTOR inhibitor that has shown promising activity in a preclinical model of glioblastoma. The aim of this study was to analyze the efficacy of PI3K/mTOR blockade in breast cancer brain metastases models. The efficacy of GDC-0084 was evaluated in -mutant and wild-type breast cancer cell lines and the isogenic pairs of wild-type and mutant (H1047R/+) MCF10A cells . studies included cell viability and apoptosis assays, cell-cycle analysis, and Western blots. , the effect of GDC-0084 was investigated in breast cancer brain metastasis xenograft mouse models and assessed by bioluminescent imaging and IHC.

RESULTS

, GDC-0084 considerably decreased cell viability, induced apoptosis, and inhibited phosphorylation of Akt and p70 S6 kinase in a dose-dependent manner in -mutant breast cancer brain metastatic cell lines. In contrast, GDC-0084 led only to growth inhibition in wild-type cell lines . , treatment with GDC-0084 markedly inhibited the growth of -mutant, with accompanying signaling changes, and not wild-type brain tumors.

CONCLUSIONS

The results of this study suggest that the brain-penetrant PI3K/mTOR targeting GDC-0084 is a promising treatment option for breast cancer brain metastases with dysregulated PI3K/mTOR signaling pathway conferred by activating mutations. A national clinical trial is planned to further investigate the role of this compound in patients with brain metastases.

摘要

目的

先前的研究表明,PI3K/Akt/mTOR 通路在多达 70%的乳腺癌脑转移中被激活,但目前尚无针对此类患者的获批药物。GDC-0084 是一种具有脑穿透性的双重 PI3K/mTOR 抑制剂,在胶质母细胞瘤的临床前模型中显示出了良好的疗效。本研究旨在分析 PI3K/mTOR 阻断在乳腺癌脑转移模型中的疗效。在 -突变和 野生型乳腺癌细胞系以及 野生型和突变(H1047R/+)MCF10A 细胞的同源对中,评估了 GDC-0084 的疗效。研究包括细胞活力和凋亡检测、细胞周期分析和 Western blot。此外,还在乳腺癌脑转移异种移植小鼠模型中研究了 GDC-0084 的作用,并通过生物发光成像和免疫组化进行了评估。

结果

GDC-0084 以剂量依赖性方式显著降低了 -突变的乳腺癌脑转移细胞系的细胞活力,诱导了细胞凋亡,并抑制了 Akt 和 p70 S6 激酶的磷酸化。相比之下,GDC-0084 仅导致 野生型细胞系的生长抑制。此外,GDC-0084 的治疗显著抑制了 -突变的脑肿瘤的生长,同时伴随信号变化,但对 野生型脑肿瘤无作用。

结论

本研究结果表明,具有脑穿透性的 PI3K/mTOR 靶向药物 GDC-0084 是一种有前途的治疗选择,可用于具有失调的 PI3K/mTOR 信号通路的乳腺癌脑转移,该通路由激活 突变赋予。计划开展一项全国性临床试验,以进一步研究该化合物在脑转移患者中的作用。