Cancer Center, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Neurology, Heidelberg University Hospital, Heidelberg, Germany.
Clin Cancer Res. 2019 Jun 1;25(11):3374-3383. doi: 10.1158/1078-0432.CCR-18-3049. Epub 2019 Feb 22.
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.
, 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.
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.
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。
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。
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。