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针对肉瘤中表皮生长因子受体(EGFR)和线粒体的联合疗法的协同抑制作用。

The synergistic inhibitory effect of combining therapies targeting EGFR and mitochondria in sarcomas.

作者信息

Wang Xiaochun, Yeo Reichelle X, Hogg Philip J, Goldstein David, Crowe Philip, Dilda Pierre J, Yang Jia-Lin

机构信息

Sarcoma and Nano-oncology Group, Adult Cancer Program, Lowy Cancer Research Centre, Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, Australia.

Department of Surgery, Prince of Wales Clinical School, Faculty of Medicine, University of New South Wales, Sydney, Australia.

出版信息

Oncotarget. 2020 Jan 7;11(1):46-61. doi: 10.18632/oncotarget.27416.

Abstract

Our group previously demonstrated that sarcoma cell lines were insensitive to epidermal growth factor receptor (EGFR) inhibitor gefitinib monotherapy. PENAO, an anti-tumour metabolic compound created in our laboratory, is currently in clinical trials. Considering the positive regulation of tumour energy production by both the EGFR signalling and tumour metabolism pathways, this study aimed to investigate the effect and mechanisms of combination therapy using gefitinib and PENAO in sarcoma cell lines and . PENAO monotherapy reduced proliferation in 12 sarcoma cell lines. Combining gefitinib and PENAO resulted in synergistic inhibition in both a time- and dose-dependent manner in 3 sarcoma cell lines with less prominent monotherapy effects. Combined treatment significantly enhanced cell death and perturbed mitochondrial function. combination therapy with PENAO and gefitinib was non-toxic to mice and significantly delayed tumour growth and prolonged survival. At 20 days after treatment, tumours from the combination treated mice were significantly smaller than those from untreated and single drug treated mice. The survival curves also showed significant difference across and between groups. The combination of PENAO and gefitinib and , shows promise as a treatment pathway in this poor outcome tumour.

摘要

我们的研究小组之前证明,肉瘤细胞系对表皮生长因子受体(EGFR)抑制剂吉非替尼单药治疗不敏感。PENAO是我们实验室研发的一种抗肿瘤代谢化合物,目前正在进行临床试验。考虑到EGFR信号通路和肿瘤代谢途径对肿瘤能量产生的正向调节作用,本研究旨在探讨吉非替尼和PENAO联合治疗在肉瘤细胞系中的效果及机制。PENAO单药治疗可降低12种肉瘤细胞系的增殖。吉非替尼与PENAO联合使用对3种单药治疗效果不显著的肉瘤细胞系产生了时间和剂量依赖性的协同抑制作用。联合治疗显著增强了细胞死亡并扰乱了线粒体功能。PENAO与吉非替尼联合治疗对小鼠无毒,且显著延迟了肿瘤生长并延长了生存期。治疗20天后,联合治疗组小鼠的肿瘤明显小于未治疗组和单药治疗组小鼠的肿瘤。生存曲线也显示出各组之间存在显著差异。PENAO与吉非替尼联合使用,有望成为这种预后不良肿瘤的一种治疗途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35c8/6967775/9e4aa653072e/oncotarget-11-46-g001.jpg

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