PI3K/AKT/mTOR通路
癌症研究
体内
糖酵解
癌症
肉瘤
细胞生长
厌氧糖酵解
医学
癌细胞
化学
生物
细胞凋亡
内科学
病理
新陈代谢
生物化学
生物技术
作者
Valentina Di Gialleonardo,Hannah N. Aldeborgh,Vesselin Z. Miloushev,Kelly McBride Folkers,Kristin L. Granlund,William D. Tap,Jason S. Lewis,Wolfgang Weber,Kayvan R. Keshari
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2017-04-07
卷期号:77 (11): 3113-3120
被引量:19
标识
DOI:10.1158/0008-5472.can-16-3310
摘要
Abstract Biomarkers predicting rapalog responses in sarcomas where PI3K and mTOR are often hyperactivated could improve the suitable recruitment of responsive patients to clinical trials. PI3K/mTOR pathway activation drives energy production by regulating anaerobic glycolysis in cancer cells, suggesting a route toward a monitoring strategy. In this study, we took a multimodality approach to evaluate the phenotypic effects and metabolic changes that occur with inhibition of the PI3K/mTOR pathway. Its central role in regulating glycolysis in human sarcomas was evaluated by short- and long-term rapamycin treatment in sarcoma cell lines. We observed an overall decrease in lactate production in vitro, followed by cell growth inhibition. In vivo, we observed a similar quantitative reduction in lactate production as monitored by hyperpolarized MRI, also followed by tumor size changes. This noninvasive imaging method could distinguish reduced cell proliferation from induction of cell death. Our results illustrate the use of hyperpolarized MRI as a sensitive technique to monitor drug-induced perturbation of the PI3K/mTOR pathway in sarcomas. Cancer Res; 77(11); 3113–20. ©2017 AACR.
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