脂质代谢
内分泌学
脂肪酸
内科学
新陈代谢
下调和上调
脂肪酸合成
代谢物
饱和脂肪酸
细胞生长
脂肪酸代谢
亚油酸
化学
生物
生物化学
医学
基因
作者
Evan C. Lien,Anna M. Westermark,Yin Zhang,Chen Yuan,Zhaoqi Li,Allison N. Lau,Kiera M. Sapp,Brian M. Wolpin,Matthew G. Vander Heiden
出处
期刊:Nature
[Springer Nature]
日期:2021-10-20
卷期号:599 (7884): 302-307
被引量:160
标识
DOI:10.1038/s41586-021-04049-2
摘要
Dietary interventions can change metabolite levels in the tumour microenvironment, which might then affect cancer cell metabolism to alter tumour growth1-5. Although caloric restriction (CR) and a ketogenic diet (KD) are often thought to limit tumour progression by lowering blood glucose and insulin levels6-8, we found that only CR inhibits the growth of select tumour allografts in mice, suggesting that other mechanisms contribute to tumour growth inhibition. A change in nutrient availability observed with CR, but not with KD, is lower lipid levels in the plasma and tumours. Upregulation of stearoyl-CoA desaturase (SCD), which synthesises monounsaturated fatty acids, is required for cancer cells to proliferate in a lipid-depleted environment, and CR also impairs tumour SCD activity to cause an imbalance between unsaturated and saturated fatty acids to slow tumour growth. Enforcing cancer cell SCD expression or raising circulating lipid levels through a higher-fat CR diet confers resistance to the effects of CR. By contrast, although KD also impairs tumour SCD activity, KD-driven increases in lipid availability maintain the unsaturated to saturated fatty acid ratios in tumours, and changing the KD fat composition to increase tumour saturated fatty acid levels cooperates with decreased tumour SCD activity to slow tumour growth. These data suggest that diet-induced mismatches between tumour fatty acid desaturation activity and the availability of specific fatty acid species determine whether low glycaemic diets impair tumour growth.
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