硬脂酰辅酶A去饱和酶
癌症
癌症研究
癌细胞
辅酶A
酶
脂肪酸代谢
程序性细胞死亡
脂肪酸
代谢途径
新陈代谢
生物化学
化学
生物
基因
细胞凋亡
基因表达
遗传学
还原酶
作者
Utsav Sen,Charles Coleman,Triparna Sen
标识
DOI:10.1016/j.trecan.2023.03.003
摘要
Cancer progression is a highly balanced process and is maintained by a sequence of finely tuned metabolic pathways. Stearoyl coenzyme A desaturase-1 (SCD1), the fatty enzyme that converts saturated fatty acids into monounsaturated fatty acids, is a critical modulator of the fatty acid metabolic pathway. SCD1 expression is associated with poor prognosis in several cancer types. SCD1 triggers an iron-dependent cell death called ferroptosis and elevated levels of SCD1 protect cancer cells against ferroptosis. Pharmacological inhibition of SCD1 as monotherapy and in combination with chemotherapeutic agents shows promising antitumor potential in preclinical models. In this review, we summarize the role of SCD in cancer cell progression, survival, and ferroptosis and discuss potential strategies to exploit SCD1 inhibition in future clinical trials.
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