Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China.
State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Key Laboratory of Plant Resources and Chemistry in Arid Regions, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, China.
Phytother Res. 2023 May;37(5):2036-2050. doi: 10.1002/ptr.7735. Epub 2023 Feb 7.
Gastrointestinal cancer (GIC), including gastric cancer and colorectal cancer, is a common malignant tumor originating from gastrointestinal epithelial cells. Although the pathogenesis of GIC remains unclear, aberrant lipid metabolism has emerged as a hallmark of cancer. Several enzymes, proteins, and transcription factors are involved in lipid metabolism reprogramming in GIC, and their abnormal expression can promote lipid synthesis and accumulation of lipid droplets through numerous mechanisms, thereby affecting the growth, proliferation, and metastasis of GIC cells. Studies show that some natural compounds, including flavonoids, alkaloids, and saponins, can inhibit the de novo synthesis of lipids in GIC, reduce the level of lipid accumulation, and subsequently, inhibit the occurrence and development of GIC by regulating Sterol regulatory element-binding protein 1 (SREBP-1), adenosine monophosphate-activated protein kinase (AMPK), 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR), phosphatidylinositol-3-kinase/Akt and the mammalian target of rapamycin PI3K/Akt/mTOR, amongst other targets and pathways. Therefore, targeting tumor lipid metabolism is the focus of anti-gastrointestinal tumor therapy. Although most natural products require further high-quality studies to firmly establish their clinical efficacy, we review the potential of natural products in the treatment of GIC and summarize the application prospect of lipid metabolism as a new target for the treatment of GIC, hoping to provide a reference for drug development for gastrointestinal tumors.
胃肠道癌症(GIC),包括胃癌和结直肠癌,是一种常见的源自胃肠道上皮细胞的恶性肿瘤。尽管 GIC 的发病机制尚不清楚,但异常的脂质代谢已成为癌症的标志。几种酶、蛋白质和转录因子参与 GIC 中的脂质代谢重编程,它们的异常表达可以通过多种机制促进脂质合成和脂质滴的积累,从而影响 GIC 细胞的生长、增殖和转移。研究表明,一些天然化合物,包括类黄酮、生物碱和皂苷,可抑制 GIC 中脂质的从头合成,减少脂质积累水平,进而通过调节固醇调节元件结合蛋白 1(SREBP-1)、腺苷单磷酸激活蛋白激酶(AMPK)、3-羟-3-甲基戊二酰辅酶 A 还原酶(HMGCR)、磷酸肌醇-3-激酶/蛋白激酶 B(PI3K/Akt)和雷帕霉素哺乳动物靶蛋白(mTOR)等靶点和途径,抑制 GIC 的发生和发展。因此,针对肿瘤脂质代谢是抗胃肠道肿瘤治疗的重点。尽管大多数天然产物需要进一步的高质量研究来确定其临床疗效,但我们综述了天然产物在治疗 GIC 中的潜力,并总结了脂质代谢作为治疗 GIC 的新靶点的应用前景,希望为胃肠道肿瘤的药物开发提供参考。