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通过……调节信号通路促进肝细胞癌中的脂质代谢。

promotes lipid metabolism in hepatocellular carcinoma by regulating the signaling pathway through .

作者信息

Sun Yaocheng, Shen Ying, Yan Yongmin, Luo Wei, Liu Chuanlei, Tang Jianjun

机构信息

Department of General Surgery, The Wujin Clinical College of Xuzhou Medical University Changzhou 213017, Jiangsu, China.

Department of General Surgery, Wujin Hospital Affiliated with Jiangsu University Changzhou 213017, Jiangsu, China.

出版信息

Am J Transl Res. 2025 Apr 15;17(4):2527-2540. doi: 10.62347/ZTGP5030. eCollection 2025.

DOI:10.62347/ZTGP5030
PMID:40385002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12082496/
Abstract

OBJECTIVES

Cancer cells exhibit altered metabolic profiles. Glutaminase 1 (), a key enzyme in cancer cells, promoting glutamine catabolism to glutamate and ammonia, is strongly associated with various human malignancies.

METHODS

promotes lipid accumulation and cell proliferation by upregulating the expression of sterol regulatory element-binding protein 1 () and SREBP cleavage-activating protein (). Mechanistically, promotes lipid metabolism in HCC cells through the activation of the pathway.

RESULTS

's role in lipid metabolism in hepatocellular carcinoma (HCC) remains unexplored. Our findings indicate that is not only significantly overexpressed in HCC but also negatively correlates with clinical prognosis. Further investigation revealed that drives lipid accumulation and de novo fatty acid synthesis in HCC.

CONCLUSIONS

Our study suggests that mediates to drive lipid metabolism in HCC via the phosphatidylinositol-3-kinase/protein kinase B/mammalian target of rapamycin complex 1 () signaling pathway, thus we present as a potential biomarker and therapeutic target for HCC.

摘要

目的

癌细胞表现出代谢谱的改变。谷氨酰胺酶1()是癌细胞中的一种关键酶,可促进谷氨酰胺分解为谷氨酸和氨,与多种人类恶性肿瘤密切相关。

方法

通过上调固醇调节元件结合蛋白1()和SREBP裂解激活蛋白()的表达促进脂质积累和细胞增殖。机制上,通过激活途径促进肝癌细胞的脂质代谢。

结果

在肝细胞癌(HCC)脂质代谢中的作用仍未被探索。我们的研究结果表明,不仅在肝癌中显著过表达,而且与临床预后呈负相关。进一步研究发现,在肝癌中驱动脂质积累和从头脂肪酸合成。

结论

我们的研究表明,通过磷脂酰肌醇-3-激酶/蛋白激酶B/雷帕霉素复合物1()信号通路介导驱动肝癌中的脂质代谢,因此我们提出作为肝癌的潜在生物标志物和治疗靶点。

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本文引用的文献

1
Targeting SREBP-1-Mediated Lipogenesis as Potential Strategies for Cancer.靶向SREBP-1介导的脂肪生成作为癌症的潜在治疗策略
Front Oncol. 2022 Jul 14;12:952371. doi: 10.3389/fonc.2022.952371. eCollection 2022.
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Lipid metabolism in tumor microenvironment: novel therapeutic targets.肿瘤微环境中的脂质代谢:新型治疗靶点
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ACLY inhibitors induce apoptosis and potentiate cytotoxic effects of sorafenib in thyroid cancer cells.ACLY 抑制剂诱导甲状腺癌细胞凋亡,并增强索拉非尼的细胞毒作用。
Endocrine. 2022 Oct;78(1):85-94. doi: 10.1007/s12020-022-03124-6. Epub 2022 Jun 27.
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Metabolic Reprogramming in Cancer Cells: Emerging Molecular Mechanisms and Novel Therapeutic Approaches.癌细胞中的代谢重编程:新兴分子机制与新型治疗方法
Pharmaceutics. 2022 Jun 19;14(6):1303. doi: 10.3390/pharmaceutics14061303.
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Metabolic reprogramming: a bridge between aging and tumorigenesis.代谢重编程:衰老与肿瘤发生之间的桥梁。
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Inhibiting SCAP/SREBP exacerbates liver injury and carcinogenesis in murine nonalcoholic steatohepatitis.抑制 SCAP/SREBP 加剧了小鼠非酒精性脂肪性肝炎的肝损伤和癌变。
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Risk factors for HCC in contemporary cohorts of patients with cirrhosis.肝硬化患者当代队列中 HCC 的风险因素。
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The Neglected Liaison: Targeting Cancer Cell Metabolic Reprogramming Modifies the Composition of Non-Malignant Populations of the Tumor Microenvironment.被忽视的联系:靶向癌细胞代谢重编程可改变肿瘤微环境中非恶性细胞群的组成。
Cancers (Basel). 2021 Oct 29;13(21):5447. doi: 10.3390/cancers13215447.
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SREBP-1c and lipogenesis in the liver: an update1.SREBP-1c 与肝脏中的脂肪生成:最新进展综述1。
Biochem J. 2021 Oct 29;478(20):3723-3739. doi: 10.1042/BCJ20210071.
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Hypoxia, Metabolic Reprogramming, and Drug Resistance in Liver Cancer.肝癌中的缺氧、代谢重编程与耐药性
Cells. 2021 Jul 6;10(7):1715. doi: 10.3390/cells10071715.