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糖酵解在骨肉瘤中的作用。

The roles of glycolysis in osteosarcoma.

作者信息

Feng Zuxi, Ou Yanghuan, Hao Liang

机构信息

Departments of Orthopedics, Second Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

Front Pharmacol. 2022 Aug 17;13:950886. doi: 10.3389/fphar.2022.950886. eCollection 2022.

Abstract

Metabolic reprogramming is of great significance in the progression of various cancers and is critical for cancer progression, diagnosis, and treatment. Cellular metabolic pathways mainly include glycolysis, fat metabolism, glutamine decomposition, and oxidative phosphorylation. In cancer cells, reprogramming metabolic pathways is used to meet the massive energy requirement for tumorigenesis and development. Metabolisms are also altered in malignant osteosarcoma (OS) cells. Among reprogrammed metabolisms, alterations in aerobic glycolysis are key to the massive biosynthesis and energy demands of OS cells to sustain their growth and metastasis. Numerous studies have demonstrated that compared to normal cells, glycolysis in OS cells under aerobic conditions is substantially enhanced to promote malignant behaviors such as proliferation, invasion, metastasis, and drug resistance of OS. Glycolysis in OS is closely related to various oncogenes and tumor suppressor genes, and numerous signaling pathways have been reported to be involved in the regulation of glycolysis. In recent years, a vast number of inhibitors and natural products have been discovered to inhibit OS progression by targeting glycolysis-related proteins. These potential inhibitors and natural products may be ideal candidates for the treatment of osteosarcoma following hundreds of preclinical and clinical trials. In this article, we explore key pathways, glycolysis enzymes, non-coding RNAs, inhibitors, and natural products regulating aerobic glycolysis in OS cells to gain a deeper understanding of the relationship between glycolysis and the progression of OS and discover novel therapeutic approaches targeting glycolytic metabolism in OS.

摘要

代谢重编程在各种癌症的进展中具有重要意义,对癌症的进展、诊断和治疗至关重要。细胞代谢途径主要包括糖酵解、脂肪代谢、谷氨酰胺分解和氧化磷酸化。在癌细胞中,重编程代谢途径用于满足肿瘤发生和发展所需的大量能量。恶性骨肉瘤(OS)细胞的代谢也会发生改变。在重编程的代谢中,有氧糖酵解的改变是OS细胞大量生物合成和能量需求以维持其生长和转移的关键。大量研究表明,与正常细胞相比,OS细胞在有氧条件下的糖酵解显著增强,以促进OS的增殖、侵袭、转移和耐药等恶性行为。OS中的糖酵解与各种癌基因和肿瘤抑制基因密切相关,并且有许多信号通路被报道参与糖酵解的调节。近年来,已经发现大量抑制剂和天然产物通过靶向糖酵解相关蛋白来抑制OS的进展。经过数百次临床前和临床试验后,这些潜在的抑制剂和天然产物可能是治疗骨肉瘤的理想候选药物。在本文中,我们探讨调节OS细胞有氧糖酵解的关键途径、糖酵解酶、非编码RNA、抑制剂和天然产物,以更深入地了解糖酵解与OS进展之间的关系,并发现针对OS糖酵解代谢的新治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/971b/9428632/07aa86254e6c/fphar-13-950886-g001.jpg

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