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癌症中磷酸戊糖途径的调控

Regulation of the pentose phosphate pathway in cancer.

作者信息

Jiang Peng, Du Wenjing, Wu Mian

机构信息

School of Life Sciences, Tsinghua University, Beijing, 100084, China,

出版信息

Protein Cell. 2014;5(8):592-602. doi: 10.1007/s13238-014-0082-8. Epub 2014 Jul 12.

Abstract

Energy metabolism is significantly reprogrammed in many human cancers, and these alterations confer many advantages to cancer cells, including the promotion of biosynthesis, ATP generation, detoxification and support of rapid proliferation. The pentose phosphate pathway (PPP) is a major pathway for glucose catabolism. The PPP directs glucose flux to its oxidative branch and produces a reduced form of nicotinamide adenine dinucleotide phosphate (NADPH), an essential reductant in anabolic processes. It has become clear that the PPP plays a critical role in regulating cancer cell growth by supplying cells with not only ribose-5-phosphate but also NADPH for detoxification of intracellular reactive oxygen species, reductive biosynthesis and ribose biogenesis. Thus, alteration of the PPP contributes directly to cell proliferation, survival and senescence. Furthermore, recent studies have shown that the PPP is regulated oncogenically and/or metabolically by numerous factors, including tumor suppressors, oncoproteins and intracellular metabolites. Dysregulation of PPP flux dramatically impacts cancer growth and survival. Therefore, a better understanding of how the PPP is reprogrammed and the mechanism underlying the balance between glycolysis and PPP flux in cancer will be valuable in developing therapeutic strategies targeting this pathway.

摘要

能量代谢在许多人类癌症中发生显著重编程,这些改变赋予癌细胞许多优势,包括促进生物合成、ATP生成、解毒以及支持快速增殖。磷酸戊糖途径(PPP)是葡萄糖分解代谢的主要途径。PPP将葡萄糖通量导向其氧化分支,并产生还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH),这是合成代谢过程中必不可少的还原剂。目前已经明确,PPP通过为细胞提供不仅是5-磷酸核糖,还有用于细胞内活性氧解毒、还原生物合成和核糖生物合成的NADPH,在调节癌细胞生长中发挥关键作用。因此,PPP的改变直接影响细胞增殖、存活和衰老。此外,最近的研究表明,PPP受到多种因素的致癌性和/或代谢性调节,这些因素包括肿瘤抑制因子、癌蛋白和细胞内代谢物。PPP通量的失调会显著影响癌症的生长和存活。因此,更好地理解PPP如何重编程以及癌症中糖酵解和PPP通量之间平衡的潜在机制,对于开发针对该途径的治疗策略将具有重要价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5109/4114394/e16ec1f0a04b/13238_2014_82_Fig1_HTML.jpg

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