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Thermodynamics in Gliomas: Interactions between the Canonical WNT/Beta-Catenin Pathway and PPAR Gamma

机译:胶质瘤中的热力学:规范的WNT /β-连环蛋白途径与PPARγ之间的相互作用

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摘要

Gliomas cells are the site of numerous metabolic and thermodynamics abnormalities with an increasing entropy rate which is characteristic of irreversible processes driven by changes in Gibbs energy, heat production, intracellular acidity, membrane potential gradient, and ionic conductance. We focus our review on the opposing interactions observed in glioma between the canonical WNT/beta-catenin pathway and PPAR gamma and their metabolic and thermodynamic implications. In gliomas, WNT/beta-catenin pathway is upregulated while PPAR gamma is downregulated. Upregulation of WNT/beta-catenin signaling induces changes in key metabolic enzyme that modify their thermodynamics behavior. This leads to activation pyruvate dehydrogenase kinase 1(PDK-1) and monocarboxylate lactate transporter 1 (MCT-1). Consequently, phosphorylation of PDK-1 inhibits pyruvate dehydrogenase complex (PDH). Thus, a large part of pyruvate cannot be converted into acetyl-CoA in mitochondria and in TCA (tricarboxylic acid) cycle. This leads to aerobic glycolysis despite the availability of oxygen, named Warburg effect. Cytoplasmic pyruvate is, in major part, converted into lactate. The WNT/beta-catenin pathway induces also the transcription of genes involved in cell proliferation, cell invasiveness, nucleotide synthesis, tumor growth, and angiogenesis, such as c-Myc, cyclin D1, PDK. In addition, in gliomas cells, PPAR gamma is downregulated, leading to a decrease in insulin sensitivity and an increase in neuroinflammation. Moreover, PPAR gamma contributes to regulate some key circadian genes. Abnormalities in the regulation of circadian rhythms and dysregulation in circadian clock genes are observed in gliomas. Circadian rhythms are dissipative structures, which play a key role in far-from-equilibrium thermodynamics through their interactions with WNT/beta-catenin pathway and PPAR gamma. In gliomas, metabolism, thermodynamics, and circadian rhythms are tightly interrelated.
机译:神经胶质瘤细胞是许多代谢和热力学异常的场所,其熵率不断增加,这是由吉布斯能量,产热,细胞内酸度,膜电位梯度和离子电导率变化驱动的不可逆过程的特征。我们集中在经典的WNT /β-catenin途径和PPARγ之间的神经胶质瘤中观察到的相反相互作用及其代谢和热力学意义的审查。在神经胶质瘤中,WNT /β-catenin途径被上调而PPARγ被下调。 WNT /β-catenin信号的上调诱导关键代谢酶的改变,从而改变其热力学行为。这导致活化丙酮酸脱氢酶激酶1(PDK-1)和单羧酸酯乳酸盐转运蛋白1(MCT-1)。因此,PDK-1的磷酸化抑制了丙酮酸脱氢酶复合物(PDH)。因此,丙酮酸的大部分不能在线粒体和TCA(三羧酸)循环中转化为乙酰辅酶A。尽管有氧气,但这仍导致有氧糖酵解,称为Warburg效应。细胞质丙酮酸在很大程度上转化为乳酸。 WNT /β-catenin途径还诱导参与细胞增殖,细胞侵袭,核苷酸合成,肿瘤生长和血管生成的基因的转录,例如c-Myc,cyclin D1,PDK。另外,在神经胶质瘤细胞中,PPARγ被下调,导致胰岛素敏感性降低和神经炎症增加。此外,PPARγ有助于调节一些关键的昼夜节律基因。在神经胶质瘤中观察到昼夜节律的调节异常和昼夜节律基因的调节异常。昼夜节律是耗散结构,通过与WNT /β-catenin途径和PPARγ的相互作用,在远离平衡的热力学中发挥关键作用。在神经胶质瘤中,新陈代谢,热力学和昼夜节律紧密相关。

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