Intermediary metabolism: An intricate network at the crossroads of cell fate and function

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Molecular basis of disease Pub Date : 2020-10-01 DOI:10.1016/j.bbadis.2020.165887
Leonardo M.R. Ferreira , Albert M. Li , Teresa L. Serafim , Margarida C. Sobral , M. Carmen Alpoim , Ana M. Urbano
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引用次数: 13

Abstract

Intermediary metabolism is traditionally viewed as the large, highly integrated network of reactions that provides cells with metabolic energy, reducing power and biosynthetic intermediates. The elucidation of its major pathways and molecular mechanisms of energy transduction occupied some of the brightest scientific minds for almost two centuries. When these goals were achieved, a sense that intermediary metabolism was mostly a solved problem pervaded the broader biochemical community, and the field lost its vitality. However, intermediary metabolism has recently been re-energized by several paradigm-shifting discoveries that challenged its perception as a self-contained system and re-positioned it at the crossroads of all aspects of cell function, from cell growth, proliferation and death to epigenetics and immunity. Emphasis is now increasingly placed on the involvement of metabolic dysfunction in human disease. In this review, we will navigate from the dawn of intermediary metabolism research to present day work on this ever-expanding field.

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中间代谢:一个复杂的网络在细胞命运和功能的十字路口
中间代谢传统上被认为是一个大的、高度整合的反应网络,它为细胞提供代谢能量、还原力和生物合成中间体。对能量转导的主要途径和分子机制的阐明,在近两个世纪里占据了一些最聪明的科学家的头脑。当这些目标实现时,一种认为中间代谢基本上是一个已解决的问题的感觉弥漫在更广泛的生化社区,该领域失去了活力。然而,中间代谢最近被一些范式转变的发现重新激活,这些发现挑战了它作为一个独立系统的看法,并将其重新定位于细胞功能各个方面的十字路口,从细胞生长、增殖和死亡到表观遗传学和免疫。现在越来越多的重点放在代谢功能障碍在人类疾病中的作用上。在这篇综述中,我们将从中间代谢研究的曙光到这个不断扩大的领域的今天的工作。
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来源期刊
CiteScore
12.30
自引率
0.00%
发文量
218
审稿时长
32 days
期刊介绍: BBA Molecular Basis of Disease addresses the biochemistry and molecular genetics of disease processes and models of human disease. This journal covers aspects of aging, cancer, metabolic-, neurological-, and immunological-based disease. Manuscripts focused on using animal models to elucidate biochemical and mechanistic insight in each of these conditions, are particularly encouraged. Manuscripts should emphasize the underlying mechanisms of disease pathways and provide novel contributions to the understanding and/or treatment of these disorders. Highly descriptive and method development submissions may be declined without full review. The submission of uninvited reviews to BBA - Molecular Basis of Disease is strongly discouraged, and any such uninvited review should be accompanied by a coverletter outlining the compelling reasons why the review should be considered.
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