Literature DB >> 28356004

Post-Transcriptional and Post-translational Regulation of Central Carbon Metabolic Enzymes in Cancer.

Yunqian Wang1, Yingxuan Chen1, Jingyuan Fang1.   

Abstract

Malignant transformation of cells requires specific adaptations of cellular metabolism to support growth and survival. Alterations in cancer central carbon metabolism including aerobic glycolysis, elevated glutaminolysis, dysregulated tricarboxylic acid cycle and pentose phosphate pathway, facilitate cancer development by maintaining viability and building new biomass. Although a variety of oncogenes or tumor suppressors contribute to these rewiring, accumulating evidence suggests that both post-transcriptional and post-translational modifications (PTMs) also orchestrate the tightly controlled regulation of cancer metabolic adaptations, broadening the biological mechanisms of cancer metabolic reprogramming. Micro RNA, one kind of posttranscriptional modification, mediates transcriptional silencing of various metabolic enzymes. Additional, different kinds of PTMs play important roles in cancer metabolic rewiring by affecting the function, interaction or stability of target proteins. We survey recent studies demonstrating PTMs at lysine residues and microRNAs that are involved in reprogramming of cancer central carbon metabolism, and summarize the effect of these modifications according to different parts of central carbon metabolic pathway. Moreover, we provide an updated overview of the compounds or agents targeting central carbon metabolism in cancer. Given that the heterogeneity of cancer biology, a combination of these novel therapeutics and standard chemotherapeutic agents may obtain better benefit and overcome drug resistance. Finally, this review discusses the challenges and some new steps that may further advance this field. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.

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Keywords:  Cancer; glutaminolysis; glycolysis; lysine.; metabolism; micrornas; pentose phosphate pathway; posttranslationalzzm321990modifications; tricarboxylic acid cycle

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Year:  2017        PMID: 28356004     DOI: 10.2174/1871520617666170327110712

Source DB:  PubMed          Journal:  Anticancer Agents Med Chem        ISSN: 1871-5206            Impact factor:   2.505


  2 in total

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Authors:  Jiaxing He; Weiqin Chang; Chunyang Feng; Manhua Cui; Tianmin Xu
Journal:  Int J Genomics       Date:  2018-03-27       Impact factor: 2.326

2.  Remarkable immune and clinical value of novel ferroptosis-related genes in glioma.

Authors:  Xiaoyan Gao; Jiazheng Zhao; Litao Jia; Qiushi Zhang
Journal:  Sci Rep       Date:  2022-07-27       Impact factor: 4.996

  2 in total

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