Literature DB >> 31511353

Metabolic Flexibility in Cancer: Targeting the Pyruvate Dehydrogenase Kinase:Pyruvate Dehydrogenase Axis.

Benjamin L Woolbright1, Ganeshkumar Rajendran1, Robert A Harris2, John A Taylor3.   

Abstract

Cancer cells use alterations of normal metabolic processes to sustain proliferation indefinitely. Transcriptional and posttranscriptional control of the pyruvate dehydrogenase kinase (PDK) family is one way in which cancer cells alter normal pyruvate metabolism to fuel proliferation. PDKs can phosphorylate and inactivate the pyruvate dehydrogenase complex (PDHC), which blocks oxidative metabolism of pyruvate by the mitochondria. This process is thought to enhance cancer cell growth by promoting anabolic pathways. Inhibition of PDKs induces cell death through increased PDH activity and subsequent increases in ROS production. The use of PDK inhibitors has seen widespread success as a potential therapeutic in laboratory models of multiple cancers; however, gaps still exist in our understanding of the biology of PDK regulation and function, especially in the context of individual PDKs. Efforts are currently underway to generate PDK-specific inhibitors and delineate the roles of individual PDK isozymes in specific cancers. The goal of this review is to understand the regulation of the PDK isozyme family, their role in cancer proliferation, and how to target this pathway therapeutically to specifically and effectively reduce cancer growth. ©2019 American Association for Cancer Research.

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Year:  2019        PMID: 31511353     DOI: 10.1158/1535-7163.MCT-19-0079

Source DB:  PubMed          Journal:  Mol Cancer Ther        ISSN: 1535-7163            Impact factor:   6.261


  34 in total

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2.  Mice deficient in pyruvate dehydrogenase kinase 4 are protected against acetaminophen-induced hepatotoxicity.

Authors:  Luqi Duan; Anup Ramachandran; Jephte Y Akakpo; Benjamin L Woolbright; Yuxia Zhang; Hartmut Jaeschke
Journal:  Toxicol Appl Pharmacol       Date:  2019-12-03       Impact factor: 4.219

Review 3.  PGC-1α participates in tumor chemoresistance by regulating glucose metabolism and mitochondrial function.

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Review 4.  Dihydrolipoamide dehydrogenase, pyruvate oxidation, and acetylation-dependent mechanisms intersecting drug iatrogenesis.

Authors:  I F Duarte; J Caio; M F Moedas; L A Rodrigues; A P Leandro; I A Rivera; M F B Silva
Journal:  Cell Mol Life Sci       Date:  2021-10-31       Impact factor: 9.261

5.  Alpha-Lipoic Acid Protects Against Doxorubicin-Induced Cardiotoxicity by Regulating Pyruvate Dehydrogenase Kinase 4.

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6.  Tumor cells dictate anti-tumor immune responses by altering pyruvate utilization and succinate signaling in CD8+ T cells.

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7.  PDK4 Constitutes a Novel Prognostic Biomarker and Therapeutic Target in Gastric Cancer.

Authors:  Zimu Zhang; Shiyuan Han; Siwen Ouyang; Ziyang Zeng; Zhen Liu; Juan Sun; Weiming Kang
Journal:  Diagnostics (Basel)       Date:  2022-04-27

8.  Identification of PDHX as a metabolic target for esophageal squamous cell carcinoma.

Authors:  Jun Inoue; Masahiro Kishikawa; Hitoshi Tsuda; Yasuaki Nakajima; Takahiro Asakage; Johji Inazawa
Journal:  Cancer Sci       Date:  2021-05-24       Impact factor: 6.716

Review 9.  Reprogramming of glucose metabolism of cumulus cells and oocytes and its therapeutic significance.

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Journal:  Reprod Sci       Date:  2021-03-05       Impact factor: 3.060

Review 10.  The Metabolic Fates of Pyruvate in Normal and Neoplastic Cells.

Authors:  Edward V Prochownik; Huabo Wang
Journal:  Cells       Date:  2021-03-30       Impact factor: 6.600

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