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MYC Rules: Leading Glutamine Metabolism toward a Distinct Cancer Cell Phenotype

期刊

CANCERS
卷 13, 期 17, 页码 -

出版社

MDPI
DOI: 10.3390/cancers13174484

关键词

oncogene; MYC; glutamine metabolism

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资金

  1. Chaire de recherche en hepatologie Novartis-Fondation canadienne du foie de l'Universite de Montreal

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In the last decade, metabolic reprogramming has been recognized as a key characteristic of cancer cells, with the MYC oncogene playing a crucial role in regulating differential cancer cell metabolism, particularly through the involvement of glutamine. Understanding the metabolic pathways, such as glutaminolysis, controlled by MYC activation provides insights into the potential vulnerabilities of cancer cells from a metabolic perspective.
Simple Summary In the last decade, metabolic reprogramming has emerged as a driving characteristic of cancer cells. The MYC oncogene, a transcription factor, has become of growing interest as a fundamental driver of differential cancer cell metabolism. Furthermore, the non-essential amino acid glutamine is deemed to be an important nutrient for cancer cells. In fact, glutamine can integrate into a wide variety of metabolic pathways, from energy metabolism to nucleotide synthesis. This review offers a comprehensive and specific overview of recent discoveries in the regulation of MYC oncogene activation on glutamine metabolism in cancer cells. Metabolic reprogramming and deregulated cellular energetics are hallmarks of cancer. The aberrant metabolism of cancer cells is thought to be the product of differential oncogene activation and tumor suppressor gene inactivation. MYC is one of the most important oncogenic drivers, its activation being reported in a variety of cancer types and sub-types, among which are the most prevalent and aggressive of all malignancies. This review aims to offer a comprehensive overview and highlight the importance of the c-Myc transcription factor on the regulation of metabolic pathways, in particular that of glutamine and glutaminolysis. Glutamine can be extensively metabolized into a variety of substrates and be integrated in a complex metabolic network inside the cell, from energy metabolism to nucleotide and non-essential amino acid synthesis. Together, understanding metabolic reprogramming and its underlying genetic makeup, such as MYC activation, allows for a better understanding of the cancer cell phenotype and thus of the potential vulnerabilities of cancers from a metabolic standpoint.

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