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Targeting the glutamine-arginine-proline metabolism axis in cancer.
Wang, Di; Duan, Jiang-Jie; Guo, Yu-Feng; Chen, Jun-Jie; Chen, Tian-Qing; Wang, Jun; Yu, Shi-Cang.
Afiliação
  • Wang D; Department of Stem Cell and Regenerative Medicine, Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
  • Duan JJ; International Joint Research Center for Precision Biotherapy, Ministry of Science and Technology, Chongqing, China.
  • Guo YF; Key Laboratory of Cancer Immunopathology, Ministry of Education, Chongqing, China.
  • Chen JJ; Department of Stem Cell and Regenerative Medicine, Institute of Pathology and Southwest Cancer Center, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
  • Chen TQ; International Joint Research Center for Precision Biotherapy, Ministry of Science and Technology, Chongqing, China.
  • Wang J; Key Laboratory of Cancer Immunopathology, Ministry of Education, Chongqing, China.
  • Yu SC; Jin-feng Laboratory, Chongqing, China.
J Enzyme Inhib Med Chem ; 39(1): 2367129, 2024 Dec.
Article em En | MEDLINE | ID: mdl-39051546
ABSTRACT
Metabolic abnormalities are an important feature of tumours. The glutamine-arginine-proline axis is an important node of cancer metabolism and plays a major role in amino acid metabolism. This axis also acts as a scaffold for the synthesis of other nonessential amino acids and essential metabolites. In this paper, we briefly review (1) the glutamine addiction exhibited by tumour cells with accelerated glutamine transport and metabolism; (2) the methods regulating extracellular glutamine entry, intracellular glutamine synthesis and the fate of intracellular glutamine; (3) the glutamine, proline and arginine metabolic pathways and their interaction; and (4) the research progress in tumour therapy targeting the glutamine-arginine-proline metabolic system, with a focus on summarising the therapeutic research progress of strategies targeting of one of the key enzymes of this metabolic system, P5CS (ALDH18A1). This review provides a new basis for treatments targeting the metabolic characteristics of tumours.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arginina / Prolina / Glutamina / Neoplasias Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arginina / Prolina / Glutamina / Neoplasias Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article