From the Inside Out: Exposing the Roles of Urea Cycle Enzymes in Tumors and Their Micro and Macro Environments

被引:3
作者
Hajaj, Emma [1 ]
Pozzi, Sabina [1 ]
Erez, Ayelet [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-7610001 Rehovot, Israel
基金
以色列科学基金会;
关键词
ARGININOSUCCINATE LYASE; ARGINASE-I; ARGININE DEPRIVATION; SUPPRESSOR-CELLS; NITRIC-OXIDE; GLUTAMINE-SYNTHETASE; ADENOSINE RECEPTORS; CANCER; METABOLISM; EXPRESSION;
D O I
10.1101/cshperspect.a041538
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Catabolic pathways change in anabolic diseases such as cancer to maintain metabolic homeostasis. The liver urea cycle (UC) is the main catabolic pathway for disposing excess nitrogen. Outside the liver, the UC enzymes are differentially expressed based on each tissue's needs for UC intermediates. In tumors, there are changes in the expression of UC enzymes selected for promoting tumorigenesis by increasing the availability of essential UC substrates and products. Consequently, there are compensatory changes in the expression of UC enzymes in the cells that compose the tumor microenvironment. Moreover, extrahepatic tumors induce changes in the expression of the liver UC, which contribute to the systemic manifestations of cancer, such as weight loss. Here, we review the multilayer changes in the expression of UC enzymes throughout carcinogenesis. Understanding the changes in UC expression in the tumor and its micro and macro environment can help identify biomarkers for early cancer diagnosis and vulnerabilities that can be targeted for therapy.
引用
收藏
页数:17
相关论文
共 131 条
[1]   Arginine-Dual Roles as an Onconutrient and Immunonutrient [J].
Albaugh, Vance L. ;
Pinzon-Guzman, Carolina ;
Barbul, Adrian .
JOURNAL OF SURGICAL ONCOLOGY, 2017, 115 (03) :273-280
[2]   Prognostic and Therapeutic Impact of Argininosuccinate Synthetase 1 Control in Bladder Cancer as Monitored Longitudinally by PET Imaging [J].
Allen, Michael D. ;
Phuong Luong ;
Hudson, Chantelle ;
Leyton, Julius ;
Delage, Barbara ;
Ghazaly, Essam ;
Cutts, Rosalind ;
Yuan, Ming ;
Syed, Nelofer ;
Lo Nigro, Cristiana ;
Lattanzio, Laura ;
Chmielewska-Kassassir, Malgorzata ;
Tomlinson, Ian ;
Roylance, Rebecca ;
Whitaker, Hayley C. ;
Warren, Anne Y. ;
Neal, David ;
Frezza, Christian ;
Beltran, Luis ;
Jones, Louise J. ;
Chelala, Claude ;
Wu, Bor-Wen ;
Bomalaski, John S. ;
Jackson, Robert C. ;
Lu, Yong-Jie ;
Crook, Tim ;
Lemoine, Nicholas R. ;
Mather, Stephen ;
Foster, Julie ;
Sosabowski, Jane ;
Avril, Norbert ;
Li, Chien-Feng ;
Szlosarek, Peter W. .
CANCER RESEARCH, 2014, 74 (03) :896-907
[3]   Next steps for clinical translation of adenosine pathway inhibition in cancer immunotherapy [J].
Augustin, Ryan C. ;
Leone, Robert D. ;
Naing, Aung ;
Fong, Lawrence ;
Bao, Riyue ;
Luke, Jason J. .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2022, 10 (02)
[4]   Urea as a By-Product of Ammonia Metabolism Can Be a Potential Serum Biomarker of Hepatocellular Carcinoma [J].
Bai, Changsen ;
Wang, Hailong ;
Dong, Dong ;
Li, Tong ;
Yu, Zhi ;
Guo, Junfei ;
Zhou, Wei ;
Li, Ding ;
Yan, Ruochen ;
Wang, Liyan ;
Wang, Zhaosong ;
Li, Yueguo ;
Ren, Li .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
[5]   Argininosuccinate Synthase 1 is a Metabolic Regulator of Colorectal Cancer Pathogenicity [J].
Bateman, Leslie A. ;
Ku, Wan-Min ;
Heslin, Martin J. ;
Contreras, Carlo M. ;
Skibola, Christine F. ;
Nomura, Daniel K. .
ACS CHEMICAL BIOLOGY, 2017, 12 (04) :905-911
[6]   Tumor-Stroma Mechanics Coordinate Amino Acid Availability to Sustain Tumor Growth and Malignancy [J].
Bertero, Thomas ;
Oldham, William M. ;
Grasset, Eloise M. ;
Bourget, Isabelle ;
Boulter, Etienne ;
Pisano, Sabrina ;
Hofman, Paul ;
Bellvert, Floriant ;
Meneguzzi, Guerrino ;
Bulavin, Dmitry, V ;
Estrach, Soline ;
Feral, Chloe C. ;
Chan, Stephen Y. ;
Bozec, Alexandre ;
Gaggioli, Cedric .
CELL METABOLISM, 2019, 29 (01) :124-+
[7]   INTESTINAL ARGININE METABOLISM DURING DEVELOPMENT - EVIDENCE FOR DE-NOVO SYNTHESIS OF L-ARGININE IN NEWBORN PIG ENTEROCYTES [J].
BLACHIER, F ;
MRABETTOUIL, H ;
POSHO, L ;
DARCYVRILLON, B ;
DUEE, PH .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 216 (01) :109-117
[8]   PHARMACOLOGY OF ADENOSINE RECEPTORS: THE STATE OF THE ART [J].
Borea, Pier Andrea ;
Gessi, Stefania ;
Merighi, Stefania ;
Vincenzi, Fabrizio ;
Varani, Katia .
PHYSIOLOGICAL REVIEWS, 2018, 98 (03) :1591-1625
[9]   Boosting antitumor responses of T lymphocytes infiltrating human prostate cancers [J].
Bronte, V ;
Kasic, T ;
Gri, G ;
Gallana, K ;
Borsellino, G ;
Marigo, I ;
Battistini, L ;
Iafrate, M ;
Prayer-Galetti, T ;
Pagano, F ;
Viola, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 2005, 201 (08) :1257-1268
[10]   β-Adrenergic Signaling in Mice Housed at Standard Temperatures Suppresses an Effector Phenotype in CD8+ T Cells and Undermines Checkpoint Inhibitor Therapy [J].
Bucsek, Mark J. ;
Qiao, Guanxi ;
MacDonald, Cameron R. ;
Giridharan, Thejaswini ;
Evans, Lauren ;
Niedzwecki, Brian ;
Liu, Haichao ;
Kokolus, Kathleen M. ;
Eng, Jason W. -L. ;
Messmer, Michelle N. ;
Attwood, Kristopher ;
Abrams, Scott I. ;
Hylander, Bonnie L. ;
Repasky, Elizabeth A. .
CANCER RESEARCH, 2017, 77 (20) :5639-5651