AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells
- PMID: 30702927
- DOI: 10.1096/fj.201801559RR
AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells
Abstract
It has been shown that 5-amino-4-imidazolecarboxamide riboside (AICAr) can inhibit cell proliferation and induce apoptosis in childhood acute lymphoblastic leukemia (ALL) cells. Although AICAr could regulate cellular energy metabolism by activating AMPK, the cytotoxic mechanisms of AICAr are still unclear. Here, we knocked out TP53 or PRKAA1 gene (encoding AMPKα1) in NALM-6 and Reh cells by using the clustered regularly interspaced short palindromic repeats/Cas9 system and found that AICAr-induced proliferation inhibition was independent of AMPK activation but dependent on p53. Liquid chromatography-mass spectrometry analysis of nucleotide metabolites indicated that AICAr caused an increase in adenosine triphosphate, deoxyadenosine triphosphate, and deoxyguanosine triphosphate levels by up-regulating purine biosynthesis, while AICAr led to a decrease in cytidine triphosphate, uridine triphosphate, deoxycytidine triphosphate, and deoxythymidine triphosphate levels because of reduced phosphoribosyl pyrophosphate production, which consequently impaired the pyrimidine biosynthesis. Ribonucleoside triphosphate (NTP) pool imbalances suppressed the rRNA transcription efficiency. Furthermore, deoxy-ribonucleoside triphosphate (dNTP) pool imbalances induced DNA replication stress and DNA double-strand breaks, followed by cell cycle arrest and apoptosis in ALL cells. Exogenous uridine could rebalance the NTP and dNTP pools by supplementing pyrimidine and then attenuate AICAr-induced cytotoxicity. Our data indicate that RNA transcription inhibition and DNA replication stress induced by NTP and dNTP pool imbalances might play a key role in AICAr-mediated cytotoxic effects on ALL cells, suggesting a potential clinical application of AICAr in future ALL therapy.-Du, L., Yang, F., Fang, H., Sun, H., Chen, Y., Xu, Y., Li, H., Zheng, L., Zhou, B.-B. S. AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells.
Keywords: apoptosis; cell cycle; nucleotide imbalances.
Similar articles
-
AICAr, a Widely Used AMPK Activator with Important AMPK-Independent Effects: A Systematic Review.Cells. 2021 May 4;10(5):1095. doi: 10.3390/cells10051095. Cells. 2021. PMID: 34064363 Free PMC article.
-
Cytotoxic effect of 5-aminoimidazole-4-carboxamide-1-beta-4-ribofuranoside (AICAR) on childhood acute lymphoblastic leukemia (ALL) cells: implication for targeted therapy.Mol Cancer. 2007 Jul 10;6:46. doi: 10.1186/1476-4598-6-46. Mol Cancer. 2007. PMID: 17623090 Free PMC article.
-
AMPK and Akt determine apoptotic cell death following perturbations of one-carbon metabolism by regulating ER stress in acute lymphoblastic leukemia.Mol Cancer Ther. 2011 Mar;10(3):437-47. doi: 10.1158/1535-7163.MCT-10-0777. Epub 2011 Jan 24. Mol Cancer Ther. 2011. PMID: 21262957 Free PMC article.
-
Adenosine monophosphate-activated protein kinase suppresses vascular smooth muscle cell proliferation through the inhibition of cell cycle progression.Circ Res. 2005 Oct 14;97(8):837-44. doi: 10.1161/01.RES.0000185823.73556.06. Epub 2005 Sep 8. Circ Res. 2005. PMID: 16151020
-
Regulation by degradation, a cellular defense against deoxyribonucleotide pool imbalances.Mutat Res. 2010 Nov 28;703(1):2-10. doi: 10.1016/j.mrgentox.2010.06.002. Epub 2010 Jun 16. Mutat Res. 2010. PMID: 20561600 Review.
Cited by
-
AICAr, a Widely Used AMPK Activator with Important AMPK-Independent Effects: A Systematic Review.Cells. 2021 May 4;10(5):1095. doi: 10.3390/cells10051095. Cells. 2021. PMID: 34064363 Free PMC article.
-
The effect of AMP kinase activation on differentiation and maturation of osteoblast cultured on titanium plate.J Dent Sci. 2022 Jul;17(3):1225-1231. doi: 10.1016/j.jds.2021.12.003. Epub 2021 Dec 20. J Dent Sci. 2022. PMID: 35784162 Free PMC article.
-
Antitumor Mechanism of Hydroxycamptothecin via the Metabolic Perturbation of Ribonucleotide and Deoxyribonucleotide in Human Colorectal Carcinoma Cells.Molecules. 2021 Aug 13;26(16):4902. doi: 10.3390/molecules26164902. Molecules. 2021. PMID: 34443490 Free PMC article.
-
Fabrication of a 3D bioprinting model for posterior capsule opacification using GelMA and PLMA hydrogel-coated resin.Regen Biomater. 2024 Mar 1;11:rbae020. doi: 10.1093/rb/rbae020. eCollection 2024. Regen Biomater. 2024. PMID: 38529352 Free PMC article.
-
The ribonucleoside AICAr induces differentiation of myeloid leukemia by activating the ATR/Chk1 via pyrimidine depletion.J Biol Chem. 2019 Oct 18;294(42):15257-15270. doi: 10.1074/jbc.RA119.009396. Epub 2019 Aug 20. J Biol Chem. 2019. PMID: 31431503 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous