AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells. Issue 3 (31st January 2019)
- Record Type:
- Journal Article
- Title:
- AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells. Issue 3 (31st January 2019)
- Main Title:
- AICAr suppresses cell proliferation by inducing NTP and dNTP pool imbalances in acute lymphoblastic leukemia cells
- Authors:
- Du, Lijuan
Yang, Fan
Fang, Houshun
Sun, Huiying
Chen, Yao
Xu, Yan
Li, Hui
Zheng, Liang
Zhou, Bin-Bing S. - Abstract:
- 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 attenuateABSTRACT: 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. FASEB J. 33, 4525–4537 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 3(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 3(2019)
- Issue Display:
- Volume 33, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 3
- Issue Sort Value:
- 2019-0033-0003-0000
- Page Start:
- 4525
- Page End:
- 4537
- Publication Date:
- 2019-01-31
- Subjects:
- cell cycle -- apoptosis -- nucleotide -- imbalances
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201801559RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13316.xml