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Assessment of the Metabolic Profile of Primary Leukemia Cells
Published on: November 21, 2018
Untargeted Metabolomics Identifies Key Metabolic Pathways Altered by Thymoquinone in Leukemic Cancer Cells
Asma Ahmed AlGhamdi1, Mohammed Razeeth Shait Mohammed1,2, Mazin A Zamzami1,2,3
1Biochemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia.
Abstract:
Thymoquinone (TQ), a naturally occurring anticancer compound extracted from Nigella sativa oil, has been extensively reported to possess potent anti-cancer properties. Experimental studies showed the anti-proliferative, pro-apoptotic, and anti-metastatic effects of TQ on different cancer cells. One of the possible mechanisms underlying these effects includes alteration in key metabolic pathways that are critical for cancer cell survival. However, an extensive landscape of the metabolites altered by TQ in cancer cells remains elusive. Here, we performed an untargeted metabolomics study using leukemic cancer cell lines during treatment with TQ and found alteration in approximately 335 metabolites. Pathway analysis showed alteration in key metabolic pathways like TCA cycle, amino acid metabolism, sphingolipid metabolism and nucleotide metabolism, which are critical for leukemic cell survival and death. We found a dramatic increase in metabolites like thymine glycol in TQ-treated cancer cells, a metabolite known to induce DNA damage and apoptosis. Similarly, we observed a sharp decline in cellular guanine levels, important for leukemic cancer cell survival. Overall, we provided an extensive metabolic landscape of leukemic cancer cells and identified the key metabolites and pathways altered, which could be critical and responsible for the anti-proliferative function of TQ.
Insights
Thymoquinone (TQ) alters 335 metabolites in leukemia cells, impacting critical pathways like nucleotide metabolism. This reveals TQ
Area of Science:
- Biochemistry
- Cancer Biology
- Metabolomics
Background:
- Thymoquinone (TQ), derived from Nigella sativa, exhibits anticancer properties.
- TQ's anti-proliferative, pro-apoptotic, and anti-metastatic effects are documented.
- Mechanisms may involve metabolic pathway alterations, but a comprehensive view is lacking.
Purpose of the Study:
- To elucidate the metabolic landscape altered by TQ in leukemic cells.
- To identify key metabolites and pathways affected by TQ treatment.
- To understand TQ's anti-proliferative mechanisms via metabolomics.
Main Methods:
- Untargeted metabolomics approach.
- Utilized leukemic cancer cell lines.
- Analyzed metabolic alterations following TQ treatment.
Main Results:
- Identified alterations in approximately 335 metabolites.
- Pathway analysis revealed significant changes in TCA cycle, amino acid, sphingolipid, and nucleotide metabolism.
- Observed increased thymine glycol (DNA damage inducer) and decreased guanine levels.
Conclusions:
- TQ significantly alters the metabolome of leukemic cells.
- Metabolic pathway dysregulation, particularly in nucleotide metabolism, is implicated in TQ's anti-cancer effects.
- TQ's ability to induce DNA damage and apoptosis is linked to specific metabolite changes.
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