Untargeted Metabolomics Identifies Key Metabolic Pathways Altered by Thymoquinone in Leukemic Cancer Cells

被引:18
作者
AlGhamdi, Asma Ahmed [1 ]
Mohammed, Mohammed Razeeth Shait [1 ,2 ]
Zamzami, Mazin A. [1 ,2 ,3 ]
Al-Malki, Abdulrahman L. [1 ]
Qari, Mohamad Hasan [4 ]
Khan, Mohammad Imran [1 ,2 ,3 ]
Choudhry, Hani [1 ,2 ,3 ]
机构
[1] King Abdulaziz Univ, Dept Biochem, Fac Sci, Jeddah 21589, Saudi Arabia
[2] King Abdulaziz Univ, Dept Biochem, Canc Metab & Epigenet Unit, Fac Sci, Jeddah 21589, Saudi Arabia
[3] King Abdulaziz Univ, Canc & Mutagenesis Res Unit, King Fahd Med Res Ctr, Jeddah 21589, Saudi Arabia
[4] King Abdulaziz Univ, King Abdulaziz Univ Hosp, Dept Hematol, Fac Med, Jeddah 21589, Saudi Arabia
关键词
thymoquinone; leukemia; metabolites; LC-MS/MS; metabolism; DNA damage; THYMINE GLYCOL; DEPLETION;
D O I
10.3390/nu12061792
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Thymoquinone (TQ), a naturally occurring anticancer compound extracted fromNigella sativaoil, 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.
引用
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页码:1 / 16
页数:16
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