Probing Anti-Leukemic Metabolites from Marine-Derived Streptomyces sp. LY1209.
You-Ying ChenLo-Yun ChenPo-Jen ChenMohamed El-ShazlyBo-Rong PengYu-Cheng ChenChun-Han SuJui-Hsin SuPing-Jyun SungPei-Tzu YenLung-Shuo WangKuei-Hung LaiPublished in: Metabolites (2022)
The unmet need for specific anti-leukemic agents for the treatment of acute lymphoblastic leukemia led us to screen a variety of marine-derived bacteria. The fermentation broth extract of Streptomyces sp. LY1209 exhibited the most potent anti-proliferative effect against Molt 4 leukemia cells. A chromatographic anti-proliferative profiling approach was applied to characterize the metabolites with bioactive potential. Among all the metabolites, the major anti-leukemic constituents were staurosporine and a series of diketopiperazines (DKPs), including one novel and two known DKPs identified from nature for the first time. The structures of these compounds were identified using extensive spectroscopic analysis. The anti-proliferative potential of these metabolites against the Molt 4 cancer cell line was also determined. According to the in silico analysis utilizing a chemical global positioning system for natural products (ChemGPS-NP), it was suggested that these DKPs are potential anti-microtubule and alkylating agents, while staurosporine was proposed to be a tyrosine kinase inhibitor. Our findings not only identified a series of anti-proliferative metabolites, but also suggested a strategic workflow for the future discovery of natural product drug leads.
Keyphrases
- ms ms
- acute lymphoblastic leukemia
- acute myeloid leukemia
- oxidative stress
- squamous cell carcinoma
- molecular docking
- high throughput
- emergency department
- cell proliferation
- young adults
- papillary thyroid
- single cell
- allogeneic hematopoietic stem cell transplantation
- single molecule
- smoking cessation
- signaling pathway
- adverse drug