Anithiactin D, a Phenylthiazole Natural Product from Mudflat-Derived Streptomyces sp., Suppresses Motility of Cancer Cells.
Sultan PulatInho YangJihye LeeSunghoon HwangRui ZhouChathurika D B GamageMücahit Varlıİsa TaşYi YangSo-Yeon ParkAhreum HongJeong-Hyeon KimDong-Chan OhHangun KimSang-Jip NamHeonjoong KangPublished in: Marine drugs (2024)
Anithiactin D ( 1 ), a 2-phenylthiazole class of natural products, was isolated from marine mudflat-derived actinomycetes Streptomyces sp. 10A085. The chemical structure of 1 was elucidated based on the interpretation of NMR and MS data. The absolute configuration of 1 was determined by comparing the experimental and calculated electronic circular dichroism (ECD) spectral data. Anithiactin D ( 1 ) significantly decreased cancer cell migration and invasion activities at a concentration of 5 μM via downregulation of the epithelial-to-mesenchymal transition (EMT) markers in A549, AGS, and Caco-2 cell lines. Moreover, 1 inhibited the activity of Rho GTPases, including Rac1 and RhoA in the A549 cell line, suppressed RhoA in AGS and Caco-2 cell lines, and decreased the mRNA expression levels of some matrix metalloproteinases (MMPs) in AGS and Caco-2 cell lines. Thus 1 , which is a new entity of the 2-phenylthiazole class of natural products with a unique aniline-indole fused moiety, is a potent inhibitor of the motility of cancer cells.
Keyphrases
- electronic health record
- signaling pathway
- biofilm formation
- big data
- epithelial mesenchymal transition
- magnetic resonance
- multiple sclerosis
- mass spectrometry
- high resolution
- cell proliferation
- optical coherence tomography
- ms ms
- data analysis
- staphylococcus aureus
- pseudomonas aeruginosa
- smooth muscle
- solid state
- cystic fibrosis