Nummularic acid, a triterpenoid, from the medicinal plant Fraxinus xanthoxyloides, induces energy crisis to suppress growth of prostate cancer cells

• Published in: Molecular carcinogenesis 2018-10, Vol.57 (10), p.1267-1277
• Main Authors: Younis, Tahira, Khan, Mohammad I., Khan, Muhammad R., Rasul, Azhar, Majid, Muhammad, Adhami, Vaqar M., Mukhtar, Hasan
• Format: Article
• Language: English
• Subjects: 5′AMP activated kinase; Acetyl-CoA Carboxylase - metabolism; Acids; Activation; Adenosine diphosphate; Adenosine kinase; AMP; AMPK; Antifungal agents; Apoptosis; Apoptosis - drug effects; Cell death; Cell Line, Tumor; Cell proliferation; Cell Proliferation - drug effects; Energy; Energy metabolism; Energy Metabolism - drug effects; Fraxinus; Fraxinus - chemistry; Glutamine; Glycolysis; Herbal medicine; Humans; Invasiveness; Kinases; Male; Medicinal plants; Metabolism; Metabolomics; Metabolomics - methods; Molecular Structure; Oxygen consumption; Peptides, Cyclic; Phosphorylation; Phosphorylation - drug effects; Plants, Medicinal - chemistry; proliferation; Prostate; Prostate cancer; Prostatic Neoplasms - metabolism; Prostatic Neoplasms - pathology; Protein kinase; Triterpenes - chemistry; Triterpenes - pharmacology
• ISSN: 0899-1987; 1098-2744
• DOI: 10.1002/mc.22841

We recently identified and characterized nummularic acid (NA) as a major chemical constituent of Fraxinus xanthoxyloides, a medicinal plant used for over hundred years in traditional medicine. In this study, we describe its potential anti‐cancer activity using prostate cancer (PCa) cells as a model. We found that NA treatment (5‐60 μM) significantly reduced the proliferation and colony formation capabilities of PCa DU145 and C4‐2 cells in a time and dose dependent manner, reduced the migratory and invasive properties and increased apoptotic cell population. Mechanistically, we found that NA treatment to PCa cells resulted in a sustained activation of adenosine monophosphate‐activated protein kinase (AMPK). NA simultaneously increased acetyl CoA carboxylase phosphorylation and decreased pS6 phosphorylation, the two major substrates of AMPK. Further, NA treatment significantly elevated the cellular ADP/ATP ratio and altered glycolytic rate. We further observed a reversible decrease in oxygen consumption rate in NA treated cells when compared to the control. Finally, we performed global untargeted metabolomics which showed that NA treatment alters PCa cell metabolism at multiple sites including glycolysis, tricarboxylic acid, and glutamine metabolism which supported our observation of a possible AMPK activation. In summary, we report NA as a novel small molecule activator of AMPK that alters cellular metabolism to induce energy crisis and ultimately cancer cell death. Because of its unique mechanism NA could be potentially applicable against other cancer types.