Computational evaluation of natural compounds as potential inhibitors of human PEPCK-M: an alternative for lung cancer therapy

• Published in: Advances and applications in bioinformatics and chemistry 2019-08, Vol.12, p.15-32
• Main Authors: Baptista, Luiz Phillippe R, Sinatti, Vanessa Vc, Da Silva, Joao Hm, Dardenne, Laurent Emmanuel, Guimarães, Ana Carolina
• Format: Article
• Language: English
• Subjects: Acids; Analysis; Antimitotic agents; Antineoplastic agents; Apoptosis; Binding sites; Bioinformatics; Cancer; Cancer screening; Cancer therapies; Cancer treatment; Care and treatment; Computer applications; Criminal investigation; Death; Dextrose; Diagnosis; Drugs; Enzymes; Gluconeogenesis; Glucose; Guanosine triphosphate; Health aspects; Kinases; Lead compounds; Ligands; Lung cancer; Lung cancer, Non-small cell; Metabolism; Metabolites; Mitochondria; molecular docking; Natural products; Non-small cell lung cancer; Non-small cell lung carcinoma; Novels; Original Research; PEPCK-M; pharmacophore modeling; Phosphatase; Phosphates; Proteins; Small cell lung cancer; Tumors; virtual screening
• ISSN: 1178-6949; 1178-6949
• DOI: 10.2147/AABC.S197119

Lung cancer is the leading cause of cancer-related death worldwide. Among its subtypes, non-small cell lung cancer (NSCLC) is the most common. Recently, the mitochondrial isoform of the enzyme phosphoenolpyruvate carboxykinase (HsPEPCK-M) was identified as responsible for the metabolic adaptation in the NSCLC allowing tumor growth even under conditions of glucose deficiency. This adaptation is possible due to the role of HsPEPCK-M in gluconeogenesis, converting the oxaloacetate to phosphoenolpyruvate in the presence of GTP, which plays an important role in the energetic support of these tumors. In this context, it was shown that the inhibition or knockdown of this enzyme was able to induce apoptosis in NSCLC under low glucose conditions. In this study, novel putative inhibitors were proposed for the human PEPCK-M (HsPEPCK-M) based on a computer-aided approach. Comparative modeling was used to generate 3D models for HsPEPCK-M. Subsequently, the set of natural compounds of the ZINC database was screened against HsPEPCK-M models using structure-based pharmacophore modeling and molecular docking approaches. The selected compounds were evaluated according to its chemical diversity and clustered based on chemical similarity. The pharmacophore hypotheses, generated based on known PEPCK inhibitors, were able to select 7,124 candidate compounds. These compounds were submitted to molecular docking studies using three conformations of HsPEPCK-M generated by comparative modeling. The aim was to select compounds with high predicted binding affinity for at least one of the conformations of HsPEPCK-M. After molecular docking, 612 molecules were selected as potential inhibitors of HsPEPCK-M. These compounds were clustered according to their structural similarity. Chemical profiling and binding mode analyses of these compounds allowed the proposal of four promising compounds: ZINC01656421, ZINC895296, ZINC00895535 and ZINC02571340. These compounds may be considered as potential candidates for HsPEPCK-M inhibitors and may also be used as lead compounds for the development of novel HsPEPCK-M inhibitors.