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Research Article Open access CC BY 4.0

A Computational Modeling Study on the Biomolecular Interactions of the Phytoconstituents of Nigella sativa with Anti-Apoptotic Proteins Mcl-1 and Bcl-x1

Olajumoke B. Oladapo, Toheeb A. Jumah, Justine U. Egbe, Jude O. Uzoechina, Aderonke E. Fakayode, Muhammad I. Adeyemi, Oluwaseyi P. Olaniyan, Chimunda A. Solomon, Zion O. Oluwasegun, Damilola M. Olatunde, Uche O. Arunsi, Samuel O. Olubode, Precious A. Akinnusi, Toheeb A Balogun, Sunday B. Akinde

Asian Journal of Biochemistry, Genetics and Molecular Biology · pp. 28–41 · Published 4 Jun 2024

10.9734/ajbgmb/2024/v16i7389

Abstract

Cancer is the second leading cause of mortality worldwide. The strictly controlled physiological process of apoptosis is required for immune system function, maintenance of tissue homeostasis, and appropriate embryonic development. Anti-apoptotic proteins such as Bcl-xL and Mcl-1 are potent new anticancer targets. The inhibitory effect of the apparently therapeutic plant Nigella sativa on these targets is investigated using a molecular modeling approach in this work. From the molecular docking, we predict that seven compounds; apigenin, chlorogenic acid, hesperidin, quercetin, quercitrin, kaempferol, and rutin may have greater inhibitory potential against the target protein. These compounds have higher docking scores thus indicating higher binding affinities when compared to co-crystallized compounds. The co-compounds were crystallized with the standards, which served as the baselines for comparison studies. This result shows that that Nigella sativa compounds may be a potential anticancer drug that targets the anti-apoptotic protein. Targeting anti-apoptotic proteins provides clinical studies with the opportunity to evaluate for possible anti-cancer potential in the plant via other experimental models like rats and cancer cell lines. Using phytomedicines can equally augment existing therapy to provide synergistic anti-cancer effect when combined with existing drugs thereby enhancing therapy efficacy and because medicinal plants has lots of phytoconstituents, its use in this research can provide benefits of targeting multiple anti-apoptotic proteins thereby enhancing therapeutic effect unlike some conventional drugs that are mostly single targeting.

Anti-apoptotic proteins Mcl-1, Bcl-xL molecular docking ADMET Nigella sativa

References (26)

  1. 1 SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules [DOI]
  2. 2 Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018 [DOI]
  3. 3 Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings [DOI]
  4. 4 ProTox-II: a webserver for the prediction of toxicity of chemicals [DOI]
  5. 5 The influence of lipophilicity in drug discovery and design [DOI]
  6. 6 Apoptosis (programmed cell death) and its signals - A review [DOI]
  7. 7 Apoptosis Deregulation and the Development of Cancer Multi-Drug Resistance [DOI]
  8. 8 Cancer as a Metabolic Disorder [DOI]
  9. 9 MCL-1 inhibitors, fast-lane development of a new class of anti-cancer agents [DOI]
  10. 10 Inhibiting the inhibitors: Targeting anti-apoptotic proteins in cancer and therapy resistance [DOI]
  11. 11 Saga of Mcl-1: regulation from transcription to degradation [DOI]
  12. 12 Modulation of the Apoptosis Gene Bcl-x Function Through Alternative Splicing [DOI]
  13. 13 Discovery of PROTAC BCL-XL degraders as potent anticancer agents with low on-target platelet toxicity [DOI]
  14. 14 Dermatological effects of Nigella sativa [DOI]
  15. 15 Bcl-2 Family of Proteins in the Control of Mitochondrial Calcium Signalling: An Old Chap with New Roles [DOI]
  16. 16 Interactions of multidomain pro-apoptotic and anti-apoptotic proteins in cancer cell death [DOI]
  17. 17 Rab GTPases: Emerging Oncogenes and Tumor Suppressive Regulators for the Editing of Survival Pathways in Cancer [DOI]
  18. 18 Swiss ADME prediction of phytochemicals present in Butea monosperma (Lam.) Taub
  19. 19 Design and synthesis of 1,4-disubstituted 1,2,3-triazoles: Biological evaluation, in silico molecular docking and ADME screening [DOI]
  20. 20 Simulation Models for Prediction of Bioavailability of Medicinal Drugs—the Interface Between Experiment and Computation [DOI]
  21. 21 Swiss ADME properties screening of the phytochemical compounds present in Bauhinia acuminata [DOI]
  22. 22 Computational Quantum Chemical Study, Drug-Likeness and In Silico Cytotoxicity Evaluation of Some Steroidal Anti-Inflammatory Drugs [DOI]
  23. 23 Physiological Functions of Mcl-1: Insights From Genetic Mouse Models [DOI]
  24. 24 Potential Inhibitory Biomolecular Interactions of Natural Compounds With Different Molecular Targets of Diabetes [DOI]
  25. 25 Synergistic activity of ABT-263 and ONC201/TIC10 against solid tumor cell lines is associated with suppression of anti-apoptotic Mcl-1, BAG3, pAkt, and upregulation of pro-apoptotic Noxa and Bax cleavage during apoptosis.
  26. 26 Biological and chemical evaluations of the seeds of Nigella sativa Linn (Ranunculaceae)

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