IDEAS home Printed from https://ideas.repec.org/a/bjc/journl/v11y2024i11p38-45.html
   My bibliography  Save this article

Targeting the AKT Pathway as a Therapeutic Strategy for Hepatocellular Carcinoma

Author

Listed:
  • Oluseyi Adeboye Akinloye

    (Department of Biochemistry, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria)

  • Adewumi Kamarudeen Aremu

    (1Department of Biochemistry, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria Department of Basic Science, Kwara State College of Education, Oro, Kwara State, Nigeria)

  • Ibukun Dorcas Akinloye

    (Department of Biochemistry, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria)

  • Jacob Kehinde Akintunde

    (Department of Biochemistry, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria)

  • Antiya Moses Ceaser

    (Department of Biochemistry, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria)

  • Olajire Moshood Olaniyi

    (Department of Veterinary Pathology, Federal University of Agriculture, Abeokuta, Ogun State, Nigeria)

Abstract

Hepatocellular carcinoma (HCC), one of the most common cancers of the liver has been on the rise globally and is complicated by drug resistance in treatment targets and pathway interactions such as the Akt pathway. Akt-1 protein also known as serine/threonine kinase is a good target for designing drugs for hepatocellular carcinoma. It controls cell development, survival, proliferation, glycogen consumption, and apoptosis. The overexpression of Akt-1 is a hallmark of various cancers including HCC, and plays a crucial role in tumorigenesis and cancer progression. The 3D crystal structure of human Akt-1 with an allosteric inhibitor was downloaded from a protein data bank. The preparation of ligands was done by downloading structures from the PubChem database and converted to 3D using Open Babel. In this study, phytochemicals (ligands) from some Nigerian medicinal plants were docked against the binding pocket of Akt 1 using virtual high throughput screening. Validation of docking results was done to determine the accuracy of the docking methods. The drug-like properties of the lead compounds and the standard drug were tested by employing the Lipinski rule of five. Silymarin has the highest docking score of -10.6 kcal/mol and was found to be the lead compound as a potential inhibitor with the best absorption, distribution, metabolism, and excretion properties. Silymarin interactions with key amino acid residues in the active sites were determined and compared with the reference drug, sorafenib. It was found that both silymarin and sorafenib exhibit similar interactions with the formation of hydrogen bonds, pi-cation, and pi-pi interactions. Silymarin has a relatively better inhibitory and pharmacokinetic profile than, vicenin, epig allocate chin-3-gallate, ginsenoside, and palstatin, thus it can be a useful therapeutic candidate in the treatment of HCC.

Suggested Citation

  • Oluseyi Adeboye Akinloye & Adewumi Kamarudeen Aremu & Ibukun Dorcas Akinloye & Jacob Kehinde Akintunde & Antiya Moses Ceaser & Olajire Moshood Olaniyi, 2024. "Targeting the AKT Pathway as a Therapeutic Strategy for Hepatocellular Carcinoma," International Journal of Research and Scientific Innovation, International Journal of Research and Scientific Innovation (IJRSI), vol. 11(11), pages 38-45, November.
  • Handle: RePEc:bjc:journl:v:11:y:2024:i:11:p:38-45
    as

    Download full text from publisher

    File URL: https://www.rsisinternational.org/journals/ijrsi/digital-library/volume-11-issue-11/38-45.pdf
    Download Restriction: no

    File URL: https://rsisinternational.org/journals/ijrsi/articles/targeting-the-akt-pathway-as-a-therapeutic-strategy-for-hepatocellular-carcinoma/
    Download Restriction: no
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:bjc:journl:v:11:y:2024:i:11:p:38-45. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Dr. Renu Malsaria (email available below). General contact details of provider: https://rsisinternational.org/journals/ijrsi/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.