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Design of amino acid- and carbohydrate-based anticancer drugs to inhibit polymerase η

Kalhor, S ; Sharif University of Technology | 2022

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  1. Type of Document: Article
  2. DOI: 10.1038/s41598-022-22810-z
  3. Publisher: Nature Research , 2022
  4. Abstract:
  5. DNA polymerase η (polη) is of significant value for designing new families of anticancer drugs. This protein takes a role in many stages of the cell cycle, including DNA replication, translesion DNA synthesis, and the repairing process of DNA. According to many studies, a high level of expression of polη in most cases has been associated with low rates of patients' survival, regardless of considering the stage of tumor cells. Thus, the design of new drugs with fewer side effects to inhibit polη in cancerous cells has attracted attention in recent years. This project aims to design and explore the alternative inhibitors for polη, which are based on carbohydrates and amino acids. In terms of physicochemical properties, they are similar to the traditional anticancer drugs such as Cytarabine (cytosine arabinose). These alternative inhibitors are supposed to disrupt the DNA replication process in cancerous cells and prevent the tumor cells from mitosis. These newly designed structures, which are based on natural products, are expected to be non-toxic and to have the same chemotherapeutic impact as the traditional agents. The combinatorial use of quantum mechanics studies and molecular dynamic simulation has enabled us to precisely predict the inhibition mechanism of the newly designed structure, which is based on carbohydrates and amino acids, and compare it with that of the traditional chemotherapeutic drugs such as Cytarabine. Our results suggest that the inhibitors containing the natural building blocks of amino acid and carbohydrate could be considered alternative drugs for Cytarabine to block polη. © 2022, The Author(s)
  6. Keywords:
  7. Amino acid ; Antineoplastic agent ; Carbohydrate ; Cytarabine ; Chemistry ; DNA damage ; DNA replication ; Genetics ; Human ; Metabolism ; Amino acids ; Antineoplastic agents ; Carbohydrates ; DNA ; Humans
  8. Source: Scientific Reports ; Volume 12, Issue 1 , 2022 ; 20452322 (ISSN)
  9. URL: https://pubmed.ncbi.nlm.nih.gov/36323739