Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Impact of Snps, Off-Targets, and Passive Permeability on Efficacy of Bcl6 Degrading Drugs Assigned by Virtual Screening and 3D-Qsar Approach Publisher Pubmed



Karimi S1 ; Shahabi F2 ; Mubarak SMH3 ; Arjmandi H4 ; Hashemi ZS5 ; Pourzardosht N6 ; Zakeri A7 ; Mahboobi M8 ; Jahangiri A8 ; Rahbar MR9 ; Khalili S7
Authors
Show Affiliations
Authors Affiliations
  1. 1. Laboratory of Mitochondrial Biology and Metabolism, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Warsaw, 02-093, Poland
  2. 2. Faculty of Advanced Technologies in Medical Sciences, Golestan University of Medical Sciences, Gorgan, Iran
  3. 3. Department of Clinical Laboratory Science, Faculty of Pharmacy, University of Kufa, Najaf, Iraq
  4. 4. Faculty of Pharmacy, Islamic Azad University of Amol Branch, Amol, Iran
  5. 5. ATMP Department, Breast Cancer Research Center, Motamed Cancer Institute, ACECR, Tehran, Iran
  6. 6. Biochemistry Department, Guilan University of Medical Sciences, Rasht, Iran
  7. 7. Department of Biology Sciences, Shahid Rajaee Teacher Training University, Tehran, Iran
  8. 8. Applied Microbiology Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, Iran
  9. 9. Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

Source: Scientific Reports Published:2022


Abstract

B-cell lymphoma 6 (BCL6) regulates various genes and is reported to be overexpressed in lymphomas and other malignancies. Thus, BCL6 inhibition or its tagging for degradation would be an amenable therapeutic approach. A library of 2500 approved drugs was employed to find BCL6 inhibitory molecules via virtual screening. Moreover, the 3D core structure of 170 BCL6 inhibitors was used to build a 3D QSAR model and predict the biological activity. The SNP database was analyzed to study the impact on the destabilization of BCL6/drug interactions. Structural similarity search and molecular docking analyses were used to assess the interaction between possible off-targets and BCL6 inhibitors. The tendency of drugs for passive membrane permeability was also analyzed. Lifitegrast (DB11611) had favorable binding properties and biological activity compared to the BI-3802. Missense SNPs were located at the essential interaction sites of the BCL6. Structural similarity search resulted in five BTB-domain containing off-target proteins. BI-3802 and Lifitegrast had similar chemical behavior and binding properties against off-target candidates. More interestingly, the binding affinity of BI-3802 (against off-targets) was higher than Lifitegrast. Energetically, Lifitegrast was less favorable for passive membrane permeability. The interaction between BCL6 and BI-3802 is more prone to SNP-derived variations. On the other hand, higher nonspecific binding of BI-3802 to off-target proteins could bring about higher undesirable properties. It should also be noted that energetically less desirable passive membrane translocation of Lifitegrast would demand drug delivery vehicles. However, further empirical evaluation of Lifitegrast would unveil its true potential. © 2022, The Author(s).
Experts (# of related papers)