Literature DB >> 32032699

Structure-based drug repositioning: Potential and limits.

Melissa F Adasme1, Daniele Parisi2, Anastasia Sveshnikova1, Michael Schroeder3.   

Abstract

Drug repositioning, the assignment of new therapeutic purposes to known drugs, is an established strategy with many repurposed drugs on the market and many more at experimental stage. We review three use cases, a herpes drug with benefits in cancer, a cancer drug with potential in autoimmune disease, and a selective and an unspecific drug binding the same target (GPCR). We explore these use cases from a structural point of view focusing on a deep understanding of the underlying drug-target interactions. We review tools and data needed for such a drug-centric structural repositioning approach. Finally, we show that the availability of data on targets is an important limiting factor to realize the full potential of structural drug-repositioning.
Copyright © 2020 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Drug repositioning; Repurposed drugs; Structure-based screening

Mesh:

Substances:

Year:  2020        PMID: 32032699     DOI: 10.1016/j.semcancer.2020.01.010

Source DB:  PubMed          Journal:  Semin Cancer Biol        ISSN: 1044-579X            Impact factor:   15.707


  5 in total

1.  Metabolic modeling-based drug repurposing in Glioblastoma.

Authors:  Claudio Tomi-Andrino; Alina Pandele; Klaus Winzer; John King; Ruman Rahman; Dong-Hyun Kim
Journal:  Sci Rep       Date:  2022-07-01       Impact factor: 4.996

2.  Repositioned Drugs for Chagas Disease Unveiled via Structure-Based Drug Repositioning.

Authors:  Melissa F Adasme; Sarah Naomi Bolz; Lauren Adelmann; Sebastian Salentin; V Joachim Haupt; Adriana Moreno-Rodríguez; Benjamín Nogueda-Torres; Verónica Castillo-Campos; Lilián Yepez-Mulia; José A De Fuentes-Vicente; Gildardo Rivera; Michael Schroeder
Journal:  Int J Mol Sci       Date:  2020-11-20       Impact factor: 5.923

3.  Low-Dose Albendazole Inhibits Epithelial-Mesenchymal Transition of Melanoma Cells by Enhancing Phosphorylated GSK-3β/Tyr216 Accumulation.

Authors:  Zhiqiang He; Shun Lei; Fucheng Liang; Liuchang Tan; Weinan Zhang; Luoyingzi Xie; Hong Zheng; Yuangang Lu
Journal:  J Oncol       Date:  2021-12-20       Impact factor: 4.375

4.  Decomposing compounds enables reconstruction of interaction fingerprints for structure-based drug screening.

Authors:  Melissa F Adasme; Sarah Naomi Bolz; Ali Al-Fatlawi; Michael Schroeder
Journal:  J Cheminform       Date:  2022-03-15       Impact factor: 5.514

5.  Virtual Screening of FDA-Approved Drugs against Triose Phosphate Isomerase from Entamoeba histolytica and Giardia lamblia Identifies Inhibitors of Their Trophozoite Growth Phase.

Authors:  Alfredo Juárez-Saldivar; Elizabeth Barbosa-Cabrera; Edgar E Lara-Ramírez; Alma D Paz-González; Ana V Martínez-Vázquez; Virgilio Bocanegra-García; Isidro Palos; Nuria E Campillo; Gildardo Rivera
Journal:  Int J Mol Sci       Date:  2021-05-31       Impact factor: 5.923

  5 in total

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