Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Structure-Activity Relationships and Drug Design01:28

Structure-Activity Relationships and Drug Design

Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Hazard Ratio01:12

Hazard Ratio

The hazard ratio (HR) is a widely used measure in clinical trials to compare the risk of events, such as death or disease recurrence, between two groups over time. It reflects the ratio of hazard rates—the instantaneous risk of the event occurring—between a treatment group and a control group. This measure provides valuable insights into the relative effectiveness of a treatment by assessing how the risk of an event differs between the two groups.
For example, in a clinical trial evaluating a...
Drug Discovery: Overview01:26

Drug Discovery: Overview

Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches01:23

Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches

Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The reticulospinal tracts are significant for the control of the anus and bladder: Insights from a complicated spinal cord stimulation case.

The journal of spinal cord medicine·2026
Same author

New insights into the interaction of the symbiotic bacterium Candidatus Erwinia dacicola with the adult olive fly Bactrocera oleae combining microscopy and proteomics analyses.

Insect biochemistry and molecular biology·2026
Same author

Building an Adverse Outcome Pathway network for COVID-19.

Frontiers in systems biology·2025
Same author

Broadening the Nicotiana benthamiana research toolbox through the generation of dicer-like mutants using CRISPR/Cas9 approaches.

Plant science : an international journal of experimental plant biology·2025
Same author

dsRNAEngineer: a web-based tool of comprehensive dsRNA design for pest control.

Trends in biotechnology·2025
Same author

Spinal Cord Stimulation Restores Pyramidal Activity in a Patient With Paraplegia With Spinal Cord Injury.

Neuromodulation : journal of the International Neuromodulation Society·2024

Related Experiment Video

Updated: Jun 3, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Drug repurposing and adverse event prediction using high-throughput literature analysis.

Spyros N Deftereos1, Christos Andronis, Ellen J Friedla

  • 1Biovista Inc., Charlottesville, VA, USA. s.deftereos@biovista.com

Wiley Interdisciplinary Reviews. Systems Biology and Medicine
|March 19, 2011
PubMed
Summary
This summary is machine-generated.

Drug repurposing uses existing medications for new conditions, reducing costs and development time. This approach also aids in predicting adverse drug events by analyzing mechanisms of action via biomedical literature.

More Related Videos

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization
03:08

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization

Published on: October 3, 2025

Related Experiment Videos

Last Updated: Jun 3, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization
03:08

Using Human Differentially Expressed Gene Lists to Perform Downstream Pathway Enrichment Analysis and Target Prioritization

Published on: October 3, 2025

Area of Science:

  • Biomedical Informatics
  • Pharmacology
  • Drug Discovery

Background:

  • Traditional drug development faces rising costs and a scarcity of new chemical entities.
  • Drug repurposing offers a cost-effective and time-efficient alternative by utilizing existing drugs.
  • Existing drug knowledge can be leveraged for predicting adverse events of known or novel drugs.

Purpose of the Study:

  • To review literature-based approaches for drug repurposing.
  • To explore methods for predicting adverse drug events using biomedical literature.
  • To highlight the value of analyzing indirect relationships within biomedical data.

Main Methods:

  • Literature analysis to identify indirect relationships among genes, pathways, and diseases.
  • Network-based approaches to uncover molecular mechanisms of diseases and drug effects.
  • In silico analysis of drug mechanisms of action compared to adverse event mechanisms.

Main Results:

  • Biomedical literature analysis can reveal novel drug indications.
  • Network analysis aids in understanding drug effects and benefit/risk profiles.
  • This approach facilitates the prediction of potential adverse drug events.

Conclusions:

  • Literature-driven drug repurposing and adverse event prediction are valuable strategies.
  • Analyzing complex biomedical networks enhances understanding of drug actions and safety.
  • In silico findings require validation through experimental and clinical studies.