{"title":"The use of different types of networks, alone and in combination, for drug target identification.","authors":"Paolo Parini","doi":"10.1111/bph.70091","DOIUrl":null,"url":null,"abstract":"<p><p>Current therapeutic approaches often focus on targeting clinical symptoms or peripheral phenotypes rather than the underlying molecular mechanisms, or endophenotypes, that drive diseases. While symptom-based drugs can alleviate discomfort, they do not necessarily alter disease progression and may overlook opportunities for prevention or early intervention in asymptomatic patients. This approach can lead to overtreatment of certain disease traits while neglecting others that are critical for long-term outcomes. In contrast, mechanism-based therapies offer advantages such as specificity and reduced side effects, allowing for the management of previously untreatable conditions or complementing established treatments. These therapies enable monitoring of drug effects on the endophenotype driving the disease, facilitating personalised treatment regimens and improving patient compliance. Mechanism-based drugs are essential for precision prevention and therapy. Network Medicine plays a vital role in understanding diseases by identifying key endophenotypes and determinants influencing disease expression. Unlike reductionist methods, it provides insights into disease mechanisms and potential therapeutic targets by examining interactions among genetic, molecular and environmental factors. As part of Network Medicine, Network Pharmacology bridges the gap between symptom-based and mechanism-based strategies, guiding drug development while considering symptomatic relief. This short review focus on creating heterogeneous networks to integrate various drug, target and disease-related information. These approaches can create comprehensive representations of drugs and targets by incorporating diverse profiles, enhancing the prediction performance of drug target interactions.</p>","PeriodicalId":9262,"journal":{"name":"British Journal of Pharmacology","volume":" ","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"British Journal of Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/bph.70091","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Current therapeutic approaches often focus on targeting clinical symptoms or peripheral phenotypes rather than the underlying molecular mechanisms, or endophenotypes, that drive diseases. While symptom-based drugs can alleviate discomfort, they do not necessarily alter disease progression and may overlook opportunities for prevention or early intervention in asymptomatic patients. This approach can lead to overtreatment of certain disease traits while neglecting others that are critical for long-term outcomes. In contrast, mechanism-based therapies offer advantages such as specificity and reduced side effects, allowing for the management of previously untreatable conditions or complementing established treatments. These therapies enable monitoring of drug effects on the endophenotype driving the disease, facilitating personalised treatment regimens and improving patient compliance. Mechanism-based drugs are essential for precision prevention and therapy. Network Medicine plays a vital role in understanding diseases by identifying key endophenotypes and determinants influencing disease expression. Unlike reductionist methods, it provides insights into disease mechanisms and potential therapeutic targets by examining interactions among genetic, molecular and environmental factors. As part of Network Medicine, Network Pharmacology bridges the gap between symptom-based and mechanism-based strategies, guiding drug development while considering symptomatic relief. This short review focus on creating heterogeneous networks to integrate various drug, target and disease-related information. These approaches can create comprehensive representations of drugs and targets by incorporating diverse profiles, enhancing the prediction performance of drug target interactions.
期刊介绍:
The British Journal of Pharmacology (BJP) is a biomedical science journal offering comprehensive international coverage of experimental and translational pharmacology. It publishes original research, authoritative reviews, mini reviews, systematic reviews, meta-analyses, databases, letters to the Editor, and commentaries.
Review articles, databases, systematic reviews, and meta-analyses are typically commissioned, but unsolicited contributions are also considered, either as standalone papers or part of themed issues.
In addition to basic science research, BJP features translational pharmacology research, including proof-of-concept and early mechanistic studies in humans. While it generally does not publish first-in-man phase I studies or phase IIb, III, or IV studies, exceptions may be made under certain circumstances, particularly if results are combined with preclinical studies.