Discovering Innovative Drugs Targeting Both Cancer and Cardiovascular Disease by Shared Protein-Protein Interaction Network Analyses

被引:8
|
作者
Tiwari, Sameeksha [1 ]
Dwivedi, Upendra N. [1 ,2 ]
机构
[1] Univ Lucknow, Bioinformat Infrastruct Facil, Dept Biochem, Ctr Excellence Bioinformat, Lucknow 226007, Uttar Pradesh, India
[2] Univ Lucknow, Inst Dev Adv Comp, ONGC Ctr Adv Studies, Lucknow, Uttar Pradesh, India
关键词
drug discovery; cancer; cardiology; protein-protein interaction; computational biology; drug targets; BREAST-CANCER; TOPOLOGICAL FEATURES; RISK-FACTORS; IN-VIVO; BRCA1; P53; RAD51; GENE; BINDING; OBESITY;
D O I
10.1089/omi.2019.0095
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cancer and cardiovascular disease (CVD) have a common co-occurrence. Both diseases display overlapping pathophysiology and risk factors, suggesting shared biological mechanisms. Conditions such as obesity, diabetes, hypertension, smoking, poor diet, and inadequate physical activity can cause both heart disease and cancer. The burgeoning field of onco-cardiology aims to develop diagnostics and innovative therapeutics for both diseases through targeting shared mechanisms and molecular targets. In this overarching context, this expert review presents an analysis of the protein-protein interaction (PPI) networks for onco-cardiology drug discovery. Several PPI complexes such as MDM2-TP53 and CDK4-pRB have been studied for their tumor-suppressive functions. In addition, XIAP-SMAC, RAC1-GEF, Sur-2ESX, and TP53-BRCA1 are other PPI complexes that offer potential breakthrough for onco-cardiology therapeutics innovation. As both cancer and CVD share biological mechanisms to a certain degree, the PPI network analyses for onco-cardiology drug discovery are promising for addressing comorbid diseases in the spirit of systems medicine. We discuss the emerging architecture of PPI networks in cancer and CVD and prospects and challenges for their exploitation toward therapeutics applications. Finally, we emphasize that PPIs that were once thought to be undruggable have become potential new class of innovative drug targets.
引用
收藏
页码:417 / 425
页数:9
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