Exploring potential therapeutic combinations for castration-sensitive prostate cancer using supercomputers: a proof of concept study

被引:1
|
作者
Tomic, Drasko [2 ]
Murgic, Jure [1 ]
Frobe, Ana [1 ]
Skala, Karolj [2 ]
Vrljicak, Antonela [1 ]
Rogina, Branka Medved [2 ]
Kolarek, Branimir [2 ]
Bojovic, Viktor [2 ]
机构
[1] Sisters Charity Hosp, Dept Oncol & Nucl Med, Zagreb 10000, Croatia
[2] Rudjer Boskovic Inst, Ctr Informat & Comp, Zagreb 10000, Croatia
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
DRUG; CHAIN; PREDICTION; DOCKING; NETWORK;
D O I
10.1038/s41598-024-69880-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To address the challenge of finding new combination therapies against castration-sensitive prostate cancer, we introduce Vini, a computational tool that predicts the efficacy of drug combinations at the intracellular level by integrating data from the KEGG, DrugBank, Pubchem, Protein Data Bank, Uniprot, NCI-60 and COSMIC databases. Vini is a computational tool that predicts the efficacy of drugs and their combinations at the intracellular level. It addresses the problem comprehensively by considering all known target genes, proteins and small molecules and their mutual interactions involved in the onset and development of cancer. The results obtained point to new, previously unexplored combination therapies that could theoretically be promising candidates for the treatment of castration-sensitive prostate cancer and could prevent the inevitable progression of the cancer to the incurable castration-resistant stage. Furthermore, after analyzing the obtained triple combinations of drugs and their targets, the most common targets became clear: ALK, BCL-2, mTOR, DNA and androgen axis. These results may help to define future therapies against castration-sensitive prostate cancer. The use of the Vini computer model to explore therapeutic combinations represents an innovative approach in the search for effective treatments for castration-sensitive prostate cancer, which, if clinically validated, could potentially lead to new breakthrough therapies.
引用
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页数:11
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