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A Strategy Utilizing Protein–Protein Interaction Hubs for the Treatment of Cancer Diseases.

Authors :
Carels, Nicolas
Sgariglia, Domenico
Junior, Marcos Guilherme Vieira
Lima, Carlyle Ribeiro
Carneiro, Flávia Raquel Gonçalves
Silva, Gilberto Ferreira da
Silva, Fabricio Alves Barbosa da
Scardini, Rafaela
Tuszynski, Jack Adam
Andrade, Cecilia Vianna de
Monteiro, Ana Carolina
Martins, Marcel Guimarães
Silva, Talita Goulart da
Ferraz, Helen
Finotelli, Priscilla Vanessa
Balbino, Tiago Albertini
Pinto, José Carlos
Source :
International Journal of Molecular Sciences. Nov2023, Vol. 24 Issue 22, p16098. 29p.
Publication Year :
2023

Abstract

We describe a strategy for the development of a rational approach of neoplastic disease therapy based on the demonstration that scale-free networks are susceptible to specific attacks directed against its connective hubs. This strategy involves the (i) selection of up-regulated hubs of connectivity in the tumors interactome, (ii) drug repurposing of these hubs, (iii) RNA silencing of non-druggable hubs, (iv) in vitro hub validation, (v) tumor-on-a-chip, (vi) in vivo validation, and (vii) clinical trial. Hubs are protein targets that are assessed as targets for rational therapy of cancer in the context of personalized oncology. We confirmed the existence of a negative correlation between malignant cell aggressivity and the target number needed for specific drugs or RNA interference (RNAi) to maximize the benefit to the patient's overall survival. Interestingly, we found that some additional proteins not generally targeted by drug treatments might justify the addition of inhibitors designed against them in order to improve therapeutic outcomes. However, many proteins are not druggable, or the available pharmacopeia for these targets is limited, which justifies a therapy based on encapsulated RNAi. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
24
Issue :
22
Database :
Academic Search Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
173832245
Full Text :
https://doi.org/10.3390/ijms242216098