EventsThe 3rd International Electronic Conference on Applied Sciences
Published
with-doi10.3390/ASEC2022-13847 (registering DOI)
This submission belongs to the session A. Applied Biosciences and Bioengineering of the event The 3rd International Electronic Conference on Applied Sciences
Published date
12 Dec, 2022
Academic Editor
author-avatarRoger Narayan
Citation
Ha Nguyen, Uyen Tu BUI, Gene re-ranking and controllability analysis of protein – protein network for discovery potential drug target of breast cancer at different stages, in Proceedings of The 3rd International Electronic Conference on Applied Sciences, 1 December–15 December 2022, MDPI: Basel, Switzerland, doi: 10.3390/ASEC2022-13847
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Gene re-ranking and controllability analysis of protein – protein network for discovery potential drug target of breast cancer at different stages

Uyen Tu BUI 1
image
1. Hanoi Amsterdam High School for the Gifted
2. Hanoi University of Pharmacy, Vietnam
Abstract

The protein-protein interaction network (PPIN) is essential for functional processing and mechanism of multiple complex diseases. Recently, control theory has applied to protein interaction with the aims of identify the minimum set of nodes that can drive the whole network to the desired state. Here, we use different statistic network inference methods to generate the highest-scored re-ranking gene list as the source for constructing protein-protein interaction network. Then we characterize structural controllability of directed and weighted PPINs for breast cancer stages. The maximum matching approach for controllability analysis allows classifying nodes into three categories: critical, intermittent and redundant. This leads to identifying the most important proteins as critical nodes for each stage of breast cancer. In total, 70 critical nodes as drug targets have been revealed across stages in this study.

Keywords
control theory
breast cancer
drug targets
maximum matching
protein-protein interaction network
critical
intermittent and redundant nodes
Manuscript
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