Bioinformatics and In silico approaches to identify novel biomarkers and key pathways for cancers that are linked to the progression of female infertility: A comprehensive approach for drug discovery

被引:4
作者
Hossain, Md. Arju [1 ]
Sohel, Md [2 ]
Rahman, Md Habibur [3 ]
Hasan, Md Imran [3 ]
Khan, Md. Sharif [1 ]
Amin, Md. Al [1 ]
Islam, Md. Zahidul [4 ]
Peng, Silong [5 ]
机构
[1] Mawlana Bhashani Sci & Technol Univ, Dept Biotechnol & Genet Engn, Tangail, Bangladesh
[2] Mawlana Bhashani Sci & Technol Univ, Dept Biochem & Mol Biol, Tangail, Bangladesh
[3] Islamic Univ, Dept Comp Sci & Engn, Kushtia, Bangladesh
[4] Nagoya Univ, Grad Sch Engn, Dept Elect, Nagoya, Japan
[5] Univ Chinese Acad Sci, Inst Automat, Chinese Acad Sci, Beijing, Peoples R China
来源
PLOS ONE | 2023年 / 18卷 / 01期
关键词
REGULATORY SUBUNIT P85-ALPHA; GENE-EXPRESSION ANALYSIS; CELL-PROLIFERATION; MUTATIONS; DISEASE; GROWTH; VEGF; COMORBIDITIES; ACTIVATION; MECHANISMS;
D O I
10.1371/journal.pone.0265746
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
Despite modern treatment, infertility remains one of the most common gynecologic diseases causing severe health effects worldwide. The clinical and epidemiological data have shown that several cancerous risk factors are strongly linked to Female Infertility (FI) development, but the exact causes remain unknown. Understanding how these risk factors affect FI-affected cell pathways might pave the door for the discovery of critical signaling pathways and hub proteins that may be targeted for therapeutic intervention. To deal with this, we have used a bioinformatics pipeline to build a transcriptome study of FI with four carcinogenic risk factors: Endometrial Cancer (EC), Ovarian Cancer (OC), Cervical Cancer (CC), and Thyroid Cancer (TC). We identified FI sharing 97, 211, 87 and 33 differentially expressed genes (DEGs) with EC, OC, CC, and TC, respectively. We have built gene-disease association networks from the identified genes based on the multilayer network and neighbour-based benchmarking. Identified TNF signalling pathways, ovarian infertility genes, cholesterol metabolic process, and cellular response to cytokine stimulus were significant molecular and GO pathways, both of which improved our understanding the fundamental molecular mechanisms of cancers associated with FI progression. For therapeutic intervention, we have targeted the two most significant hub proteins VEGFA and PIK3R1, out of ten proteins based on Maximal Clique Centrality (MCC) value of cytoscape and literature analysis for molecular docking with 27 phytoestrogenic compounds. Among them, sesamin, galangin and coumestrol showed the highest binding affinity for VEGFA and PIK3R1 proteins together with favourable ADMET properties. We recommended that our identified pathway, hub proteins and phytocompounds may be served as new targets and therapeutic interventions for accurate diagnosis and treatment of multiple diseases.
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页数:28
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