Wibowo, Moh Arikus and Nugroho, Eri Prasetyo and Hermawan, Adam (2021) Genomic Understanding Reveals the Important Role of FGFR2 as Paeoniflorin Target for Circumventing Breast Cancer Resistance to Tamoxifen. Asian Pacific Journal of Cancer Prevention, 22 (12). 3949 – 3958. ISSN 15137368
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Objectives: Paeoniflorin (PF), a compound found in Paeonia lactiflora and Paeonia suffruticosa, has anticancer potential, particularly in inhibiting migration and invasion, the resistant cancer cells hallmarks. To date, the mechanismof overcoming tamoxifen resistance in breast cancer is not yet elucidated. This research aims to explore the potentialtarget of PF as a co-treatment for circumventing breast cancer resistance to tamoxifen with a genomic understandingbioinformatics.Methods: Microarray data originating from GSE67916 and GSE85871 in the NCBI GEO database wasanalyzed to obtain differentially expressed genes (DEGs). Further analyses were performed on DEGs using the DAVIDv6.8, STRING-DB v11.0, the Cytoscape, and cBioportal. Gene expression analysis validation in breast cancer cellsand tamoxifen-resistant breast cancer cells was accomplished using GEPIA and ONCOMINE databases. Survival rateanalysis of selected genes was conducted using Kaplan–Meier. Results: We obtained 175 DEGs from the two samples(tamoxifen-resistant and paeoniflorin-treated). DEG involves in 70 biological processes, 26 cellular components, and18 molecular functions, and three pathways relevant to breast cancer. The PPI network analysis and hub genes selectionobtained 10 genes with the highest degree scores. Genetic changes for selected genes, including IFNB1, CDK6, FGFR2,OAS1, BCL2, and STAT2 were found from 0.5 to 7 of the case population per patient case. Additional analysis usingcBioportal revealed FGFR signaling pathway through Ras is important for the PF mechanism in circumventing breastcancer resistance to tamoxifen. ONCOMINE and GEPIA analysis emphasized the importance of selected genes in thetamoxifen-resistance mechanism. Conclusion: PF has potential to be used as a co-treatment for circumventing breastcancer resistance to tamoxifen by targeting FGFR2 signaling, but further validation is needed © This work is licensed under a Creative Commons Attribution-Non Commercial 4.0 International License
Item Type: | Article |
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Additional Information: | Cited by: 1; All Open Access, Gold Open Access, Green Open Access |
Uncontrolled Keywords: | Antineoplastic Agents; Breast Neoplasms; Computational Biology; Databases, Genetic; Drug Resistance, Neoplasm; Female; Gene Expression Regulation, Neoplastic; Gene Regulatory Networks; Genomics; Glucosides; Humans; Kaplan-Meier Estimate; Monoterpenes; Protein Interaction Maps; Receptor, Fibroblast Growth Factor, Type 2; Signal Transduction; Tamoxifen; antineoplastic agent; FGFR2 protein, human; fibroblast growth factor receptor 2; glucoside; paeoniflorin; tamoxifen; terpene; biology; breast tumor; drug effect; drug resistance; female; gene expression regulation; gene regulatory network; genetic database; genetics; genomics; human; Kaplan Meier method; protein analysis; signal transduction |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Divisions: | Faculty of Pharmacy |
Depositing User: | Sri JUNANDI |
Date Deposited: | 20 Sep 2024 06:26 |
Last Modified: | 20 Sep 2024 06:26 |
URI: | https://ir.lib.ugm.ac.id/id/eprint/4798 |