Novitasari, Dhania and Jenie, Riris Istighfari and Kato, Jun-ya and Meiyanto, Edy (2021) The integrative bioinformatic analysis deciphers the predicted molecular target gene and pathway from curcumin derivative CCA-1.1 against triple-negative breast cancer (TNBC). Journal of the Egyptian National Cancer Institute, 33 (1). ISSN 11100362
Full text not available from this repository. (Request a copy)Abstract
Background: The poor outcomes from triple-negative breast cancer (TNBC) therapy are mainly because of TNBC cells’ heterogeneity, and chemotherapy is the current approach in TNBC treatment. A previous study reported that CCA-1.1, the alcohol-derivative from monocarbonyl PGV-1, exhibits anticancer activities against several cancer cells, as well as in TNBC. This time, we utilized an integrative bioinformatics approach to identify potential biomarkers and molecular mechanisms of CCA-1.1 in inhibiting proliferation in TNBC cells. Methods: Genomics data expression were collected through UALCAN, derived initially from TCGA-BRCA data, and selected for TNBC-only cases. We predict CCA-1.1 potential targets using SMILES-based similarity functions across six public web tools (BindingDB, DINIES, Swiss Target Prediction, Polypharmacology browser/PPB, Similarity Ensemble Approach/SEA, and TargetNet). The overlapping genes between the CCA-1.1 target and TNBC (CPTGs) were selected and used in further assessment. Gene ontology (GO) enrichment and the Kyoto Encyclopedia of Genes and Genomes (KEGG) network analysis were generated in WebGestalt. The protein–protein interaction (PPI) network was established in STRING-DB, and then the hub-genes were defined through Cytoscape. The hub-gene’s survival analysis was processed via CTGS web tools using TCGA database. Results: KEGG pathway analysis pointed to cell cycle process which enriched in CCA-1.1 potential targets. We also identified nine CPTGs that are responsible in mitosis, including AURKB, PLK1, CDK1, TPX2, AURKA, KIF11, CDC7, CHEK1, and CDC25B. Conclusion: We suggested CCA-1.1 possibly regulated cell cycle process during mitosis, which led to cell death. These findings needed to be investigated through experimental studies to reinforce scientific data of CCA-1.1 therapy against TNBC. © 2021, The Author(s).
Item Type: | Article |
---|---|
Additional Information: | Cited by: 9; All Open Access, Gold Open Access |
Uncontrolled Keywords: | Cell Cycle Proteins; Computational Biology; Curcumin; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Humans; Protein-Serine-Threonine Kinases; Triple Negative Breast Neoplasms; antineoplastic agent; aurora A kinase; aurora B kinase; biological marker; cca 1.1; cca 11; cell division cycle 7 kinase; checkpoint kinase 1; curcumin; cyclin dependent kinase 1; kinesin; kinesin family member 11; M phase inducer phosphatase 2; phosphatase; phosphotransferase; polo like kinase 1; targeting protein for xklp2; unclassified drug; CDC7 protein, human; cell cycle protein; curcumin; protein serine threonine kinase; Article; bioinformatics; cancer chemotherapy; cell cycle; cell cycle regulation; controlled study; disease free survival; down regulation; drug mechanism; drug protein binding; drug structure; drug targeting; female; gene expression; gene ontology; human; human cell; human tissue; mitosis; overall survival; overlapping gene; polypharmacology; protein protein interaction; survival analysis; triple negative breast cancer; upregulation; biology; gene expression profiling; gene expression regulation; genetics; triple negative breast cancer |
Subjects: | R Medicine > RS Pharmacy and materia medica |
Divisions: | Faculty of Pharmacy |
Depositing User: | Sri JUNANDI |
Date Deposited: | 27 Sep 2024 03:50 |
Last Modified: | 27 Sep 2024 03:50 |
URI: | https://ir.lib.ugm.ac.id/id/eprint/4537 |