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- W4387296867 abstract "To explore the regulatory networks that underlie the development of chemoresistance in bladder cancer, we analyzed profiles of differentially expressed lncRNAs, circRNAs, miRNAs and mRNAs in gemcitabine-resistant/sensitive bladder cancer cells using next-generation sequencing data. Hundreds of differentially expressed lncRNAs and miRNAs and thousands of circRNAs and mRNAs were identified. Bioinformatics analysis revealed the chromosomal localizations, classification, and coexpression of mRNAs, as well as candidates for cis and trans regulation by lncRNAs. Furthermore, GO and KEGG pathway enrichment analysis of differentially expressed mRNAs and circRNAs indicated important functional roles of co-regulated RNAs, thus establishing ceRNA and protein-protein interactions networks that may underlie chemoresistance in bladder cancer. We demonstrated that lncRNA LINP1 can act as a ceRNA by inhibiting miR-193a-5p to increase TP73 expression; and that lncRNA ESRG and hsa_circ_0075881 can simultaneously bind miR-324-3p to increase ST6GAL1 expression. Modulation of ceRNA network components using ablation and overexpression approaches contributed to gemcitabine resistance in bladder cancer cells. These results elucidate mechanisms by which lncRNAs and circRNAs coregulate the development of bladder cancer cell resistance to gemcitabine, thus laying the foundation for future research to identify biomarkers and disease targets." @default.
- W4387296867 created "2023-10-04" @default.
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- W4387296867 date "2023-10-03" @default.
- W4387296867 modified "2023-10-04" @default.
- W4387296867 title "Construction and identification of lncRNA/circRNA coregulated ceRNA networks in gemcitabine-resistant bladder carcinoma" @default.
- W4387296867 doi "https://doi.org/10.1093/carcin/bgad065" @default.
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- W4387296867 hasPublicationYear "2023" @default.
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