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논문 기본 정보

자료유형
학술저널
저자정보
Wang Jiamin (Sichuan University China) Liu Lixia (Northwest Minzu University China) Yang Di (Northwest Minzu University China) Zhang Li (Northwest Minzu University China) Abudureyimu Ayimuguli (Northwest Minzu University China) Qiao Zilin (Northwest Minzu University China) Ma Zhongren (Sichuan University China)
저널정보
한국유전학회 Genes & Genomics Genes & Genomics Vol.44 No.2
발행연도
2022.2
수록면
187 - 196 (10page)
DOI
10.1007/s13258-021-01177-x

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Background Madin–Darby canine kidney (MDCK) cells are widely used for vaccine production, however, the safety of MDCK cells needs to be considered seriously because of high tumorigenicity. Micro RNAs (miRNAs) that are involved in the tumorigenicity of MDCK cells have been never been reported. Objective To reveal the role of miRNA in the tumorigenic phenotype of MDCK cell line. Methods The miRNA expression profiles of two monoclonal MDCK cells (M09CL and M35CL) with low tumorigenicity and one MDCK cell line (M73P) with high tumorigenicity were characterized and investigated by using small RNA-seq technology. Results A total of 5 known miRNAs and 5 novel miRNAs were highly expressed in M73P. In addition, 4 known miRNAs and 4 novel miRNAs were highly expressed in M09CL and M35CL. The target genes of the differentially expressed miRNAs were significantly enriched in several biological processes, and the majority of these genes were involved in pathways in cancer and the MAPK signaling pathway. Through interaction analysis, 4 up-regulated miRNAs (cfa-miR-452, cfa-miR-8826, cfa-miR-224, and cfa-miR-2387) and their crucial target genes related to the tumor regulation network were identified. Results indicated these 4 miRNAs might play crucial roles in the tumorigenesis of MDCK cells. Conclusion Our findings, which were based on the functional prediction of miRNAs and target genes, suggested that miRNAs might influence the tumorigenicity of MDCK cells by regulating target genes. Moreover, the results provided important data for understanding the miRNA-mediated regulatory networks that control the tumorigenicities of MDCK cells.

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