Title : MicroRNA‑10b modulates cisplatin tolerance by targeting p53 directly in lung cancer cells.

Pub. Date : 2021 Aug

PMID : 34165168






7 Functional Relationships(s)
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1 MicroRNA-10b modulates cisplatin tolerance by targeting p53 directly in lung cancer cells. Cisplatin tumor protein p53 Homo sapiens
2 In functional assays, upregulation of the p53 signaling pathway following cisplatin treatment was associated with decreased levels of miR-10b and upregulation of the luciferase activity of wild-type, but not 1,584, 2,032-dual-mutant, p53 3"-UTR. Cisplatin tumor protein p53 Homo sapiens
3 The ectopic expression of miR-10b-agomir attenuated the stability of p53 3"-UTR and the expression of p53 and its downstream effectors induced by cisplatin. Cisplatin tumor protein p53 Homo sapiens
4 The ectopic expression of miR-10b-agomir attenuated the stability of p53 3"-UTR and the expression of p53 and its downstream effectors induced by cisplatin. Cisplatin tumor protein p53 Homo sapiens
5 By contrast, the knockdown of miR-10b induced the stability of p53 3"-UTR and increased levels of p53 and the sensitivity of A549 cells to cisplatin treatment. Cisplatin tumor protein p53 Homo sapiens
6 By contrast, the knockdown of miR-10b induced the stability of p53 3"-UTR and increased levels of p53 and the sensitivity of A549 cells to cisplatin treatment. Cisplatin tumor protein p53 Homo sapiens
7 These findings indicate a novel pathway in which cisplatin induces the levels of p53 by increasing mRNA stability via miR-10b, indicating a novel oncogenic role of miR-10b in promoting the malignant characteristics of non-small cell lung carcinoma. Cisplatin tumor protein p53 Homo sapiens