USP39 attenuates the antitumor activity of cisplatin on colon cancer cells dependent on p53
Author:
Funder
National Natural Science Foundation of China
Publisher
Springer Science and Business Media LLC
Subject
Health, Toxicology and Mutagenesis,Cell Biology,Toxicology
Link
https://link.springer.com/content/pdf/10.1007/s10565-021-09683-0.pdf
Reference37 articles.
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2. Branch P, Masson M, Aquilina G, Bignami M, Karran P. Spontaneous development of drug resistance: mismatch repair and p53 defects in resistance to cisplatin in human tumor cells. Oncogene. 2000;19(28):3138–45. https://doi.org/10.1038/sj.onc.1203668.
3. Cepeda V, Fuertes MA, Castilla J, Alonso C, Quevedo C, Pérez JM. Biochemical mechanisms of cisplatin cytotoxicity. Anticancer Agents Med Chem. 2007;7(1):3–18. https://doi.org/10.2174/187152007779314044.
4. Ciombor KK, Bekaii-Saab T. A comprehensive review of sequencing and combination strategies of targeted agents in metastatic colorectal cancer. Oncologist. 2018;23(1):25–34. https://doi.org/10.1634/theoncologist.2017-0203.
5. Dasari S, Tchounwou PB. Cisplatin in cancer therapy: molecular mechanisms of action. Eur J Pharmacol. 2014;5(740):364–78. https://doi.org/10.1016/j.ejphar.2014.07.025.
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