SET and MYND domain-containing protein 3 inhibits tumor cell sensitivity to cisplatin
Autor: | Xiao‑Ying Chen, Man‑Li Xu, Tong-Cun Zhang, Qing‑Qing Dong, Hong‑Peng He, Nan Wang, Chang Wang, Lei Wang, Zhi Miao, Xue-Gang Luo |
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Jazyk: | angličtina |
Rok vydání: | 2020 |
Předmět: |
0301 basic medicine
Cisplatin Cancer Research Small interfering RNA Gene knockdown Oncogene Chemistry Cell tumor cells Transfection Articles Cell cycle 03 medical and health sciences 030104 developmental biology 0302 clinical medicine medicine.anatomical_structure Oncology SET and MYND domain containing 3 030220 oncology & carcinogenesis cisplatin sensitivity Cancer research medicine Clonogenic assay medicine.drug |
Zdroj: | Oncology Letters |
ISSN: | 1792-1082 1792-1074 |
Popis: | Cisplatin resistance has been a major factor limiting its clinical use as a chemotherapy drug. The present study aimed to investigate whether SET and MYND domain-containing protein 3 (SMYD3), a histone methyltransferase closely associated with tumors can affect the sensitivity of tumors to cisplatin chemotherapy. Real time-qPCR, western blotting, the luciferase reporter, MTT and clonogenic assays were performed to detect the effects of SMYD3 on the chemotherapy capacity of cisplatin. In the present study, SMYD3 exhibited different expression patterns in MCF-7 and T47D breast cancer cells. In addition, this differential expression was associated with tumor cell resistance to cisplatin. Furthermore, SMYD3 knockdown following small interfering RNA transfection increased cisplatin sensitivity, whereas SMYD3 overexpression decreased cisplatin sensitivity. In addition, SMYD3 knockdown synergistically enhanced cisplatin-induced cell apoptosis. SMYD3 expression was downregulated during cisplatin treatment. In addition, transcriptional regulatory activities of SMYD3 3'-untranslated region were also downregulated. These results suggested that SMYD3 may affect cell sensitivity to cisplatin and participate in the development of cisplatin resistance, which is a process that may involve microRNA-124-mediated regulation. |
Databáze: | OpenAIRE |
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