論文 - 詳細
| RRC ID | 77504 |
|---|---|
| 著者 | Yoshida K, Fujita A, Narazaki H, Asano T, Itoh Y. |
| タイトル | Drug resistance to nelarabine in leukemia cell lines might be caused by reduced expression of deoxycytidine kinase through epigenetic mechanisms. |
| ジャーナル | Cancer Chemother Pharmacol |
| Abstract |
PURPOSE:Drug resistance is a serious problem in leukemia therapy. A novel purine nucleoside analogue, nelarabine, is available for the treatment of children with T cell acute lymphoblastic leukemia. We investigated the mechanisms of drug resistance to nelarabine. METHODS:Nelarabine-resistant cells were selected by stepwise and continuous exposure to nelarabine using the limiting dilution method in human B and T cell lymphoblastic leukemia cell lines. Expression analysis was performed using real-time polymerase chain reaction, and epigenetic analysis was performed using methylation-specific polymerase chain reaction and chromatin immunoprecipitation. RESULTS:The RNA expression level for deoxycytidine kinase (dCK) was decreased in nelarabine-resistant leukemia cells. There were no differences between the parental and nelarabine-resistant leukemia cells in the methylation status of the promoter region of the dCK gene. In the chromatin immune precipitation assay, decreased acetylation of histones H3 and H4 bound to the dCK promoter was seen in the nelarabine-resistant cells when compared to the parental cells. Furthermore, treatment with a novel histone deacetylase inhibitor, vorinostat, promoted the cytotoxic effect of nelarabine along with increased expression of the dCK gene, and it increased acetylation of both histones H3 and H4 bound to the dCK promoter in nelarabine-resistant leukemia cells. The combination index showed that the effect of nelarabine and vorinostat was synergistic. CONCLUSION:This study reports that nelarabine with vorinostat can promote cytotoxicity in nelarabine-resistant leukemia cells through epigenetic mechanisms. |
| 巻・号 | 89(1) |
| ページ | 83-91 |
| 公開日 | 2022-1-1 |
| DOI | 10.1007/s00280-021-04373-4 |
| PII | 10.1007/s00280-021-04373-4 |
| PMID | 34825941 |
| MeSH | Acetylation Antineoplastic Agents / pharmacology* Arabinonucleosides / pharmacology* Cell Line, Tumor CpG Islands DNA Methylation Deoxycytidine Kinase / genetics* Deoxycytidine Kinase / metabolism Drug Resistance, Neoplasm / drug effects Drug Resistance, Neoplasm / genetics* Epigenesis, Genetic / drug effects Gene Expression Regulation, Leukemic / drug effects Histone Deacetylase Inhibitors / pharmacology Histones / genetics Histones / metabolism Humans Precursor Cell Lymphoblastic Leukemia-Lymphoma / drug therapy* Precursor Cell Lymphoblastic Leukemia-Lymphoma / genetics Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology Promoter Regions, Genetic Vorinostat / pharmacology |
| IF | 2.967 |
| リソース情報 | |
| ヒト・動物細胞 | MOLT-4(RCB0206) SKW-3(RCB1168) |