| RRC ID |
56627
|
| 著者 |
Tanaka M, Zhu Y, Shionyu M, Ota N, Shibata N, Watanabe C, Mizusawa A, Sasaki R, Mizukami T, Shiina I, Hasegawa M.
|
| タイトル |
Ridaifen-F conjugated with cell-penetrating peptides inhibits intracellular proteasome activities and induces drug-resistant cell death.
|
| ジャーナル |
Eur J Med Chem
|
| Abstract |
Ridaifen-F (RID-F) potently inhibits proteolytic activities of the 20S proteasome but poorly inhibits those of the 26S proteasome. Here, we report preparation of several conjugates in which various peptides are connected to RID-F. Conjugates with peptides consisting of seven amino acid residues significantly inhibited the 26S proteasome. Particularly, RID-F conjugated to an octaarginine peptide (R8, a so-called cell-penetrating peptide) inhibited intracellular proteasome activities and induced cell death in drug-resistant KMS-11 myeloma cells. RID-F conjugated to hydrophobic peptides also inhibited the 26S proteasome but failed to induce cell death, suggesting poor penetration into cells. We infer that the R8 peptide has dual functions: (1) rapid penetration of conjugates into the cell increases intracellular drug concentrations sufficient for exhibition of its effect, and (2) recognition of the conjugates by the 26S proteasome stimulates drug entry into the catalytic chamber. In the presence of ATPγS, RID-F conjugates containing R8 inhibited the 26S proteasome more potently than in the presence of ATP, suggesting efficient entry of drugs into the catalytic chamber in a similar fashion to the substrate. Taken together with docking simulations of RID-F conjugate interactions with proteasome active sites, the second function of R8 peptide is plausible. Thus, the conjugation of nonpeptidic proteasome inhibitors to a cell-penetrating peptide could represent a viable strategy for overcoming the drug-resistance of tumor cells.
|
| 巻・号 |
146
|
| ページ |
636-650
|
| 公開日 |
2018-2-25
|
| DOI |
10.1016/j.ejmech.2018.01.045
|
| PII |
S0223-5234(18)30058-8
|
| PMID |
29407987
|
| MeSH |
Antineoplastic Agents / chemical synthesis
Antineoplastic Agents / chemistry
Antineoplastic Agents / pharmacology*
Cell Death / drug effects
Cell Proliferation / drug effects
Cell-Penetrating Peptides / chemistry
Cell-Penetrating Peptides / pharmacology*
Dose-Response Relationship, Drug
Drug Resistance, Neoplasm / drug effects*
Drug Screening Assays, Antitumor
Humans
Molecular Structure
Proteasome Endopeptidase Complex / metabolism*
Proteasome Inhibitors / chemistry
Proteasome Inhibitors / pharmacology*
Structure-Activity Relationship
Tamoxifen / analogs & derivatives*
Tamoxifen / chemistry
Tamoxifen / pharmacology
Tumor Cells, Cultured
|
| IF |
4.833
|
| 引用数 |
3
|
| リソース情報 |
| ヒト・動物細胞 |
RPMI8226(RCB3010) |
