序号38
伊立替康
顺铂
喜树碱
流式细胞术
细胞毒性
细胞凋亡
活性代谢物
细胞周期
癌症研究
药理学
化疗
化学
癌症
生物
医学
体外
内科学
分子生物学
生物化学
结直肠癌
药代动力学
作者
Nagio Takigawa,Masako Takeyama,Takuo Shibayama,Atsuhiko Tada,Noriko Kawata,Chiharu Okada,Keisuke Aoe,Toshiyuki Kozuki,Katsuyuki Hotta,Masahiro Tabata,Katsuyuki Kiura,Hiroshi Ueoka,Mitsune Tanimoto,Kiyoshi Takahashi
摘要
The single agent of amrubicin is active in untreated small-cell lung cancer (SCLC). Cytotoxicity of amrubicinol, the active form of amrubicin, was evaluated in a parent SCLC cell line (SBC-3); an active metabolite of irinotecan, 7-ethyl-10-hydroxy-camptothecin (SN-38)-resistant subline (SBC-3/SN-38); and cisplatin-resistant subline (SBC-3/CDDP) using AlamarBlue assay. Interaction of the combined drugs was evaluated by median-effect plot analysis, and the fraction of apoptotic cells was determined using flow cytometry. SBC-3/SN-38 was 34-fold more resistant to SN-38 and SBC-3/CDDP was 7.2-fold more resistant to cisplatin than parental SBC-3. However, these resistant sublines retained sensitivity to amrubicinol (1.8- and 1.7-fold, respectively). Simultaneous exposure of SBC-3/SN-38 cells to amrubicinol and cisplatin showed a synergistic effect. Simultaneous exposure of SBC-3/CDDP cells to amrubicinol and SN-38 displayed synergistic or additive effects. The two-drug combination produced an increase of apoptotic cells compared to each single agent alone in both resistant cells. These findings suggest that amrubicin alone and in combination with cisplatin or irinotecan is effective against SCLC refractory to irinotecan and/or cisplatin.
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