AS602801, an Anticancer Stem Cell Candidate Drug, Reduces Survivin Expression and Sensitizes A2780 Ovarian Cancer Stem Cells to Carboplatin and Paclitaxel

被引:16
作者
Yamamoto, Masahiro [1 ]
Suzuki, Shuhei [1 ,2 ]
Togashi, Keita [1 ,3 ]
Sanomachi, Tomomi [1 ,2 ]
Seino, Shizuka [1 ]
Kitanaka, Chifumi [1 ,4 ]
Okada, Masashi [1 ]
机构
[1] Yamagata Univ, Sch Med, Dept Mol Canc Sci, Yamagata 9909585, Japan
[2] Yamagata Univ, Sch Med, Dept Clin Oncol, Yamagata, Japan
[3] Yamagata Univ, Sch Med, Dept Ophthalmol, Yamagata, Japan
[4] Yamagata Univ, Res Inst Promot Med Sci, Fac Med, Yamagata, Japan
关键词
Drug repositioning; repurposing; drug resistance; SELF-RENEWAL; INHIBITOR; CARCINOMA; APOPTOSIS; CAPACITY; THERAPY; TARGETS; GROWTH; DEATH;
D O I
10.21873/anticanres.13038
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: AS602801, a novel inhibitor of c-Jun N-terminal kinase (JNK), suppresses tumor initiation capacity and metastatic potential of cancer stem cells (CSCs). However, it remains unknown whether this inhibitor can chemosensitize CSCs. Materials and Methods: Using A2780 CSLC, a CSC line derived from ovarian cancer, this study examined the combinational effects of AS602801 and carboplatin or paclitaxel and explored the mechanism of those effects. Results: AS602801 chemosensitized A2780 CSLC cells to carboplatin and paclitaxel. With respect to the mechanism of chemosensitization, the expression of survivin, an anti-apoptotic protein, was reduced by AS602801. Pharmacological and genetic inhibition of survivin chemosensitized the cells to carboplatin and paclitaxel. Suppression of survivin by AS602801 was also observed in other types of CSCs and nonCSCs. Conclusion: AS602801, which reduces survivin expression, can chemosensitize ovarian CSCs and is a candidate drug that targets the chemoresistance, tumor initiating capacity and metastasis of CSCs.
引用
收藏
页码:6699 / 6706
页数:8
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