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Updated: Feb 1, 2026

Enrichment for Chemoresistant Ovarian Cancer Stem Cells from Human Cell Lines
Published on: September 10, 2014
AS602801, an Anticancer Stem Cell Candidate Drug, Reduces Survivin Expression and Sensitizes A2780 Ovarian Cancer
Masahiro Yamamoto1, Shuhei Suzuki2,3, Keita Togashi2,4
1Department of Molecular Cancer Science, Yamagata University School of Medicine, Yamagata, Japan masahiro@med.id.yamagata-u.ac.jp m-okada@med.id.yamagata-u.ac.jp.
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 non-CSCs.
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.
Insights
AS602801, a c-Jun N-terminal kinase (JNK) inhibitor, enhances chemotherapy effectiveness in ovarian cancer stem cells (CSCs). It reduces survivin, an anti-apoptotic protein, making CSCs more sensitive to carboplatin and paclitaxel.
Area of Science:
- Oncology
- Cancer Stem Cell Biology
- Pharmacology
Background:
- Cancer stem cells (CSCs) possess tumor-initiation and metastatic potential.
- AS602801, a novel c-Jun N-terminal kinase (JNK) inhibitor, is known to suppress CSC properties.
- The chemosensitizing effect of AS602801 on CSCs remains unexplored.
Purpose of the Study:
- To investigate the potential of AS602801 to chemosensitize ovarian cancer stem cells (CSCs).
- To explore the underlying mechanisms of AS602801-mediated chemosensitization in combination with standard chemotherapeutics.
Main Methods:
- Utilized A2780 CSLC, an ovarian cancer-derived CSC line.
- Examined the combined effects of AS602801 with carboplatin and paclitaxel.
- Investigated the molecular mechanisms, including survivin expression.
Main Results:
- AS602801 significantly chemosensitized A2780 CSLC cells to carboplatin and paclitaxel.
- AS602801 treatment led to reduced expression of survivin, an anti-apoptotic protein.
- Survivin inhibition, both pharmacologically and genetically, also chemosensitized cells, and this effect was observed across various CSCs and non-CSCs.
Conclusions:
- AS602801 demonstrates chemosensitizing effects on ovarian CSCs by downregulating survivin.
- AS602801 is a promising therapeutic candidate targeting chemoresistance, tumor initiation, and metastasis in CSCs.
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