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Updated: Jan 21, 2026

Enrichment for Chemoresistant Ovarian Cancer Stem Cells from Human Cell Lines
Published on: September 10, 2014
CHTOP in Chemoresistant Epithelial Ovarian Cancer: A Novel and Potential Therapeutic Target
Xiaojie Feng1,2,3, Xupeng Bai2,3, Jie Ni2,3
1Department of Gynaecological Oncology, Henan Cancer Hospital, Zhengzhou, China.
Abstract:
Objective: Chemoresistance is a major challenge in epithelial ovarian cancer (EOC) treatment. Chromatin target of protein arginine methyltransferase (CHTOP) was identified as a potential biomarker in chemoresistant EOC cell lines using label-free LC-MS/MS quantitative proteomics. Thus, the aim of this study is to investigate the role of CHTOP in chemoresistant EOC and the underlying mechanism. Methods: The expression of CHTOP in human ovarian cancer cells and tissues was detected using immunofluorescence (IF), western blot (WB), and immunohistochemistry (IHC), respectively. Flow cytometry and TUNEL assay were employed to detect the effect of CHTOP knockdown (KD) in chemoresistant EOC cell apoptosis, while colony and sphere formation assays were used to evaluate its effect on cell stemness. The association of CHTOP with cell metastasis was determined using Matrigel invasion and wound-healing assays. Results: The higher level expression of CHTOP protein was found in chemoresistant EOC cells as compared to their sensitive parental cells or normal epithelial ovarian cells. Results from IHC and bioinformatic analysis showed CHTOP was highly expressed in human ovarian cancer tissues and associated with a poor progression-free survival in patients. In addition, CHTOP KD significantly enhanced cisplatin-induced apoptosis, reduced the stemness of chemoresistant EOC cells, and decreased their metastatic potential. Conclusion: Our findings suggest that CHTOP is associated with apoptosis, stemness, and metastasis in chemoresistant EOC cells and might be a promising target to overcome chemoresistance in EOC treatment.
Insights
Chromatin target of protein arginine methyltransferase (CHTOP) is highly expressed in chemoresistant epithelial ovarian cancer (EOC). Reducing CHTOP enhances apoptosis and decreases stemness and metastasis, suggesting it as a therapeutic target for EOC.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Chemoresistance presents a significant hurdle in treating epithelial ovarian cancer (EOC).
- Chromatin target of protein arginine methyltransferase (CHTOP) was identified as a potential biomarker in chemoresistant EOC cell lines.
- Understanding CHTOP's role is crucial for developing novel therapeutic strategies against EOC.
Purpose of the Study:
- To investigate the role of CHTOP in chemoresistant EOC.
- To elucidate the underlying mechanisms by which CHTOP influences chemoresistance.
- To evaluate CHTOP as a potential therapeutic target for overcoming EOC chemoresistance.
Main Methods:
- Detected CHTOP expression in ovarian cancer cells and tissues using immunofluorescence, western blot, and immunohistochemistry.
- Assessed apoptosis, stemness, and metastasis in chemoresistant EOC cells following CHTOP knockdown (KD) using flow cytometry, TUNEL assay, colony/sphere formation assays, and invasion/wound-healing assays.
- Utilized bioinformatic analysis to correlate CHTOP expression with patient survival.
Main Results:
- CHTOP was significantly upregulated in chemoresistant EOC cells and human ovarian cancer tissues, correlating with poor progression-free survival.
- CHTOP knockdown enhanced cisplatin-induced apoptosis in chemoresistant EOC cells.
- CHTOP KD reduced cancer stemness and decreased the metastatic potential of chemoresistant EOC cells.
Conclusions:
- CHTOP plays a critical role in promoting apoptosis resistance, stemness, and metastasis in chemoresistant EOC.
- Targeting CHTOP presents a promising strategy to overcome chemoresistance in epithelial ovarian cancer.
- CHTOP is a potential biomarker and therapeutic target for improving EOC treatment outcomes.
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