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Krüppel-like factor 4 promotes high-mobility group box 1-induced chemotherapy resistance in osteosarcoma cells
Jun Huang1, Ke Liu2, Deye Song1
1Department of Orthopaedics, The 2nd Xiangya Hospital, Central South University, Changsha, China.
Abstract:
Osteosarcoma is the most common primary malignant bone tumor, and the frequent acquisition of chemoresistance is often an obstacle to achieving favorable outcomes during chemotherapy. Recently, Krüppel-like factor 4 (KLF4) has been shown to be associated with chemotherapy resistance in a few tumors; however, the involvement of KLF4 in chemotherapy resistance in osteosarcoma cells remains unknown. In this study, quantitative real-time PCR and western blot analysis revealed that KLF4 expression was significantly increased in response to cisplatin, methotrexate and doxorubicin treatment in osteosarcoma cells, and knockdown of KLF4 increased sensitivity to these anticancer drugs by decreasing cellular clonogenic ability and increasing apoptosis. Moreover, our data suggest that KLF4-regulated drug resistance might, at least partially, positively regulate high-mobility group box 1 (HMGB1), which was found to be a significant contributor to chemoresistance in osteosarcoma cells in our previous study. In summary, this study highlights the significance of KLF4/HMGB1 interaction in regulating chemotherapy resistance, and suggests that targeting KLF4/high-mobility group box 1 may be a therapeutic strategy for osteosarcoma chemotherapy.
Insights
Krüppel-like factor 4 (KLF4) promotes chemotherapy resistance in osteosarcoma. Targeting the KLF4/high-mobility group box 1 (HMGB1) interaction may improve osteosarcoma treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Osteosarcoma is the most common primary bone cancer.
- Chemoresistance is a major challenge in treating osteosarcoma.
- Krüppel-like factor 4 (KLF4) is implicated in chemotherapy resistance in other cancers.
Purpose of the Study:
- To investigate the role of KLF4 in chemotherapy resistance in osteosarcoma cells.
- To explore the relationship between KLF4 and high-mobility group box 1 (HMGB1) in osteosarcoma chemoresistance.
Main Methods:
- Quantitative real-time PCR and western blot analysis to measure KLF4 expression.
- KLF4 knockdown experiments to assess drug sensitivity.
- Evaluation of cellular clonogenic ability and apoptosis.
Main Results:
- KLF4 expression increased in osteosarcoma cells treated with cisplatin, methotrexate, and doxorubicin.
- KLF4 knockdown enhanced sensitivity to these chemotherapy drugs.
- KLF4 positively regulates HMGB1, a known contributor to osteosarcoma chemoresistance.
Conclusions:
- KLF4 plays a significant role in regulating chemotherapy resistance in osteosarcoma.
- The KLF4/HMGB1 interaction is crucial for chemoresistance in osteosarcoma.
- Targeting KLF4 and HMGB1 presents a potential therapeutic strategy for osteosarcoma.
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