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Phenethyl isothiocyanate enhances adriamycin‑induced apoptosis in osteosarcoma cells
Qie Fan1, Xinli Zhan1, Zengming Xiao1
1Department of Spinal Surgery, The First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, P.R. China.
Abstract:
Adriamycin (ADM) is a first‑line agent administered during the therapeutic regimes against osteosarcoma. Clinical administration of ADM produces systemic toxicity and resistance in patients, which restricts its applicability. In the present study the effects of phenethyl isothiocyanate (PEITC) on ADM‑induced apoptosis in osteosarcoma cells was evaluated. Using U2‑OS osteosarcoma cell line cells, treatment with PEITC or ADM for 24 h was observed to dose‑dependently inhibit proliferation of U2‑OS cells with half maximal inhibitory concentration (IC50) values of 5.33 µM and 10.32 µg/ml, respectively. When U2‑OS cells were treated with a combination of the two agents, the inhibition was apparently enhanced, as the IC50 values decreased to 2 µM for PEITC and 1 µg/ml for ADM. Flow cytometry and terminal deoxynucleotidyl transferase dUTP nick end labeling revealed that treatment with PEITC or ADM alone reduced the viability of the U2‑OS cells. Furthermore, the viability of the U2‑OS cells was additionally reduced when treatment was with PEITC and ADM together. Supporting this finding, the activity and expression of caspase‑3 were observed to be enhanced in the U2‑OS cells following treatment with either PEITC or ADM, or a combination of the two. These results clearly indicate that PEITC enhances ADM‑induced apoptosis in osteosarcoma cells.
Insights
Phenethyl isothiocyanate (PEITC) enhances Adriamycin (ADM) effectiveness against osteosarcoma. This combination therapy boosts ADM-induced apoptosis in cancer cells, offering a potential strategy to overcome treatment resistance.
Area of Science:
- Oncology
- Pharmacology
- Cell Biology
Background:
- Adriamycin (ADM) is a key chemotherapy for osteosarcoma but faces limitations due to toxicity and resistance.
- Developing strategies to enhance ADM efficacy and overcome resistance is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the synergistic effects of phenethyl isothiocyanate (PEITC) on ADM-induced apoptosis in osteosarcoma cells.
- To evaluate PEITC as a potential sensitizer to ADM therapy.
Main Methods:
- Utilized the U2-OS osteosarcoma cell line.
- Assessed cell proliferation inhibition using IC50 values.
- Quantified apoptosis via flow cytometry and TUNEL assay.
- Measured caspase-3 activity and expression levels.
Main Results:
- Both PEITC and ADM dose-dependently inhibited U2-OS cell proliferation.
- Combined treatment significantly enhanced growth inhibition (lower IC50 values for both agents).
- PEITC and ADM individually reduced cell viability, with a greater reduction when used together.
- Caspase-3 activity and expression were notably increased by combination therapy.
Conclusions:
- Phenethyl isothiocyanate (PEITC) significantly potentiates ADM-induced apoptosis in osteosarcoma cells.
- The combination of PEITC and ADM demonstrates enhanced anti-cancer effects.
- PEITC shows promise as an adjuvant therapy to improve osteosarcoma treatment outcomes.
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