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Updated: May 11, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Effectiveness of tumor‑treating fields to reduce the proliferation and migration of liposarcoma cell lines
Won Seok Lee1, Yoonjung Jang2, Ahyeon Cho3
1Department of Biochemistry, School of Medicine, Daegu Catholic University, Daegu, Gyeongsangbuk-do 42472, Republic of Korea.
Abstract:
Liposarcoma (LPS) is a rare type of soft tissue sarcoma that constitutes 20% of all sarcoma cases in adults. Effective therapeutic protocols for human LPS are not well-defined. Tumor-treating fields (TTFields) are a novel and upcoming field for antitumor therapy. TTFields combined with chemoradiotherapy have proven to be more effective than TTFields combined with radiotherapy or chemotherapy alone. The present study aimed to assess the effectiveness of TTFields in inhibiting cell proliferation and viability for the anticancer treatment of LPS. The present study used TTFields (frequency, 150 kHz; intensity, 1.0 V/cm) to treat two LPS cell lines (94T778 and SW872) and analyzed the antitumor effects. According to trypan blue and MTT assay results, TTFields markedly reduced the viability and proliferation of LPS cell lines along with the formation of colonies in three-dimensional culture. Based on the Transwell chamber assay, TTFields treatment also markedly reduced the migration of LPS cells. Furthermore, as shown by the higher activation of caspase-3 in the Caspase-3 activity assay and the results of the reactive oxygen species (ROS) assay, TTFields increased the formation of ROS in the cells and enhanced the proportion of apoptotic cells. The present study also investigated the inhibitory effect of TTFields in combination with doxorubicin (DOX) on the migratory capacity of tumor cells. The results demonstrated that TTFields treatment synergistically induced the ROS-induced apoptosis of LPS cancer cell lines and inhibited their migratory behavior. In conclusion, the present study demonstrated the potential of TTFields in improving the sensitivity of LPS cancer cells, which may lay the foundation for future clinical trials of this combination treatment strategy.
Insights
Tumor-treating fields (TTFields) show promise in treating liposarcoma (LPS) by inhibiting cancer cell proliferation, viability, and migration. This novel therapy, especially combined with doxorubicin, induces apoptosis and may form the basis for future clinical trials.
Area of Science:
- Oncology
- Biophysics
- Cancer Therapeutics
Background:
- Liposarcoma (LPS) is a rare soft tissue sarcoma with poorly defined therapeutic strategies.
- Tumor-treating fields (TTFields) represent a novel approach in antitumor therapy.
- Previous research suggests TTFields combined with chemoradiotherapy enhance efficacy.
Purpose of the Study:
- To evaluate the efficacy of TTFields in inhibiting liposarcoma cell proliferation and viability.
- To investigate the impact of TTFields on LPS cell migration and apoptosis.
- To explore the synergistic effects of TTFields combined with doxorubicin (DOX) on LPS cells.
Main Methods:
- Treatment of two LPS cell lines (94T778 and SW872) with TTFields (150 kHz, 1.0 V/cm).
- Assays used include trypan blue, MTT, Transwell chamber, Caspase-3 activity, and reactive oxygen species (ROS) assays.
- Evaluation of combined TTFields and DOX treatment on cell migration.
Main Results:
- TTFields significantly reduced LPS cell viability, proliferation, and colony formation in 3D culture.
- TTFields treatment markedly decreased LPS cell migration and increased apoptosis via ROS generation and caspase-3 activation.
- Combination therapy with TTFields and DOX synergistically enhanced ROS-induced apoptosis and inhibited migration.
Conclusions:
- TTFields demonstrate significant potential in inhibiting liposarcoma cell growth, migration, and inducing apoptosis.
- The combination of TTFields and doxorubicin shows synergistic effects, enhancing anti-cancer activity.
- These findings provide a foundation for investigating TTFields as a therapeutic strategy for liposarcoma in clinical settings.
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