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Updated: Apr 22, 2026

Radiosensitivity of Cancer Stem Cells in Lung Cancer Cell Lines
Published on: August 21, 2019
Survivin silencing enhances radiosensitivity in oral squamous cell carcinoma cell
1Department of Stomatology, the Affiliated Hospital of Qingdao University, Qingdao, Shandong, China. sunhuibinqd@126.com.
Objective:
Survivin is a member of the inhibitor of apoptosis protein (IAP) family. It is overexpressed in most cancer tissues and induces resistance to radiation therapy. In this study, we investigated whether knockdown of survivin by siRNA could induce apoptosis and enhance radiosensitivity in oral squamous cell carcinoma cells (OSCC).
Materials And Methods:
Oral squamous cell carcinoma cell lines KB was subjected to radiotherapy, small interfering RNA (siRNA) targeting survivin was transfected into KB cells in vitro, then subjected to radiotherapy. After irradiation or/and siRNA transfection, viable and dead cells were counted to determine radiation sensitivity by MTT assay, proliferation by colony-forming ability and apoptosis was analyzed by flow cytometry. Tumor-bearing mice were irradiated with 6 Gy of 60 Co-γ radiator.
Results:
The results showed knockdown of survivin in KB cells showed reduced cell proliferation and increased number of radiation-induced apoptosis. Apoptosis was increased by survivin silencing alone and increased further in combination with irradiation. Colony formation was significantly reduced by survivin silencing in combination with irradiation.
Conclusions:
Survivin silencing sensitizes KB cells toward irradiation. Survivin silencing in combination with radiation inhibits cell proliferation and colony formation significantly and increases apoptosis more than each single treatment alone. In addition, survivin silencing significantly enhanced inhibition of tumor growth and potentiated cell apoptosis by irradiation in KB xenografts. In conclusion, survivin silencing could enhance sensitivity of human KB cells to radiotherapy in vitro and in vivo.
Insights
Survivin silencing enhances radiosensitivity in oral squamous cell carcinoma (OSCC) cells. Combining survivin knockdown with radiation therapy significantly boosts apoptosis and inhibits tumor growth in vitro and in vivo.
Area of Science:
- Oncology
- Molecular Biology
- Radiotherapy Research
Background:
- Survivin, an inhibitor of apoptosis protein, is overexpressed in cancers and confers resistance to radiation therapy.
- Oral squamous cell carcinoma (OSCC) exhibits survivin overexpression, contributing to treatment resistance.
Purpose of the Study:
- To investigate the effect of survivin knockdown using siRNA on apoptosis induction and radiosensitivity in OSCC cells.
- To evaluate the combined efficacy of survivin silencing and radiotherapy in vitro and in vivo.
Main Methods:
- Oral squamous cell carcinoma (OSCC) KB cell lines were treated with radiotherapy and/or survivin-targeting siRNA.
- Cell viability, proliferation (colony-forming ability), and apoptosis were assessed using MTT assay and flow cytometry.
- Tumor-bearing mice models were used to evaluate in vivo efficacy.
Main Results:
- Survivin knockdown reduced cell proliferation and increased radiation-induced apoptosis in KB cells.
- Apoptosis was augmented by survivin silencing, especially when combined with irradiation.
- Colony formation was significantly inhibited by the combination of survivin silencing and irradiation.
Conclusions:
- Survivin silencing sensitizes OSCC cells to radiotherapy, enhancing apoptosis and inhibiting proliferation and colony formation.
- The combination of survivin silencing and radiation therapy demonstrates significant therapeutic potential in both in vitro and in vivo models of OSCC.
- Survivin silencing potentiates the anti-tumor effects of irradiation, offering a promising strategy for improving OSCC treatment outcomes.
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