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Updated: Feb 13, 2026

Radiosensitivity of Cancer Stem Cells in Lung Cancer Cell Lines
Published on: August 21, 2019
Slug inhibition increases radiosensitivity of nasopharyngeal carcinoma cell line C666-1
Hongxia Yang1, Gang Zhang2, Xiaolin Che3
1Department of Otorhinolaryngology, Maternal and Child Health Hospital of Tai'an, Tai'an, Shandong 271000, P.R. China.
Abstract:
Slug is associated with the radioresistance of nasopharyngeal carcinoma (NPC) and the main current approach of treatment for NPC is radiotherapy. Hence, the aim of the current study was to determine the effect of Slug silencing on the radiosensitivity of NPC cells. Lentiviral-mediated transfection of Slug RNA interference (RNAi) in NPC cell line C666-1 was performed in vitro. Following Slug inhibition, its expression was detected using western blotting. A clonogenic survival assay and flow cytometry were then performed to evaluate the clonogenic cell survival, cell cycle distribution and apoptosis of C666-1 cells following irradiation. The results indicated that Slug RNAi decreased cell proliferation, and increased cell apoptosis and G0/G1 arrest. Thus, lentiviral-mediated transfection of Slug RNAi enhanced the radiosensitivity of the NPC cell line C666-1, and Slug may therefore be a potential target to improve radiotherapy in treatment of NPC and reduce the radioresistance of NPC.
Insights
Silencing Slug in nasopharyngeal carcinoma (NPC) cells using RNA interference enhanced their sensitivity to radiotherapy. This suggests Slug is a potential therapeutic target to improve NPC treatment outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Radiotherapy Research
Background:
- Nasopharyngeal carcinoma (NPC) is often treated with radiotherapy.
- Tumor radioresistance is a significant challenge in NPC treatment.
- The transcription factor Slug is implicated in cancer radioresistance.
Purpose of the Study:
- To investigate the effect of Slug silencing on the radiosensitivity of NPC cells.
- To determine if targeting Slug can overcome radioresistance in NPC.
Main Methods:
- NPC cell line C666-1 was transfected with lentiviral Slug RNA interference (RNAi) in vitro.
- Slug expression was confirmed via western blotting.
- Clonogenic survival assays and flow cytometry assessed radiosensitivity, cell cycle, and apoptosis post-irradiation.
Main Results:
- Slug RNAi significantly reduced NPC cell proliferation.
- Inhibition of Slug increased apoptosis and induced G0/G1 cell cycle arrest.
- Radiosensitivity of C666-1 cells was markedly enhanced following Slug silencing.
Conclusions:
- Lentiviral-mediated Slug RNAi improves the radiosensitivity of NPC cells.
- Slug represents a promising therapeutic target for enhancing radiotherapy efficacy in NPC.
- Targeting Slug may help reduce radioresistance in nasopharyngeal carcinoma treatment.
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