Abstract

Tongue squamous cell carcinoma is the most common malignant tumor in oral and maxillofacial regions. Recent research has found that artemether can inhibit growth and induce apoptosis of cancer cells, although the mechanism is not clear. The present study aimed to explore the correlation between the HSP90/Akt pathway and artemether‐induced apoptosis of Cal27 cells. A cell counting kit‐8 and flow cytometry were used to detect the proliferation and apoptosis of Cal27 cells, respectively, mRNA expression was examined by quantitative RT‐PCR, and protein expression was detected by western blotting. Our data revealed that artemether can inhibit growth and induce apoptosis of Cal27 cells. As the artemether concentration was increased, we observed downregulation of the expression of HSP90, p‐Akt and p‐mTOR in Cal27 cells, whereas the expression of Akt was not significantly changed. We also observed a time‐dependent decrease in the expression of HSP90, p‐Akt and p‐mTOR during exposure to 0.1 mg·mL−1 artemether. In conclusion, the HSP90/Akt pathway may be involved in artemether‐induced apoptosis of Cal27 cells.

Highlights

  • Tongue squamous cell carcinoma is the most common malignant tumor in oral and maxillofacial regions

  • The present study aimed to explore the correlation between the HSP90/Akt pathway and artemether-induced apoptosis of Cal27 cells

  • We found that the HSP90/Akt pathway may be involved in artemether inhibiting Cal27 cell growth and inducing apoptosis

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Summary

Introduction

Tongue squamous cell carcinoma is the most common malignant tumor in oral and maxillofacial regions. The present study aimed to explore the correlation between the HSP90/Akt pathway and artemether-induced apoptosis of Cal cells. The HSP90/Akt pathway may be involved in artemether-induced apoptosis of Cal cells. Tongue squamous cell carcinoma (TSCC) is the most common malignant tumor in oral and maxillofacial area, characterized by high degree of malignancy, a high proliferation rate, strong invasiveness and easy occurrence of neck lymphatic metastasis [1–3]. Abbreviations ANOVA, analysis of variance; CCK-8, cell counting kit-8; DMEM, Dulbecco’s modified Eagle’s medium; FITC, fluorescein isothiocyanate; HSP, heat shock protein, mTOR, mammalian target of rapamycin, PBS, phosphate-buffered saline, PI, propidium iodide; TSCC, tongue squamous cell carcinoma; TUNEL, terminal deoxynucleotidyl transferase dUTP nick end labeling.

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