Abstract

We used the fluorescence ubiquitination-based cell cycle indicator (FUCCI) to monitor cell cycle arrest after treatment of FUCCI-expressing HeLa cells (FUCCI-HeLa) with a traditional Chinese medicine (TCM) herbal mixture LQ, previously shown to have anti-tumor and anti-metastatic activity in mouse models. Paclitaxel was used as the positive control. In 2D monolayer culture, the untreated control had approximately 45% of the cells in S/G₂/M phase. In contrast, the LQ-treated cells (9 mg/ml) were mostly in the G₀/G₁ (>90%) after 72 hours. After treatment with paclitaxel (0.01 μm), for 72 hours, 95% of the cells were in S/G₂/M. In 2.5D Matrigel culture, the colonies in the untreated control group had 40% of the cells in S/G₂/M. LQ arrested the cells in G₀/G₁ after 72 hours. Paclitaxel arrested almost all the cells in S/G₂/M after 72 hours. In 3D Gelfoam culture, the untreated control culture had approximately 45% of cells in G₂/M. In contrast, the LQ-treated cells were mostly in G₀/G₁ phase (>80%) after 72 hours treatment. Paclitaxel resulted in 90% of the cells arrested in S/G₂/M after 72 hours. The present report suggests the non-toxic LQ has potential to maintain cancers in a quiescent state for long periods of time.

Highlights

  • Traditional Chinese medicine (TCM) composi­ tions usually comprise multiple herbs and many components may be are necessary for efficacy

  • Effect of LQ or paclitaxel on the cell-cycle phase distribution of fluorescence ubiquitination-based cell cycle indicator (FUCCI)-HeLa cells growing in 2D culture

  • After treatment with LQ (9 mg/ml) for 72 hours, the HeLa-FUCCI cells were almost all arrested in G0/G1

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Summary

Introduction

Traditional Chinese medicine (TCM) composi­ tions usually comprise multiple herbs and many components may be are necessary for efficacy. In 2D monolayer culture, the untreated control had approximately 45% of the cells in S/G2/M phase. Paclitaxel resulted in 90% of the cells arrested in S/G2/M after 72 hours. The present report uses FUCCI imaging to demon­ strate the effect of LQ on the cell cycle arrest of HeLa cells.

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