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蒌叶提取物增强5-氟尿嘧啶对HT29和HCT116结肠癌细胞生长的抑制作用中的细胞毒性效应。

Piper betle leaf extract enhances the cytotoxicity effect of 5-fluorouracil in inhibiting the growth of HT29 and HCT116 colon cancer cells.

作者信息

Ng Pek Leng, Rajab Nor Fadilah, Then Sue Mian, Mohd Yusof Yasmin Anum, Wan Ngah Wan Zurinah, Pin Kar Yong, Looi Mee Lee

机构信息

Department of Biomedical Sciences, Faculty of Allied Health, Universiti Kebangsaan Malaysia (UKM), Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia; UKM Medical Molecular Biology Institute (UMBI), Universiti Kebangsaan Malaysia (UKM), Jalan Yaacob Latiff, Bandar Tun Razak, Cheras, 56000 Kuala Lumpur, Malaysia; School of Biomedical Science, University of Nottingham Malaysia Campus, 43500 Semenyih, Selangor, Malaysia; Department of Biochemistry, Faculty of Medicine, Universiti Kebangsaan Malaysia (UKM), Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia; Forest Research Institute Malaysia (FRIM), 52109 Kuala Lumpur, Kepong, Malaysia; School of Biosciences, Taylor's University, Lakeside Campus, 47500 Subang Jaya, Selangor, Malaysia.

出版信息

J Zhejiang Univ Sci B. 2014 Aug;15(8):692-700. doi: 10.1631/jzus.B1300303.

Abstract

OBJECTIVE

The combination effect of Piper betle (PB) and 5-fluorouracil (5-FU) in enhancing the cytotoxic potential of 5-FU in inhibiting the growth of colon cancer cells was investigated.

METHODS

HT29 and HCT116 cells were subjected to 5-FU or PB treatment. 5-FU and PB were then combined and their effects on both cell lines were observed after 24 h of treatment. PB-5-FU interaction was elucidated by isobologram analysis. Apoptosis features of the treated cells were revealed by annexin V/PI stain. High-performance liquid chromatography (HPLC) was performed to exclude any possible chemical interaction between the compounds.

RESULTS

In the presence of PB extract, the cytotoxicity of 5-FU was observed at a lower dose (IC50 12.5 µmol/L) and a shorter time (24 h) in both cell lines. Both cell lines treated with 5-FU or PB alone induced a greater apoptosis effect compared with the combination treatment. Isobologram analysis indicated that PB and 5-FU interacted synergistically and antagonistically in inhibiting the growth of HT29 and HCT116 cells, respectively.

CONCLUSIONS

In the presence of PB, a lower dosage of 5-FU is required to achieve the maximum drug effect in inhibiting the growth of HT29 cells. However, PB did not significantly reduce 5-FU dosage in HCT116 cells. Our result showed that this interaction may not solely contribute to the apoptosis pathway.

摘要

目的

研究蒌叶(PB)与5-氟尿嘧啶(5-FU)联合应用增强5-FU抑制结肠癌细胞生长的细胞毒性作用。

方法

对HT29和HCT116细胞进行5-FU或PB处理。然后将5-FU和PB联合应用,处理24小时后观察它们对两种细胞系的影响。通过等高线图分析阐明PB-5-FU的相互作用。用膜联蛋白V/碘化丙啶染色揭示处理后细胞的凋亡特征。采用高效液相色谱法(HPLC)排除化合物之间任何可能的化学相互作用。

结果

在存在PB提取物的情况下,在两种细胞系中均观察到较低剂量(IC50为12.5 μmol/L)和较短时间(24小时)的5-FU细胞毒性。与联合处理相比,单独用5-FU或PB处理的两种细胞系均诱导出更大的凋亡效应。等高线图分析表明,PB和5-FU分别在抑制HT29和HCT116细胞生长中表现出协同和拮抗作用。

结论

在存在PB的情况下,抑制HT29细胞生长达到最大药物效应所需的5-FU剂量较低。然而,PB并未显著降低HCT116细胞中的5-FU剂量。我们的结果表明,这种相互作用可能不仅仅作用于凋亡途径。

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