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曲格列酮诱导结肠癌细胞系分化及过氧化物酶体增殖物激活受体γ表达

Induction of differentiation and peroxisome proliferator-activated receptor gamma expression in colon cancer cell lines by troglitazone.

作者信息

Kato Masashi, Kusumi Tomomi, Tsuchida Shigeki, Tanaka Masanori, Sasaki Mutsuo, Kudo Hajime

机构信息

Second Department of Pathology, Hirosaki University School of Medicine, 5 Zaifu-cho, 036-8562, Japan.

出版信息

J Cancer Res Clin Oncol. 2004 Feb;130(2):73-9. doi: 10.1007/s00432-003-0510-2. Epub 2003 Nov 21.

Abstract

PURPOSE

We investigated the relationship between the effects of troglitazone (TGZ) on cellular growth, differentiation and apoptosis induction, and the induction of peroxisome proliferator-activated receptor (PPAR) gamma in three human colon cancer cell lines, HCT-15, DLD-1and LoVo.

METHODS

Viable cell number was evaluated by the Alamar blue assay and apoptotic cell death by TUNEL methods. Expression of PPARgamma mRNA and protein was examined by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot, respectively. The differentiation markers of colonic mucosa, villin and MUC2 mRNAs, were analyzed by real-time RT-PCR.

RESULTS

HCT-15 and DLD-1 cells proliferated rapidly while LoVo cells grew slowly. TGZ dose-dependently inhibited the proliferation of all the cell lines, and also induced apoptotic cell death. High expression of PPARgamma mRNA and protein was demonstrated in DLD-1 and LoVo cells before TGZ treatment. After the treatment, PPARgamma mRNA and protein levels were increased in HCT-15 and LoVo cells. Villin and MUC2 mRNAs were increased by TGZ treatment in HCT-15 cells while villin mRNA was repressed in LoVo cells. Changes in expression of PPARgamma, villin or MUC2 mRNAs were not observed in DLD-1 cells.

CONCLUSIONS

These results suggest that PPARgamma levels are not correlated with the rates of cell proliferation. Differentiation induction by TGZ was only observed in the cell lines with enhanced PPARgamma expression.

摘要

目的

我们研究了曲格列酮(TGZ)对三种人结肠癌细胞系HCT-15、DLD-1和LoVo细胞生长、分化及凋亡诱导的影响,以及过氧化物酶体增殖物激活受体(PPAR)γ的诱导情况之间的关系。

方法

通过alamar蓝分析法评估活细胞数量,用TUNEL法检测凋亡细胞死亡情况。分别通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测PPARγ mRNA和蛋白质的表达。通过实时RT-PCR分析结肠黏膜的分化标志物villin和MUC2 mRNA。

结果

HCT-15和DLD-1细胞增殖迅速,而LoVo细胞生长缓慢。TGZ剂量依赖性地抑制所有细胞系的增殖,并诱导凋亡细胞死亡。在TGZ处理前,DLD-1和LoVo细胞中PPARγ mRNA和蛋白质高表达。处理后,HCT-15和LoVo细胞中PPARγ mRNA和蛋白质水平升高。TGZ处理使HCT-15细胞中villin和MUC2 mRNA增加,而LoVo细胞中villin mRNA受到抑制。DLD-1细胞中未观察到PPARγ、villin或MUC2 mRNA表达的变化。

结论

这些结果表明PPARγ水平与细胞增殖速率无关。TGZ仅在PPARγ表达增强的细胞系中观察到分化诱导作用。

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