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[5-氮杂-2'-脱氧胞苷诱导人结肠癌细胞中CDH13表达的抑制及其对体外甲基化状态和裸鼠异种移植瘤生长的抑制作用]

[5-aza-2'-deoxycytidine-induced inhibition of CDH13 expression and its inhibitory effect on methylation status in human colon cancer cells in vitro and on growth of xenograft in nude mice].

作者信息

Ren Jian-zhen, Huo Ji-rong

机构信息

Department of Gastroenterology,Central Southern University, Changsha, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2012 Jan;34(1):6-10.

Abstract

OBJECTIVE

To determine the inhibitory effect of 5-aza-2'-deoxycytidine (5-Aza-CdR) on the growth of human colon carcinoma cells and xenografts in nude mice, to observe its effect on CDH13 gene expression and methylation in the xenografts, and to explore the possible mechanisms.

METHODS

Human colon carcinoma cell line HCT116 cells were treated with 5-Aza-CdR, and the cell morphology was observe by phase contrast microscopy. The cell growth was assessed by MTT assay. A tumor-bearing mouse model was generated by subcutaneous inoculation of human colon carcinoma HCT116 cells into nude mice. The tumor growth in the nude mice was observed, the CDH13 gene expression and its methylation status in the tumors were detected using methylation specific PCR (MSP), RT-PCR, Western blotting and immunohistochemistry.

RESULTS

After treatment with 5-Aza-CdR, the inhibition rate of the growth of cultured HCT116 cells was increased as the concentration was increasing. The growth of the xenografts in nude mice was significantly inhibited, and the methylated CDH13 gene was reactivated. After 4 weeks of 5-Aza-CdR treatment, no significant difference was found between the body weights of nude mice in the 5-Aza-CdR group [(18.06 ± 1.29) g] and control group [(17.07 ± 0.84) g], (P > 0.10), and the average volume of xenografts of the 5-Aza-CdR group was (907.00 ± 87.29) mm(3), significantly smaller than the (1370.93 ± 130.20) mm(3) in the control group (P < 0.005). No expression of CDH13 gene was found in the control group. The expression of CDH13 gene in the 5-Aza-CdR group was increased along with the increasing concentration of 5-Aza-CdR.

CONCLUSIONS

5-Aza-CdR inhibits the growth of human colon cancer cells in culture and in nude mice, and induces the cancer cells to re-express CDH13 in nude mice. Its mechanism may be that demethylation of the methylated CDH13 promoter induced by 5-Aza-CdR restores CDH13 expression and thus inhibits the tumor growth in nude mice.

摘要

目的

探讨5-氮杂-2'-脱氧胞苷(5-Aza-CdR)对人结肠癌细胞及裸鼠移植瘤生长的抑制作用,观察其对移植瘤中CDH13基因表达及甲基化的影响,并探讨其可能机制。

方法

用5-Aza-CdR处理人结肠癌细胞系HCT116细胞,相差显微镜观察细胞形态变化,MTT法检测细胞生长情况。将人结肠癌HCT116细胞皮下接种于裸鼠建立荷瘤小鼠模型,观察裸鼠肿瘤生长情况,采用甲基化特异性PCR(MSP)、RT-PCR、Western印迹及免疫组化检测肿瘤组织中CDH13基因表达及甲基化状态。

结果

5-Aza-CdR处理后,培养的HCT116细胞生长抑制率随药物浓度增加而升高。裸鼠移植瘤生长明显受抑制,甲基化的CDH13基因被重新激活。5-Aza-CdR处理4周后,5-Aza-CdR组裸鼠体重[(18.06±1.29)g]与对照组[(17.07±0.84)g]相比,差异无统计学意义(P>0.10);5-Aza-CdR组移植瘤平均体积为(907.00±87.29)mm³,明显小于对照组的(1370.93±130.20)mm³(P<0.005)。对照组未检测到CDH13基因表达,5-Aza-CdR组CDH13基因表达随药物浓度增加而升高。

结论

5-Aza-CdR可抑制体外培养的人结肠癌细胞及裸鼠移植瘤生长,并诱导裸鼠移植瘤中癌细胞重新表达CDH13。其机制可能是5-Aza-CdR诱导甲基化的CDH13启动子去甲基化,恢复CDH13表达,从而抑制裸鼠肿瘤生长。

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