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应用基因芯片分析高转移和低转移人卵巢癌细胞系的基因表达谱差异

Gene expression profile differences in high and low metastatic human ovarian cancer cell lines by gene chip.

作者信息

Xu Shenhua, Mou Hanzhou, Lü Guiquan, Zhu Chihong, Yang Zhengyan, Gao Yongliang, Lou Hongkun, Liu Xianglin, Cheng Yong, Yang Wen

机构信息

Zhejiang Cancer Research Institute, Hangzhou 310022, China.

出版信息

Chin Med J (Engl). 2002 Jan;115(1):36-41.

PMID:11930655
Abstract

OBJECTIVES

To study the difference between gene expressions of high (H0-8910PM) and low (HO-8910) metastatic human ovarian carcinoma cell lines and screen novel associated genes by cDNA microarray.

METHODS

cDNA retro-transcribed from equal quantities of mRNA derived from high and low metastatic tumor cells or normal ovarian tissues were labeled with Cy5 and Cy3 fluorescein as probes. The mixed probe was hybridized with two pieces of BioDoor 4096 double dot human whole gene chip and scanned with a ScanArray 3000 laser scanner. The acquired image was analyzed by ImaGene 3.0 software.

RESULTS

A total of 355 genes with expression levels more than 3 times larger were found by comparing the HO-8910 cell with normal ovarian epithelial cells. A total of 323 genes with expression levels more than 3 times larger in HO-8910PM cells compared to normal ovarian epithelium cells were also detected. A total of 165 genes whose expression levels were more than two times those of HO-8910PM cells compared to their mother cell line (HO-8910) were detected. Twenty-one genes with expression levels > 3 times were found from comparison of these two tumor cell lines.

CONCLUSIONS

cDNA microarray techniques are effective in screening differential gene expression between two human ovarian cancer cell lines (H0-8910PM; HO-8910) and normal ovarian epithelial cells. These genes may be related to the genesis and development of ovarian carcinoma. Analysis of the human ovarian cancer gene expression profile with cDNA microarray may help in gene diagnosis, treatment and prevention.

摘要

目的

研究高转移(H0 - 8910PM)和低转移(HO - 8910)人卵巢癌细胞系基因表达的差异,并通过cDNA微阵列筛选新的相关基因。

方法

从高转移和低转移肿瘤细胞或正常卵巢组织等量mRNA逆转录得到的cDNA,分别用Cy5和Cy3荧光素标记作为探针。混合探针与两张BioDoor 4096双点人全基因芯片杂交,并用ScanArray 3000激光扫描仪扫描。采集的图像用ImaGene 3.0软件分析。

结果

与正常卵巢上皮细胞相比,HO - 8910细胞中发现共有355个基因表达水平增加超过3倍。与正常卵巢上皮细胞相比,HO - 8910PM细胞中也检测到共有323个基因表达水平增加超过3倍。与母细胞系(HO - 8910)相比,检测到共有165个基因表达水平是HO - 8910PM细胞的两倍以上。比较这两种肿瘤细胞系发现21个基因表达水平> 3倍。

结论

cDNA微阵列技术可有效筛选两个人卵巢癌细胞系(H0 - 8910PM;HO - 8910)与正常卵巢上皮细胞之间的差异基因表达。这些基因可能与卵巢癌的发生发展有关。用cDNA微阵列分析人卵巢癌基因表达谱可能有助于基因诊断、治疗和预防。

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