Upregulated expression of S100A6 in human gastric cancer

被引:36
|
作者
Yang, Yan Qing [1 ,2 ]
Zhang, Lan Jing [2 ]
Dong, Hui [3 ]
Jiang, Chang Long [2 ]
Zhu, Zheng Gang [4 ]
Wu, Jian Xin [5 ]
Wu, Yun Lin [6 ]
Han, Jun Song [2 ]
Xiao, Hua Sheng [2 ]
Gao, Heng Jun [2 ]
Zhang, Qing Hua [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Ruijin Hosp, Shanghai Inst Hematol, State Key Lab Med Gen, Shanghai 200025, Peoples R China
[2] Natl Engn Ctr Biochip Shanghai, Shanghai, Peoples R China
[3] Chinese Natl Human Genome Ctr, Shanghai, Peoples R China
[4] Shanghai Jiao Tong Univ, Ruijin Hosp, Dept Surg, Sch Med, Shanghai 200025, Peoples R China
[5] Shanghai Jiao Tong Univ, Xinhua Hosp, Dept Gastroenterol, Sch Med, Shanghai 200025, Peoples R China
[6] Shanghai Jiao Tong Univ, Sch Med, Dept Gastroenterol, Ruijin Hosp, Shanghai 200025, Peoples R China
关键词
microarray; neoplasma of the stomach; S100A6; serial analysis of gene expression; tissue microarray;
D O I
10.1111/j.1751-2980.2007.00311.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
OBJECTIVE: The expression of S100A6 (calcyclin), a member of the S100 calcium binding protein family, is elevated in a number of malignant tumors, but there have been few reports about its expression in gastric cancer. The aim of this study was to investigate its expression regulations in human gastric cancer and noncancerous mucosa, and the response to chemotherapeutic drugs in the gastric cancer cell line. MATERIALS AND METHODS: In one matched gastric cancer sample pair, the serial analysis of gene expression (SAGE) experiment was conducted to compare the gene expression profiles between cancerous and adjacent tissues. To detect the expression regulations among more cancerous tissues, microarrays were carried out and real-time RT-PCR was conducted to validate the results. At the protein level, Western blot and tissue microarray (TMA) examination were further used to verify S100A6 expression. The regulation. detection of S100A6 with flurouracil and doxorubicin at the mRNA and protein level was performed in the SGC7901 cell line. RESULTS: With the SAGE strategy, five times more S100A6 tags were identified in cancer tissues than in normal tissues. With the cDNA microarray, S100A6 was found to be significantly upregulated in 21 of 42 (50%) nonselective gastric cancers. In 10 other paired samples, the upregulation of S 100A6 was consolidated with RT-PCR and Western blot analysis as well. A total of 14 endoscopy-sectioned gastric noncancerous lesions and corresponding normal gastric mucosa were also applied to profile the gene expression; both cDNA microarray and RT-PCR demonstrated no significant alterations of S 100A6 at the mRNA level. TMA examination showed that 34 of 52 (65.4%) cancer samples were positively stained, while only 17 of 80 (21.3%) noncancerous lesions were positively detected and all nine normal mucosae were detected to be negative. An in vitro experiment showed that in the gastric cell line SGC-7901, S100A6 mRNA was detected to be upregulated from 24 to 72 h after treatment with 5 mg/L 5-flurouracil or 0.3 mg/L doxorubicin, and there were two wave upregulations of the S100A6 protein. CONCLUSION: The observed regulated expression of S100A6 suggests that it is associated with gastric cancer tumorigenesis and quantitation of S100A6 is a promising tool for diagnosis of gastric cancer.
引用
收藏
页码:186 / 193
页数:8
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