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S100A6在人胃癌中的表达上调。

Upregulated expression of S100A6 in human gastric cancer.

作者信息

Yang Yan Qing, Zhang Lan Jing, Dong Hui, Jiang Chang Long, Zhu Zheng Gang, Wu Jian Xin, Wu Yun Lin, Han Jun Song, Xiao Hua Sheng, Gao Heng Jun, Zhang Qing Hua

机构信息

State Key Laboratory of Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

J Dig Dis. 2007 Nov;8(4):186-93. doi: 10.1111/j.1751-2980.2007.00311.x.

Abstract

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 S100A6 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 S100A6 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.

摘要

目的

S100钙结合蛋白家族成员S100A6(钙周期蛋白)在多种恶性肿瘤中表达升高,但关于其在胃癌中的表达报道较少。本研究旨在探讨其在人胃癌及癌旁黏膜中的表达调控情况,以及在胃癌细胞系中对化疗药物的反应。

材料与方法

在一对匹配的胃癌样本中,进行基因表达系列分析(SAGE)实验,比较癌组织与癌旁组织的基因表达谱。为检测更多癌组织中的表达调控情况,进行了微阵列分析,并通过实时逆转录聚合酶链反应(RT-PCR)验证结果。在蛋白质水平,进一步采用蛋白质印迹法和组织芯片(TMA)检测来验证S100A6的表达。在SGC7901细胞系中,检测5-氟尿嘧啶和阿霉素对S100A6在mRNA和蛋白质水平的调控。

结果

采用SAGE策略,癌组织中鉴定出的S100A6标签比正常组织多5倍。通过cDNA微阵列分析,发现42例非选择性胃癌中有21例(50%)S100A6显著上调。在另外10对样本中,RT-PCR和蛋白质印迹分析也证实了S100A6的上调。共对14例内镜下取材的胃非癌性病变及相应的正常胃黏膜进行基因表达分析;cDNA微阵列和RT-PCR均显示S100A6在mRNA水平无显著变化。TMA检测显示,52例癌样本中有34例(65.4%)呈阳性染色,而80例非癌性病变中只有17例(21.3%)呈阳性,所有9例正常黏膜均为阴性。体外实验表明,在胃癌细胞系SGC-7901中,用5mg/L 5-氟尿嘧啶或0.3mg/L阿霉素处理后24至72小时,检测到S100A6 mRNA上调,且S100A6蛋白有两次上调。

结论

观察到的S100A6表达调控表明其与胃癌发生有关,S100A6定量检测是一种有前景的胃癌诊断工具。

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