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S100A6对胃癌侵袭转移的调控机制研究

[Regulation mechanism study of S100A6 on invasion and metastasis in gastric cancer].

作者信息

Li Jun, Wang Xiao-hong, Li Zi-yu, Bu Zhao-de, Wu Ai-wen, Zhang Lian-hai, Wu Xiao-jiang, Zong Xiang-long, Ji Jia-fu

机构信息

Department of Gastrointestinal Cancer Surgery, Key Laboratory of Carcinogenesis and Translational Research(Ministry of Education), Peking University Cancer Hospital and Institute, Beijing 100142, China.

出版信息

Zhonghua Wei Chang Wai Ke Za Zhi. 2013 Nov;16(11):1096-101.

Abstract

OBJECTIVE

To detect the expression of S100A6 in gastric cancer, and to investigate the regulation mechanism of S100A6 in invasion and metastasis of gastric cancer.

METHODS

Expression of S100A6 protein in gastric cancer specimens, tissue adjacent to cancer, liver and lymph node metastasis tissue specimens was detected by immunohistochemical staining in 166 patients with gastric cancer from January 1995 to December 2001. Their association with clinicopathological factors was analyzed. Chromatin Immunoprecipitation-chip was used to detect the downstream factors potentially regulated by S100A6 in gastric cancer cell lines KATO3. S100A6 gene was transfected into gastric cancer cell line AGS, and cell invasion experiment and real time Q-polymerase chain reaction(RT Q-PCR) were used to detect the cell invasive ability and the mRNA expression of invasion-related factors (CDK5 and FLJ12438) in transfection group, negative control group and blank control group, respectively.

RESULTS

Low expression of S100A6 protein was found in cytoplasm of peritumoral tissues. In gastric cancer, liver and lymph node metastasis tissues, S100A6 protein expression was up-regulated in cytoplasm and (or) nuclei, especially in the tumor cells of invasive edge. The expression rates of gastric cancer, liver and lymph node metastasis tissues were 67.5%(112/166), 92.9%(26/28) and 100% (30/30) respectively. The high expression of S100A6 was associated with tumor local invasion, lymph node metastasis, cancer embolus, distant metastasis and TNM stages(all P<0.05). The transmembrane cell number was 31.3±5.5 in the S100A6 transfection group, significantly higher than that in negative control group (7.7±1.5) and blank control group (9.3±2.1)(both P<0.05), indicating an increase of cell invasion after S100A6 transfection. In transfection group, CDK5 mRNA expression was significantly higher than that in negative control group and blank control group(P<0.05). While FLJ1243 mRNA expression was similar among the three groups(P<0.05).

CONCLUSION

S100A6 may affect the malignant biological behavior of gastric cancer cells by regulating the expressions of down-stream invasion-associated factors, such as CDK5.

摘要

目的

检测S100A6在胃癌中的表达情况,并探讨其在胃癌侵袭和转移中的调控机制。

方法

采用免疫组化染色法检测1995年1月至2001年12月间166例胃癌患者的胃癌组织、癌旁组织、肝组织及淋巴结转移组织标本中S100A6蛋白的表达,分析其与临床病理因素的关系。运用染色质免疫沉淀芯片技术检测胃癌细胞系KATO3中可能受S100A6调控的下游因子。将S100A6基因转染至胃癌细胞系AGS中,分别采用细胞侵袭实验和实时荧光定量聚合酶链反应(RT Q-PCR)检测转染组、阴性对照组和空白对照组的细胞侵袭能力及侵袭相关因子(CDK5和FLJ12438)的mRNA表达。

结果

癌旁组织细胞质中S100A6蛋白表达较低。在胃癌组织、肝转移组织及淋巴结转移组织中,S100A6蛋白在细胞质和(或)细胞核中的表达上调,尤其是在侵袭边缘的肿瘤细胞中。胃癌组织、肝转移组织及淋巴结转移组织的表达率分别为67.5%(112/166)、92.9%(26/28)和100%(30/30)。S100A6高表达与肿瘤局部侵袭、淋巴结转移、癌栓、远处转移及TNM分期均相关(均P<0.05)。S100A6转染组的穿膜细胞数为31.3±5.5,显著高于阴性对照组(7.7±1.5)和空白对照组(9.3±2.1)(均P<0.05),表明S100A6转染后细胞侵袭能力增强。转染组中CDK5 mRNA表达显著高于阴性对照组和空白对照组(P<0.05)。而FLJ1243 mRNA表达在三组间差异无统计学意义(P>0.05)。

结论

S100A6可能通过调控下游侵袭相关因子如CDK5的表达来影响胃癌细胞的恶性生物学行为。

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