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PGK1:一种胃癌腹膜播散的潜在标志物。

PGK1 a potential marker for peritoneal dissemination in gastric cancer.

作者信息

Zieker Derek, Königsrainer Ingmar, Traub Frank, Nieselt Kay, Knapp Bettina, Schillinger Christian, Stirnkorb Christian, Fend Falko, Northoff Hinnak, Kupka Susan, Brücher Björn L D M, Königsrainer Alfred

机构信息

Department of General, Visceral and Transplant Surgery, Comprehensive Cancer Center, Tuebingen, Germany.

出版信息

Cell Physiol Biochem. 2008;21(5-6):429-36. doi: 10.1159/000129635. Epub 2008 Apr 24.

DOI:10.1159/000129635
PMID:18453750
Abstract

BACKGROUND/AIMS: Peritoneal carcinomatosis, which is caused by the dissemination of cancer cells into the abdominal cavity is a frequent finding in patients with primary gastric cancer, and it is associated with a poor prognosis. The mechanisms that mediate peritoneal carcinomatosis in diffuse primary gastric tumours require definition.

METHODS

We therefore compared the gene expression profile in diffuse primary gastric cancer patients with and without peritoneal carcinomatosis (n=13). Human specimens from consecutive gastric cancer patients with and without peritoneal carcinomatosis were investigated using oligonucleotide microarrays. Differentially expressed genes of interest were further evaluated using quantitative real-time polymerase chain reaction (qRT-PCR).

RESULTS

The results reveal a significant overexpression of phosphoglycerate kinase 1 (PGK1), the chemokine CXCR4 and its ligand CXCL12 in specimens from diffuse gastric cancer patients with peritoneal carcinomatosis. Overexpression of PGK1 is known to increase the expression of CXCR4. CXCR4 on its part can increase CXCL12 expression. Elevated levels of CXCR4 and CXCL12 are associated with an increase in the metastatic rate and play an important role in the metastatic homing of malignant cells.

CONCLUSION

The overexpression of PGK1 and its signalling targets may be a expression-pathway in diffuse primary gastric carcinomas promoting peritoneal dissemination and may function as prognostic markers and/or be potential therapeutic targets to prevent the migration of gastric carcinoma cells into the peritoneum.

摘要

背景/目的:腹膜癌病是由癌细胞播散至腹腔引起的,在原发性胃癌患者中很常见,且与预后不良相关。弥漫性原发性胃肿瘤中介导腹膜癌病的机制尚需明确。

方法

因此,我们比较了有和没有腹膜癌病的弥漫性原发性胃癌患者(n = 13)的基因表达谱。使用寡核苷酸微阵列对连续的有和没有腹膜癌病的胃癌患者的人体标本进行研究。使用定量实时聚合酶链反应(qRT-PCR)进一步评估感兴趣的差异表达基因。

结果

结果显示,在有腹膜癌病的弥漫性胃癌患者的标本中,磷酸甘油酸激酶1(PGK1)、趋化因子CXCR4及其配体CXCL12有显著过表达。已知PGK1的过表达会增加CXCR4的表达。而CXCR4本身又能增加CXCL12的表达。CXCR4和CXCL12水平的升高与转移率的增加相关,并在恶性细胞的转移归巢中起重要作用。

结论

PGK1及其信号靶点的过表达可能是弥漫性原发性胃癌中促进腹膜播散的一条表达途径,可能作为预后标志物和/或成为预防胃癌细胞向腹膜迁移的潜在治疗靶点。

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