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Versican表达在胃腺癌中的预后意义

Prognostic significance of Versican expression in gastric adenocarcinoma.

作者信息

Shen X-H, Lin W-R, Xu M-D, Qi P, Dong L, Zhang Q-Y, Ni S-J, Weng W-W, Tan C, Huang D, Ma Y-Q, Zhang W, Sheng W-Q, Wang Y-Q, Du X

机构信息

Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China.

Clinical and Pathological Diagnosis Center, Ningbo, China.

出版信息

Oncogenesis. 2015 Nov 30;4(11):e178. doi: 10.1038/oncsis.2015.36.

Abstract

Gastric cancer (GC) is the leading malignancy in the digestive system. Versican is a ubiquitous component of the extracellular matrix and has a role in tumor progression. We aim to examine the expression of Versican in GC and the relationship between Versican levels and patient survival. We detected the mRNA expression of Versican in tumorous pairs and adjacent normal tissues (ANTs) of 78 GC patients by quantitative real-time polymerase chain reaction. The protein expression of Versican in 101 cases of matched GC and ANT, as well as in 27 intraepithelial neoplastic (IN) samples, was evaluated by immunohistochemistry. We analyzed the correlation between Versican levels and clinical outcomes. Finally, we performed CCK-8 cell counting assay and transwell assay in GC cell lines. Versican mRNA expression was significantly greater in tumor tissues (P<0.001) than in ANT. Versican was majorly expressed in the stroma surrounding tumor epithelium and minorly some areas of tumor epithelium. The Versican expression level was higher in GC than in ANT (P=0.004), but no significant difference was observed between ANT and IN (P=0.517). The Versican mRNA and protein levels were consistent in GC. High Versican mRNA and protein expression correlated with greater tumor invasion depth (P=0.030, P=0.027). Univariate and multivariate analysis revealed that patients with high Versican mRNA expression exhibited poor disease-specific survival (P<0.001). In vitro experiments showed that Versican overexpression promoted cell proliferation and invasion. Our data indicate that Versican may be a novel prognostic indicator in GC and may be a potential target for clinical diagnosis.

摘要

胃癌(GC)是消化系统中主要的恶性肿瘤。多功能蛋白聚糖是细胞外基质中广泛存在的成分,在肿瘤进展中起作用。我们旨在检测多功能蛋白聚糖在胃癌中的表达以及多功能蛋白聚糖水平与患者生存之间的关系。我们通过定量实时聚合酶链反应检测了78例胃癌患者肿瘤组织与癌旁正常组织(ANT)中多功能蛋白聚糖的mRNA表达。通过免疫组织化学评估了101例配对的胃癌和ANT组织以及27例上皮内瘤变(IN)样本中多功能蛋白聚糖的蛋白表达。我们分析了多功能蛋白聚糖水平与临床结局之间的相关性。最后,我们在胃癌细胞系中进行了CCK-8细胞计数实验和Transwell实验。多功能蛋白聚糖mRNA在肿瘤组织中的表达显著高于ANT(P<0.001)。多功能蛋白聚糖主要表达于肿瘤上皮周围的基质中,在肿瘤上皮的某些区域也有少量表达。胃癌中多功能蛋白聚糖的表达水平高于ANT(P=0.004),但ANT与IN之间未观察到显著差异(P=0.517)。胃癌中多功能蛋白聚糖的mRNA和蛋白水平一致。多功能蛋白聚糖mRNA和蛋白高表达与更大的肿瘤浸润深度相关(P=0.030,P=0.027)。单因素和多因素分析显示,多功能蛋白聚糖mRNA高表达的患者疾病特异性生存率较差(P<0.001)。体外实验表明,多功能蛋白聚糖过表达促进细胞增殖和侵袭。我们的数据表明,多功能蛋白聚糖可能是胃癌中一种新的预后指标,可能是临床诊断的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/678e/4670962/a5eb3ad582b3/oncsis201536f1.jpg

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