VEGF-A and VEGF-B mRNA expression in gastro-oesophageal cancers

被引:6
|
作者
Angelescu, Cristina [1 ,2 ]
Burada, Florin [1 ,2 ]
Ioana, Mihai [1 ,2 ]
Angelescu, Radu [2 ,3 ]
Moraru, Emil [4 ]
Riza, Anca [1 ]
Marchian, Sanda [5 ]
Mixich, Francisc [1 ,2 ]
Cruce, Mihai [1 ]
Saftoiu, Adrian [2 ,3 ]
机构
[1] Univ Med & Pharm Craiova, Lab Human Genom, Craiova, Romania
[2] Univ Med & Pharm Craiova, Res Ctr Gastroenterol & Hepatol, Craiova, Romania
[3] Univ Med & Pharm Craiova, Dept Internal Med, Craiova, Romania
[4] Univ Med & Pharm Craiova, Dept Gen Surg, Craiova, Romania
[5] Lucian Blaga Univ, Fac Med Victor Papilian, Sibiu, Romania
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2013年 / 15卷 / 04期
关键词
Gastro-oesophageal cancer; VEGF-A; VEGF-B; Isoform; qRT-PCR; ENDOTHELIAL GROWTH-FACTOR; GASTRIC-CANCER; MICROVESSEL DENSITY; POLYMORPHISMS; ANGIOGENESIS; ISOFORMS; TUMORS; BEVACIZUMAB; VEGF(165)B; CARCINOMA;
D O I
10.1007/s12094-012-0923-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Angiogenesis is essential for the local growth, invasion and metastasis of the tumours. Vascular endothelial growth factors (VEGFs) play a crucial role in tumour angiogenesis. The aim of our study was to quantify the expression of several VEGF family molecules in human gastro-oesophageal cancers and to analyse possible correlations between genes expression and clinico-pathological features. Gene expression was quantified in 43 gastro-oesophageal paired samples using qRT-PCR with TaqMan probes specific to VEGF-A, including soluble transcript variants and VEGF-B genes. VEGF-A, including the studied splice variants and VEGF-B mRNAs were expressed in both tumour and peritumour mucosa. The expression of VEGF-A and its isoforms was higher in tumour compared with paired peritumour mucosa, while no significant difference was observed in VEGF-B expression. VEGF-A expression tended to correlate with tumour invasion. VEGF-A has a tendency to over-express in gastro-oesophageal cancers, while VEGF-B does not seem involved in these tumours. Further studies are required to establish the utility of anti-VEGF-A therapy and to find biomarkers for pathogenesis or response to therapy in gastro-oesophageal tumours.
引用
收藏
页码:313 / 320
页数:8
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