Basic Research
Copyright ©2006 Baishideng Publishing Group Co., Limited. All rights reserved.
World J Gastroenterol. Jan 14, 2006; 12(2): 280-286
Published online Jan 14, 2006. doi: 10.3748/wjg.v12.i2.280
Expression of vascular endothelial growth factors A and C in human pancreatic cancer
Rui-Feng Tang, Shu-Xia Wang, Li Peng, Shun-Xiang Wang, Meng Zhang, Zhi-Feng Li, Zhi-Ming Zhang, Yan Xiao, Feng-Rui Zhang
Rui-Feng Tang, Li Peng, Shun-Xiang Wang, Meng Zhang, Zhi-Feng Li, Zhi-Ming Zhang, Yan Xiao, Feng-Rui Zhang, Department of Hepatobiliary Surgery, 4th Hospital, Hebei Medical University, Shijiazhuang 050011, Hebei Province, China
Shu-Xia Wang, Department of Dermatology, 4th Hospital, Hebei Medical University, Shijiazhuang 050011, Hebei Province, China
Supported by grant from Ministry of Education of China, No. 2002247
Correspondence to: Dr. Rui-Feng Tang, Department of Hepatobiliary Surgery, 4th Hospital, Hebei Medical University, 12 Jiankang Lu, Shijiazhuang 050011, Hebei Province, China. tangreifeng@163.com
Telephone: +86-311-86033941 ext 340
Received: June 15, 2005
Revised: June 28, 2005
Accepted: July 21, 2005
Published online: January 14, 2006
Abstract

AIM: To study the expression of vascular endothelial growth factor A (VEGF - A) and VEGF - C and to determine whether the presence of VEGF - A and VEGF - C was associated with the clinicopathologic characteristics of pancreatic cancer.

METHODS: VEGF - A and VEGF - C mRNA transcripts were examined by Northern blot in 6 human pancreatic cancer cell lines and 8 normal pancreatic tissues and 8 pancreatic carcinoma specimens. The expression of VEGF - A and VEGF - C proteins was examined by Western blot in the tested cell lines and by immunohistochemical stain in 50 pancreatic carcinoma samples.

RESULTS: VEGF - A and VEGF - C mRNA transcripts were present in all the 6 human pancreatic cancer cell lines. Immunoblotting revealed the presence of VEGF - A and VEGF - C proteins in all the cell lines. Northern blot analysis of total RNA revealed 3.0-fold and 3.6 - fold increase in VEGF - A and VEGF - C mRNA transcript in the cancer samples, respectively. Immunohistochemical analysis confirmed the expression of VEGF - A and VEGF - C in cancer cells within the tumor mass. Immunohistochemical analysis of 50 pancreatic cancer tissue samples revealed the presence of VEGF-A and VEGF - C immunoreactivity in 50% and 80% of the cancer tissue samples, respectively. The presence of VEGF-A in these cells was associated with larger tumor size and enhanced local spread (χ2 = 6.690, P = 0.035<0.05) but was not associated with decreased patient survival. However, the presence of VEGF-C in the cancer cells was associated with increased lymph node metastasis (χ2 = 5.710, P  = 0.017<0.05), but was not associated with decreased patient survival. There was no correlation between the expression of VEGF - A and VEGF - C in the same cancer cells.

CONCLUSION: VEGF - A and VEGF-C are commonly overexpressed in human pancreatic cancer and may contribute to tumor growth and lymph node metastasis. There is no relationship between the expression of VEGF - A and VEGF - C in pancreatic cancer.

Keywords: Pancreatic cancer; Vascular endothelial growth factor - A; Vascular endothelial growth factor - C; Survival