Basic Research
Copyright ©The Author(s) 2004. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Feb 1, 2004; 10(3): 393-399
Published online Feb 1, 2004. doi: 10.3748/wjg.v10.i3.393
Antiangiogenic effect of somatostatin receptor subtype 2 on pancreatic cancer cell line: Inhibition of vascular endothelial growth factor and matrix metalloproteinase-2 expression in vitro
Manoj Kumar, Zheng-Ren Liu, Laxmi Thapa, Qing Chang, Da-Yu Wang, Ren-Yi Qin
Manoj Kumar, Zheng-Ren Liu, Qing Chang, Da-Yu Wang, Ren-Yi Qin, Department of Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei Province, China
Laxmi Thapa, Department of Obstetrics and Gynecology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei Province, China
Author contributions: All authors contributed equally to the work.
Supported by National Natural Science Foundation of China, No. 30271473
Correspondence to: Manoj Kumar/Ren-Yi Qin, Department of Surgery, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, Hubei Province, China. ryqin@tjh.tjmu.edu.cn
Telephone: +86-27-83662389
Received: August 6, 2003
Revised: October 1, 2003
Accepted: October 7, 2003
Published online: February 1, 2004
Abstract

AIM: To investigate the anti-angiogenic effect of somatostatin receptor subtype 2 (SSTR2) gene transfer into pancreatic cancer cell line PC-3, and the mechanisms involved in this effect.

METHODS: The full length human SSTR2 cDNA was introduced into pancreatic cancer cell line PC-3 by lipofectamine-mediated transfection. Positive clones were screened by G418 and stable expression of SSTR2 was detected by immunohistochemistry SABC methods and RT-PCR. Enzyme-linked immunosorbent assay (ELISA) was used to detect vascular endothelial growth factor (VEGF) levels in the cell culture supernatants of SSTR2-expressing cells, vector control and mock control cells. Furthermore, the expressions of VEGF and matrix metalloproteinase-2 (MMP-2) were detected by immunohistochemistry SABC methods and RT-PCR in these cells.

RESULTS: VEGF levels in the cell culture supernatants were significantly reduced in the SSTR2-expressing cells (first week, 172.63 ± 21.2 ng/L and after two months, 198.85 ± 26.44 ng/L) compared with the vector control (first week, 790.39 ± 86.52 ng/L and after two months, 795.69 ± 72.35 ng/L) and mock control (first week, 786.42 ± 90.62 ng/L and after two months, 805.32 ± 84.36 ng/L) (P < 0.05). The immunohistochemical assay showed a significant reduction of the integral optical density of VEGF and MMP-2 in the SSTR2-expressing cells (42.25 ± 8.6 and 70.5 ± 6.25, respectively) compared with the vector control (85.75 ± 12.9 and 110.52 ± 13.5, respectively) and mock control (82.6 ± 9.28 and 113.56 ± 9.62, respectively) (P < 0.05). Conversely, the average gray value of VEGF and MMP-2 was significantly increased in the SSTR2-expressing cells (121.56 ± 8.43 and 134.46 ± 19.95, respectively) compared with the vector control (55.72 ± 5.6 and 62.26 ± 12.68, respectively) and mock control cells (58.48 ± 6.2 and 65.49 ± 9.16, respectively) (P < 0.05). Moreover, the expressions of VEGF mRNA and MMP-2 mRNA were significantly reduced in the SSTR2-expressing cells (0.1384 ± 0.017 and 0.2343 ± 0.070, respectively) compared with the vector control (1.024 ± 0.117 and 0.806 ± 0.119, respectively) and mock control (1.085 ± 0.105 and 0.714 ± 0.079, respectively) (P < 0.05).

CONCLUSION: The expression of reintroduced human SSTR2 gene exerts its antiangiogenic effects by down-regulating the expressions of the factors involved in tumor angiogenesis and metastasis, suggesting SSTR2 gene transfer as a new strategy of gene therapy for pancreatic cancer.

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