Inhibitory effect of recombinant human semaphorin 3A on angiogenesis of gastric cancer and the associated mechanisms#br#

FENG Pin FAN Wen-jing LIU Lei XU Qian LI Yu-hong ZUO Yan-zhen ZHOU Bo ZHAO Xiang-yang

Acta Anatomica Sinica ›› 2020, Vol. 51 ›› Issue (2) : 220-227.

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Acta Anatomica Sinica ›› 2020, Vol. 51 ›› Issue (2) : 220-227. DOI: 10.16098/j.issn.0529-1356.2020.02.012
Cancer Biology

Inhibitory effect of recombinant human semaphorin 3A on angiogenesis of gastric cancer and the associated mechanisms#br#

  • FENG Pin1  FAN Wen-jing LIU Lei2  XU Qian3  LI Yu-hong4  ZUO Yan-zhen ZHOU Bo6  ZHAO Xiang-yang7*
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Abstract

Objective  To investigate the expression of semaphorin 3A (Sema3A) and its receptor neuropilin-1 (NRP-1) in gastric cancer and its correlation with microvessel density (MVD),and then to explore the effect of recombinant human Sema3A on angiogenesis of gastric cancer and the associated mechanisms.   Methods  Forty cases of gastric cancer tissues and its corresponding adjacent normal tissues were used to detecte the expression of Sema3A, NRP-1 and MVD in tissues by immunohistochemistry method . The expression level of Sema3A in serum of gastric cancer patient group and normal control group were measured by Enzyme-linked immuno-sorbent assay (ELISA). Western blotting was used to detect the expression of Sema3A and NRP-1 in five gastric cancer cell lines (MGC-803,HGC-27,MKN-28,SGC-7901,MKN-45) and human gastric mucosal epithelial cell (GES-1). Transwell chamber was used to construct non-contact in vitro co-culture system, in which the effects of different concentrations of recombinant human Sema3A on angiogenesis in gastric cancer were analyzed by tube formation assay preliminarily. The expression levels of vascular endothelial growth factor receptor 2 (VEGFR2) and NRP-1 in co-culture system were detected by Western blotting.   Results  The expression  levels of Sema3A in gastric cancer tissues, cell lines and patient serum were significantly lower than that in the control group(P<0.05), while the expression of NRP-1 in gastric cancer tissues and MKN-28 cells was significantly increased, and both of them were associated with TNM staging of gastric cancer(P<0.05). In vitro co-culture system, The tube forming abilities of human umbilical vein endothelial cell (HUVEC) were decreased in recombinant human Sema3A treated group, and this phenomenon was concentration dependent. The expression of VEGFR2 protein was down-regulated by recombinant human Sema3A.   Conclusion  The expression of Sema3A was decreased in gastric cancer tissues, cell lines and patient serum, and negatively correlated with microvessel density. The recombinant human Sema3A could inhibit the angiogenesis of gastric cancer in vitro, which may be related to down-regulation of VEGFR2 protein expression.

Key words

Gastric cancer /   / Semaphorin3A /   / Umbilical vein endothelial cell /   / Co-culture system / Tube formation assay /   / Western blotting /   / Human

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FENG Pin FAN Wen-jing LIU Lei XU Qian LI Yu-hong ZUO Yan-zhen ZHOU Bo ZHAO Xiang-yang. Inhibitory effect of recombinant human semaphorin 3A on angiogenesis of gastric cancer and the associated mechanisms#br#[J]. Acta Anatomica Sinica. 2020, 51(2): 220-227 https://doi.org/10.16098/j.issn.0529-1356.2020.02.012

References

[1] Liang D, Liang S, Jin J, et al. Gastric cancer burden of last 40 years in North China (Hebei Province): A population-based study[J]. Medicine (Baltimore), 2017,96(2):e5887.
[2] Chen LT, Oh DY, Ryu MH, et al. Anti-angiogenic therapy in patients with advanced gastric and gastroesophageal junction cancer: A Systematic Review[J]. Cancer Res Treat, 2017,49(4):851-868.
[3] Liang H. The 88th Annual Meeting of the Japanese Society of Gastric Cancer focus resolution [J]. Chinese Journal of Practical Surgery, 2016(6):641-643. (in Chinese)
梁寒. “第88届日本胃癌学会年会”焦点解析[J]. 中国实用外科杂志, 2016(6):641-643.
[4] Neufeld G, Mumblat Y, Smolkin T, et al. The role of the semaphorins in cancer[J]. Cell Adh Migr, 2016,10(6):652-674.
[5] Narazaki M, Tosato G. Ligand-induced internalization selects use of common receptor neuropilin-1 by VEGF165 and semaphorin3A[J]. Blood, 2006,107(10):3892-3901.
[6] Song X, Zhang W, Zhang Y, et al. Expression of semaphorin 3A and neuropilin 1 with clinicopathological features and survival in human tongue cancer[J]. Med Oral Patol Oral Cir Bucal, 2012,17(6):e962-e968.
[7] Wang Z, Chen J, Zhang W, et al. Axon guidance molecule semaphorin3A is a novel tumor suppressor in head and neck squamous cell carcinoma[J]. Oncotarget, 2016,7(5):6048-6062.
[8] Bussolino F, Giraudo E, Serini G. Class 3 semaphorin in angiogenesis and lymphangiogenesis[J]. Chem Immunol Allergy, 2014,99:71-88.
[9] Tang C, Gao X, Liu H, et al. Decreased expression of SEMA3A is associated with poor prognosis in gastric carcinoma[J]. Int J Clin Exp Pathol, 2014,7(8):4782-4794.
[10] Li L, Jiang X, Zhang Q, et al. Neuropilin-1 is associated with clinicopathology of gastric cancer and contributes to cell proliferation and migration as multifunctional co-receptors[J]. J Exp Clin Cancer Res, 2016,35(1):16.
[11] Zuazo-Gaztelu Ⅰ, Casanovas O. Unraveling the role of angiogenesis in cancer ecosystems[J]. Front Oncol, 2018,8:248.
[12] Xu R, Richards FM. Development of in vitro co-culture model in anti-cancer drug development Cascade[J]. Comb Chem High Throughput Screen, 2017,20(5):451-457.
[13] Li W, Khan M, Mao S, et al. Advances in tumor-endothelial cells co-culture and interaction on microfluidics[J]. J Pharm Anal, 2018,8(4):210-218.
[14] Miki Y, Ono K, Hata S, et al. The advantages of co-culture over mono cell culture in simulating in vivo environment[J]. J Steroid Biochem Mol Biol, 2012,131(3-5):68-75.
[15] Gonzalez-Gonzalez A, Gonzalez A, Alonso-Gonzalez C, et al. Complementary actions of melatonin on angiogenic factors, the angiopoietin/Tie2 axis and VEGF, in cocultures of human endothelial and breast cancer cells[J]. Oncol Rep, 2018,39(1):433-441.
[16] Huang C, Wang Y, Huang JH, et al. Sema3A drastically suppresses tumor growth in oral cancer Xenograft model of mice[J]. BMC Pharmacol Toxicol, 2017,18(1):55.
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