Int J Med Sci 2020; 17(13):2040-2051. doi:10.7150/ijms.46774

Research Paper

Effect of gastric cancer stem cell on gastric cancer invasion, migration and angiogenesis

Zhipeng Zhu1*, Jiuhua Xu2*, Lulu Li1, Weipeng Ye2, Guoxing Xu3, Borong Chen1, Junjie Zeng1, Jiayi Li1, Zhengjie Huang1,2✉

1. Department of Gastrointestinal Surgery, Xiamen Cancer Center, The First Affiliated Hospital of Xiamen University, Xiamen (Fujian 361003), P.R. China.
2. Department of clinical medicine, Fujian Medical University, Fuzhou (Fujian 350004), P.R. China.
3. Endoscopy center, The First Affiliated Hospital of Xiamen University, Xiamen (Fujian 361003), P.R. China.
*These authors contributed equally to this work.

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Citation:
Zhu Z, Xu J, Li L, Ye W, Xu G, Chen B, Zeng J, Li J, Huang Z. Effect of gastric cancer stem cell on gastric cancer invasion, migration and angiogenesis. Int J Med Sci 2020; 17(13):2040-2051. doi:10.7150/ijms.46774. Available from http://www.medsci.org/v17p2040.htm

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Abstract

Purpose: Using the gastric cancer cell line SGC7901 and gastric cancer stem cell (CSC-G), we conducted this study to investigate the role of cancer stem cells in invasion, metastasis and tumor angiogenesis.

Methods: Stem cell markers (OCT4, SOX2, C-Myc and Klf4) expression was detected by RT-PCR and Western blotting. The proliferation, migration, invasion abilities, L-OHP and 5-FU resistance, angiogenesis were assessed using in vitro spherical clone formation assays, plate cloning experiments, transwell migration, transwell invasion, drug resistance, scratch-wound migration, ring formation assay, and their tumorigenic and ability were assessed using a tumor formation experiment in mice.

Results: Compared with the SGC7901, the expression of Oct4, Sox2, Klf4 and CD44 mRNA was significantly higher in CSC-G, the mRNA relative expression of E-cadherin in CSC-G was lower than SGC7901, while the expression of c-Myc did not significantly change. The proliferation, drug resistance, migration, and invasion abilities were significantly higher in CSC-G, and the tumorigenic ability in mice was also significantly higher.

Conclusion: The proliferation, drug resistance, migration, invasion, and tumorigenic abilities of CSC-G significantly were higher than SGC7901. CSC-G plays important roles in proliferation, migration, invasion, and tumorigenicity.

Keywords: Gastric cancer, Cancer stem cell, Tumor angiogenesis