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Updated: Apr 1, 2026

Gene Regulation and Targeted Therapy in Gastric Cancer Peritoneal Metastasis: Radiological Findings from Dual Energy CT and PET/CT
Published on: January 22, 2018
Repression of PES1 expression inhibits growth of gastric cancer
Jieping Li1, Xiaodong Zhou2, Xiaopeng Lan3
1Department of Clinic Medical Laboratory, General Hospital of Fujian Corps of CAPF, Fuzhou, 350003, China. liejieping@hotmail.com.
Abstract:
Gastric cancer is one of the leading causes of cancer death worldwide. However, precise molecular mechanisms underlining its development are far from clear. We recently reported that PES1 promoted development of breast cancer and ovarian cancer as an oncogene. In this study, we reported that ablation of endogenous PES1 resulted in significant suppression of cell proliferation and growth and led to cell cycle arrest in G2 or G1 phase, respectively, in two gastric cancer cell lines (AGS and N87) in vitro. Meanwhile, silencing of PES1 obviously decreased expressions of cyclin D1, HIF-1α, and vascular endothelial growth factor (VEGF) expressions and increased p21WAF1 expression. Re-expression of PES1 in these two kinds of PES1 knockdown cells rescued these effects. In vivo, repression of endogenous PES1 expression suppressed gastric tumor growth in nude mice. In addition, 40.7 % (24/59) of gastric cancer tissues showed PES1 expression via immunohistochemical (IHC) staining. However, there were not any positive PES1 stainings in matched adjacent tissues. Our results demonstrated that repression of PES1 changed expressions of some cell proliferation- and angiogenesis-related genes and inhibited gastric cancer growth, and PES1 expression increased in gastric cancer tissues. These results suggest that PES1 may play an important role in development of gastric cancer. PES1 may be a potential target for gastric cancer therapy.
Insights
The oncogene PES1 drives gastric cancer growth by promoting cell proliferation and angiogenesis. Inhibiting PES1 suppressed tumor growth and may offer a new therapeutic target for gastric cancer.
Area of Science:
- Oncology
- Molecular Biology
Background:
- Gastric cancer is a leading cause of cancer mortality globally, with unclear molecular drivers.
- The oncogene PES1 has been implicated in breast and ovarian cancer development.
Purpose of the Study:
- To investigate the role of PES1 in gastric cancer development and progression.
- To explore PES1 as a potential therapeutic target for gastric cancer.
Main Methods:
- Investigated PES1 function in gastric cancer cell lines (AGS, N87) using gene silencing and re-expression.
- Analyzed cell proliferation, cell cycle, and gene expression (cyclin D1, HIF-1α, VEGF, p21WAF1).
- Evaluated PES1's effect on tumor growth in vivo using a nude mouse model and assessed PES1 expression in patient tissues via immunohistochemistry.
Main Results:
- Ablation of PES1 significantly suppressed gastric cancer cell proliferation, induced cell cycle arrest (G2/G1), and altered expression of key regulatory genes.
- PES1 knockdown decreased cyclin D1, HIF-1α, and VEGF, while increasing p21WAF1 expression.
- Repression of PES1 inhibited gastric tumor growth in vivo, and PES1 was overexpressed in gastric cancer tissues compared to adjacent normal tissues.
Conclusions:
- PES1 plays a significant role in gastric cancer development by influencing cell proliferation and angiogenesis.
- PES1 overexpression in gastric tumors suggests its potential as a diagnostic marker and therapeutic target for gastric cancer.
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