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Role of ARPC2 in Human Gastric Cancer
Jun Zhang1, Yi Liu2, Chang-Jun Yu2
1Department of General Surgery, Third Affiliated Hospital (Hefei First People's Hospital) of Anhui Medical University, Hefei, China.
Abstract:
Gastric cancer continues to be the second most frequent cause of cancer deaths worldwide. However, the exact molecular mechanisms are still unclear. Further research to find potential targets for therapy is critical and urgent. In this study, we found that ARPC2 promoted cell proliferation and invasion in the human cancer cell line MKN-28 using a cell total number assay, MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide) assay, cell colony formation assay, migration assay, invasion assay, and wound healing assay. For downstream pathways, CTNND1, EZH2, BCL2L2, CDH2, VIM, and EGFR were upregulated by ARPC2, whereas PTEN, BAK, and CDH1 were downregulated by ARPC2. In a clinical study, we examined the expression of ARPC2 in 110 cases of normal human gastric tissues and 110 cases of human gastric cancer tissues. ARPC2 showed higher expression in gastric cancer tissues than in normal gastric tissues. In the association analysis of 110 gastric cancer tissues, ARPC2 showed significant associations with large tumor size, lymph node invasion, and high tumor stage. In addition, ARPC2-positive patients exhibited lower RFS and OS rates compared with ARPC2-negative patients. We thus identify that ARPC2 plays an aneretic role in human gastric cancer and provided a new target for gastric cancer therapy.
Insights
Actin-related protein 2/3 complex subunit 2 (ARPC2) promotes gastric cancer growth and spread. Higher ARPC2 expression correlates with advanced disease and poorer survival, identifying it as a potential therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Research
Background:
- Gastric cancer is a leading cause of cancer mortality globally, with unclear molecular drivers.
- Identifying novel therapeutic targets is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the role of ARPC2 in gastric cancer progression.
- To explore ARPC2's downstream molecular pathways.
- To evaluate ARPC2 expression in clinical gastric cancer samples and its correlation with patient prognosis.
Main Methods:
- Utilized cell proliferation, migration, and invasion assays (MTT, colony formation, wound healing) in MKN-28 cells.
- Analyzed the expression of downstream genes regulated by ARPC2.
- Quantified ARPC2 expression in 110 gastric cancer tissues and 110 adjacent normal tissues via clinical study.
Main Results:
- ARPC2 significantly enhanced cell proliferation and invasion in vitro.
- ARPC2 modulated the expression of key cancer-related genes including CTNND1, EZH2, EGFR, PTEN, and CDH1.
- Elevated ARPC2 expression was observed in gastric tumors compared to normal tissues.
- ARPC2 levels correlated with larger tumor size, lymph node invasion, and advanced tumor stage.
- ARPC2-positive patients showed reduced relapse-free survival (RFS) and overall survival (OS).
Conclusions:
- ARPC2 plays a significant oncogenic role in human gastric cancer.
- ARPC2 represents a promising therapeutic target for gastric cancer treatment.
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