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Combined Conditional Knockdown and Adapted Sphere Formation Assay to Study a Stemness-Associated Gene of Patient-derived Gastric Cancer Stem Cells
Published on: May 9, 2020
KCNE2, a down-regulated gene identified by in silico analysis, suppressed proliferation of gastric cancer cells
Pan Yanglin1, Zhao Lina, Liu Zhiguo
1State Key Laboratory of Cancer Biology and Institute of Digestive Diseases, Xijing Hospital, The Fourth Military Medical University, Xi'an, Shaanxi Province, PR China.
Abstract:
It is important to identify the differentially expressed gene in gastric cancer for elucidating the molecular mechanisms of tumorigenesis of stomach. Here, 38 genes differentially expressed genes between gastric cancer and normal gastric mucosa by in silico approaches. A potassium channel protein KCNE2, identified as a down-regulated gene in gastric cancer, was chosen for further study. We investigated the expression of KCNE2 in gastric cancer tissues and cell lines and examined the effect of KCNE2 on proliferation of gastric cancer. The expression of KCNE2 was markedly down-regulated in gastric cancer tissues and cell lines. Forced overexpression of KCNE2 suppressed the growth of SGC7901 cells and cell cycle progression significantly, which might be related to the down-regulation of Cyclin D1. KCNE2 also inhibited SGC7901 cell growth in soft agar and its tumorigenicity in nude mice. Taken together, our work showed that in silico analysis approaches could be used to identify cancer-related genes effectively. KCNE2, as a novel down-regulated gene in gastric cancer, suppressed cell proliferation and tumorigenesis of stomach.
Insights
Identifying key genes in stomach cancer is crucial. This study found that KCNE2 (potassium channel protein) is down-regulated in gastric cancer and suppresses tumor growth and proliferation.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Gastric cancer (stomach cancer) pathogenesis involves complex molecular alterations.
- Identifying differentially expressed genes is vital for understanding tumorigenesis and finding therapeutic targets.
Purpose of the Study:
- To identify novel genes involved in gastric cancer development using in silico methods.
- To investigate the role of the down-regulated potassium channel protein KCNE2 in gastric cancer progression.
Main Methods:
- In silico analysis to identify 38 differentially expressed genes between gastric cancer and normal tissues.
- Investigated KCNE2 expression in gastric cancer tissues and cell lines.
- Examined the effect of KCNE2 overexpression on gastric cancer cell proliferation, cell cycle, soft agar colony formation, and in vivo tumorigenicity.
Main Results:
- KCNE2 expression was significantly down-regulated in gastric cancer tissues and cell lines.
- Forced overexpression of KCNE2 suppressed SGC7901 cell proliferation and cell cycle progression, potentially via down-regulation of Cyclin D1.
- KCNE2 inhibited SGC7901 cell growth in soft agar and reduced tumor formation in nude mice.
Conclusions:
- In silico approaches are effective for identifying cancer-related genes.
- KCNE2 acts as a tumor suppressor in gastric cancer by inhibiting cell proliferation and tumorigenesis.
- KCNE2 represents a potential novel therapeutic target for stomach cancer.
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