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Updated: Feb 8, 2026

Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion
Published on: April 2, 2020
Decreased expression of TROAP suppresses cellular proliferation, migration and invasion in gastric cancer
Ke Jing1, Qinsheng Mao1, Peng Ma1
1Department of Gastrointestinal Surgery, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, P.R. China.
Abstract:
Trophinin associated protein (TROAP) is a cytoplasmic protein required for spindle assembly and cell invasion; however, its biological function in cancer remains to be elucidated. In the present study, by analyzing three independent datasets from the Oncomine database, it was identified that TROAP mRNA expression was upregulated in gastric cancer (GC) tissues compared with normal counterparts. Furthermore, elevated expression of TROAP was associated with poor survival in patients with GC, as predicted using Kaplan‑Meier analysis. TROAP was knocked down to verify its functional role in gastric cancer cell lines, SGC‑7901 and MGC80‑3. MTT assay was used to analyze cell proliferation. Cell cycle progression, and migration and invasion were determined using flow cytometry and Transwell assay, respectively. In vitro experiments demonstrated that knockdown of TROAP significantly suppressed cell proliferation, G1 to S cell cycle transition, and the migration and invasion ability of GC cells. The results of the present study suggest that TROAP is overexpressed in GC and serves an oncogenic role in gastric cancer by affecting cell proliferation and invasion.
Insights
Trophinin associated protein (TROAP) is upregulated in gastric cancer, promoting cell proliferation and invasion. Knocking down TROAP suppressed these oncogenic behaviors, suggesting it as a potential therapeutic target for gastric cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Trophinin associated protein (TROAP) is a cytoplasmic protein involved in spindle assembly and cell invasion.
- The specific role of TROAP in cancer development and progression is not fully understood.
Purpose of the Study:
- To investigate the expression and function of TROAP in gastric cancer (GC).
- To determine the potential of TROAP as a prognostic marker and therapeutic target in GC.
Main Methods:
- Analysis of TROAP mRNA expression in GC tissues using Oncomine database.
- Kaplan-Meier survival analysis to correlate TROAP expression with patient outcomes.
- In vitro experiments involving TROAP knockdown in GC cell lines (SGC-7901, MGC80-3).
- Assessment of cell proliferation (MTT assay), cell cycle progression (flow cytometry), and migration/invasion (Transwell assay).
Main Results:
- TROAP mRNA expression was significantly upregulated in gastric cancer tissues compared to normal tissues.
- Elevated TROAP expression was associated with poorer survival rates in GC patients.
- Knockdown of TROAP inhibited GC cell proliferation, suppressed G1 to S phase transition, and reduced migration and invasion capabilities.
Conclusions:
- TROAP is overexpressed in gastric cancer and plays a significant oncogenic role.
- TROAP promotes gastric cancer cell proliferation and invasion, indicating its potential as a therapeutic target.
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