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Updated: Feb 13, 2026

Establishment of Gastric Cancer Patient-derived Xenograft Models and Primary Cell Lines
Published on: July 19, 2019
The pseudogene-derived long non-coding RNA SFTA1P suppresses cell proliferation, migration, and invasion in gastric
Hongwei Ma1,2, Tianshi Ma1, Miao Chen2
1Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.
Abstract:
Pseudogenes were once regarded as transcriptionally inactive and without specific molecular function. However, current evidence shows that pseudogene-derived long non-coding RNAs (lncRNAs) may be crucial regulators of human cancer development, including gastric cancer (GC). In the present study, we report that a pseudogene-derived lncRNA named surfactant associated 1, pseudogene (SFTA1P), which is 693-nt long, was significantly down-regulated in GC tissues compared with that in the adjacent normal tissues. In addition, decreased SFTA1P expression was strongly correlated with advanced tumor lymph node metastasis (TNM) stage, larger tumor size, lymphatic metastasis, and poor prognosis of patients with GC. Moreover, gain-of-function experiments revealed that the overexpression of SFTA1P inhibits cell proliferation, migration, and invasion, thus verifying the tumor inhibitory role of SFTA1P in GC. Furthermore, we investigated the potential action mechanism of SFTA1P. Our results showed that down-regulation of SFTA1P may be associated with decreased TP53 expression. In summary, our work suggests that the pseudogene-derived lncRNA SFTA1P functions as a tumor suppressor in GC and thus may act as a potential diagnostic and therapeutic target of GC.
Insights
Pseudogene-derived long non-coding RNAs (lncRNAs) like SFTA1P are key in gastric cancer (GC). Decreased SFTA1P suppresses tumor growth and may serve as a diagnostic and therapeutic target for GC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Pseudogenes were historically considered non-functional.
- Emerging evidence highlights pseudogene-derived long non-coding RNAs (lncRNAs) as critical regulators in human cancers, including gastric cancer (GC).
Purpose of the Study:
- To investigate the role of the pseudogene-derived lncRNA SFTA1P in gastric cancer (GC).
- To explore SFTA1P as a potential diagnostic and therapeutic target for GC.
Main Methods:
- Quantitative real-time PCR to assess SFTA1P expression levels in GC tissues and adjacent normal tissues.
- Correlation analysis between SFTA1P expression and clinical parameters (TNM stage, tumor size, metastasis, prognosis).
- Gain-of-function experiments (overexpression) to evaluate the functional impact of SFTA1P on GC cell behavior (proliferation, migration, invasion).
- Investigation of the potential molecular mechanism involving TP53.
Main Results:
- SFTA1P was significantly down-regulated in GC tissues compared to normal tissues.
- Lower SFTA1P expression correlated with advanced TNM stage, larger tumor size, lymphatic metastasis, and poorer patient prognosis.
- Overexpression of SFTA1P inhibited GC cell proliferation, migration, and invasion.
- Down-regulation of SFTA1P was associated with decreased TP53 expression.
Conclusions:
- The pseudogene-derived lncRNA SFTA1P acts as a tumor suppressor in gastric cancer.
- SFTA1P represents a potential diagnostic biomarker and therapeutic target for GC.
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