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Involvement of p29/SYF2/fSAP29/NTC31 in the progression of NSCLC via modulating cell proliferation
Yifei Liu1, Tingting Ni2, Qun Xue3
1Department of Pathology, Affiliated Hospital of Nantong University, Nantong 226001, Jiangsu, China.
Abstract:
p29, also known as SYF2/fSAP29/NTC31, is a protein associated with chromatin and involved in DNA damage response, cell cycle arrest and pre-mRNA splicing. In p29-depleted cells, DNA replication was reduced and cell population in G1 phase increased. In this study, we investigated the potential role of p29 in the regulation of non-small cell lung cancer (NSCLC) progression. Western blot and immunohistochemistry staining showed that p29 was up-regulated in clinical NSCLC tissues compared with adjacent non-cancerous tissues, and the expression of p29 had a positive correlation with clinical stage and histological differentiation, as well as expression of Ki-67, a proliferating marker. Kaplan-Meier analysis indicated that patients with high level of p29 expression had poor overall survival. In addition, small interfering RNA of p29 was performed, and the effects on NSCLC growth were examined. Interference of p29 blocked S phase entry, inhibited proliferation of A549 cells and up-regulated level of p21 expression. Taken together, these results suggested that p29 might contribute to the progression of NSCLC by enhancing cell proliferation, implicating that targeting p29 might provide beneficial effects on the clinical therapy of NSCLC.
Insights
The protein p29 is elevated in non-small cell lung cancer (NSCLC) and promotes tumor growth by increasing cell proliferation. Targeting p29 may offer a new therapeutic strategy for NSCLC patients.
Area of Science:
- Molecular Biology
- Oncology
Background:
- p29 (SYF2/fSAP29/NTC31) is a chromatin-associated protein involved in DNA damage response, cell cycle arrest, and pre-mRNA splicing.
- p29 depletion leads to reduced DNA replication and increased G1 phase cell population.
Purpose of the Study:
- To investigate the role of p29 in the regulation of non-small cell lung cancer (NSCLC) progression.
Main Methods:
- Western blot and immunohistochemistry to analyze p29 expression in NSCLC tissues.
- Kaplan-Meier survival analysis.
- Small interfering RNA (siRNA) to interfere with p29 expression in A549 cells.
Main Results:
- p29 was significantly up-regulated in NSCLC tissues compared to adjacent non-cancerous tissues.
- p29 expression positively correlated with clinical stage, histological differentiation, and Ki-67 expression.
- High p29 levels were associated with poor overall survival in NSCLC patients.
- Interference of p29 blocked S phase entry, inhibited A549 cell proliferation, and increased p21 expression.
Conclusions:
- p29 contributes to NSCLC progression by enhancing cell proliferation.
- Targeting p29 may represent a potential therapeutic strategy for NSCLC.
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