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Updated: May 4, 2026

Yeast As a Chassis for Developing Functional Assays to Study Human P53
Published on: August 4, 2019
Phospholipase C ε-1 inhibits p53 expression in lung cancer
1Department of Cardiothoracic Surgery, Nanhai People's Hospital, the Nanfang Medical University Affiliated Nanhai Hospital, Foshan, China.
Abstract:
The pathogenesis of lung cancer is to be further investigated. Recent reports indicate that phospholipase C ε-1 (PLCE1) is a critical molecule involved in tumour growth. This study aims to investigate the role of PLCE1 in the regulation of apoptosis in lung cancer cells. In this study, the surgically removed non-small-cell lung cancer (NSCLC) tissue was collected from 36 patients. Single NSCLC cells were prepared from the tissue, in which immune cells of CD3(+) , CD11c(+) , CD19(+) , CD68(+) and CD14(+) were eliminated by magnetic cell sorting. The expression of PLCE1 and p53 was assessed by quantitative real-time polymerase chain reaction and Western blotting. Apoptosis of NSCLC cells was analysed by flow cytometry. The results showed that, in cultured NSCLC cells, high levels of PLCE1 and low levels p53 were detected; the two molecules showed a negative correlation (p < 0.01). The addition of anti-PLCE1 antibody increased the expression of p53 in NSCLC cells, which increased the frequency of apoptotic NSCLC cells. We conclude that NSCLC cells express high levels of PLCE1, which suppresses the expression of p53 in NSCLC cells. PLCE1 can be a therapeutic target of NSCLC.
Insights
Phospholipase C ε-1 (PLCE1) is highly expressed in non-small-cell lung cancer (NSCLC) cells, suppressing p53 expression and promoting tumor growth. Targeting PLCE1 may offer a new therapeutic strategy for NSCLC.
Area of Science:
- Oncology
- Molecular Biology
- Cell Biology
Background:
- Lung cancer pathogenesis requires further investigation.
- Phospholipase C ε-1 (PLCE1) is implicated in tumor growth.
- Understanding PLCE1's role in lung cancer apoptosis is crucial.
Purpose of the Study:
- To investigate the role of PLCE1 in regulating apoptosis in non-small-cell lung cancer (NSCLC) cells.
- To assess the correlation between PLCE1 and p53 expression in NSCLC.
- To evaluate PLCE1 as a potential therapeutic target for NSCLC.
Main Methods:
- Collected NSCLC tissue from 36 patients.
- Isolated NSCLC cells, removing immune cells via magnetic cell sorting.
- Assessed PLCE1 and p53 expression using quantitative real-time PCR and Western blotting.
- Analyzed NSCLC cell apoptosis via flow cytometry.
- Administered anti-PLCE1 antibody to assess its effect on p53 and apoptosis.
Main Results:
- High PLCE1 and low p53 levels were detected in cultured NSCLC cells.
- A significant negative correlation was observed between PLCE1 and p53 expression (p < 0.01).
- Anti-PLCE1 antibody treatment increased p53 expression and enhanced NSCLC cell apoptosis.
Conclusions:
- NSCLC cells exhibit high PLCE1 levels, which suppress p53 expression.
- PLCE1 negatively regulates p53, thereby inhibiting apoptosis in NSCLC.
- PLCE1 represents a potential therapeutic target for non-small-cell lung cancer.
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