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EGR1/2 Inhibits Papillary Thyroid Carcinoma Cell Growth by Suppressing the Expression of PTEN and BAX
1Department of General Surgery, The Second Hospital of Hebei Medical University, No. 215 Heping West Road, Shijiazhuang, 050000, Hebei, China.
Abstract:
Early growth response (EGR) proteins have been reported to be involved in cell growth and apoptosis in a variety of cancer types and could inhibit tumor development. However, the role of EGR1/2 in papillary thyroid carcinoma (PTC) has not been elucidated. The expression pattern of EGR1/2 in adjacent tissues and cancer tissues and the clinical prognosis of EGR1/2 were analyzed by using the samples from TCGA database. The cell viability was detected by MTT assay. Luciferase reporter assay was used to demonstrate the binding of EGR1/2 to the target gene promotor region. Our results showed that EGR1/2 was significantly downregulated in tumor tissues and correlated with poor prognosis. Overexpression of EGR1/2 inhibited proliferation of IHH-4 and BCPAP cells, and knockdown of EGR1/2 showed a reverse effect. Overexpression of EGR1 or EGR2 promoted phosphatase and tension homolog (PTEN) or Bcl-2-associated X (BAX) expression, and EGR1 or EGR2 was able to directly bind to the promoter region of PTEN or BAX. In conclusion, we found that the altered expression of EGR1/2 affected the proliferation of PTC cells and regulated the expression of PTEN and BAX.
Insights
Early Growth Response (EGR) 1 and 2 proteins are downregulated in papillary thyroid carcinoma (PTC), correlating with poor prognosis. Upregulating EGR1/2 inhibits PTC cell proliferation by modulating PTEN and BAX expression.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Early Growth Response (EGR) proteins are implicated in cell growth and apoptosis across various cancers.
- The specific role of EGR1 and EGR2 in papillary thyroid carcinoma (PTC) remains unclear.
- Understanding EGR1/2 function in PTC is crucial for potential therapeutic strategies.
Purpose of the Study:
- To investigate the expression patterns and prognostic significance of EGR1/2 in papillary thyroid carcinoma.
- To determine the effect of EGR1/2 on PTC cell proliferation.
- To elucidate the molecular mechanisms by which EGR1/2 influences PTC progression, including target gene regulation.
Main Methods:
- Analysis of EGR1/2 expression and clinical prognosis using The Cancer Genome Atlas (TCGA) database.
- Cell viability assays (MTT) to assess the impact of EGR1/2 on PTC cell proliferation.
- Luciferase reporter assays to confirm direct binding of EGR1/2 to target gene promoter regions.
Main Results:
- EGR1/2 expression was significantly downregulated in PTC tumor tissues compared to adjacent tissues.
- Lower EGR1/2 expression correlated with a poorer clinical prognosis in PTC patients.
- Overexpression of EGR1/2 inhibited proliferation in IHH-4 and BCPAP PTC cell lines, while knockdown enhanced it.
- EGR1 or EGR2 overexpression led to increased expression of phosphatase and tension homolog (PTEN) or Bcl-2-associated X (BAX).
- Direct binding of EGR1 or EGR2 to the promoter regions of PTEN or BAX was confirmed.
Conclusions:
- EGR1/2 are significantly downregulated in papillary thyroid carcinoma and are associated with unfavorable prognosis.
- Altered EGR1/2 expression impacts PTC cell proliferation.
- EGR1/2 regulate PTC cell proliferation through modulation of PTEN and BAX expression.
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