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Updated: Feb 22, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
The crosstalk between p38 and Akt signaling pathways orchestrates EMT by regulating SATB2 expression in NSCLC cells
Hakan Kucuksayan1, Hakan Akca1
1Department of Medical Biology, School of Medicine, Pamukkale University, Denizli, Turkey.
Abstract:
Epithelial-mesenchymal transition is a crucial event for metastasis and could be mediated by several pathways such as phosphoinositide 3-kinase/Akt, mitogen-activated protein kinases, as well as many epigenetic regulators. Special AT-rich sequence-binding protein 2 is an epigenetic regulator involved in epithelial-mesenchymal transition and osteoblastic differentiation. It has been reported that the crosstalk between several pathways is responsible for the regulation of epithelial-mesenchymal transition in cancer cells. However, crosstalks between p38 and Akt pathways involved in epithelial-mesenchymal transition are still unknown. We recently reported that there is a crosstalk between p38 and Akt pathways in non-small-cell lung carcinoma cells, and this crosstalk is associated with E-cadherin and special AT-rich sequence-binding protein 2 expressions. Therefore, we aimed to determine whether this crosstalk has a mediator role in the regulation of epithelial-mesenchymal transition in non-small-cell lung carcinoma. Our results showed that inhibition of p38 leads to the disruption of this crosstalk via decreased expression of phosphatase and tensin homolog (PTEN) and subsequently increased activation of Akt in non-small-cell lung carcinoma cells. Then, we found that p38 inhibition upregulated special AT-rich sequence-binding protein 2 expression and reversed epithelial-mesenchymal transition in non-small-cell lung carcinoma cells. Furthermore, special AT-rich sequence-binding protein 2 knockdown abolished the effect of p38 inhibition on epithelial-mesenchymal transition in non-small-cell lung carcinoma cells. In conclusion, our results strongly indicate that the crosstalk between p38 and Akt pathways can determine special AT-rich sequence-binding protein 2 expression and epithelial character of non-small-cell lung carcinoma cells, and special AT-rich sequence-binding protein 2 is a critical epigenetic regulator for epithelial-mesenchymal transition mediated by p38 pathway in non-small-cell lung carcinoma. Our findings will contribute to illuminate the molecular mechanisms of the epithelial-mesenchymal transition process that has a critical significance for lung cancer metastasis.
Insights
The p38 and Akt pathway crosstalk regulates epithelial-mesenchymal transition in lung cancer by controlling Special AT-rich sequence-binding protein 2. This epigenetic regulator is key to metastasis, offering new therapeutic targets.
Area of Science:
- Molecular oncology
- Cancer epigenetics
- Cellular signaling pathways
Background:
- Epithelial-mesenchymal transition (EMT) is vital for cancer metastasis, regulated by pathways like phosphoinositide 3-kinase/Akt and mitogen-activated protein kinases.
- Special AT-rich sequence-binding protein 2 (SATB2) is an epigenetic regulator implicated in EMT and cancer progression.
- The crosstalk between p38 and Akt pathways in EMT is not fully understood, particularly in non-small-cell lung carcinoma (NSCLC).
Purpose of the Study:
- To investigate the role of the crosstalk between p38 and Akt pathways in regulating EMT in NSCLC.
- To determine if SATB2 is a mediator in the p38/Akt pathway-driven EMT process in NSCLC.
Main Methods:
- Utilized non-small-cell lung carcinoma cell models.
- Investigated the effects of p38 inhibition on the p38/Akt pathway crosstalk, phosphatase and tensin homolog (PTEN) expression, and Akt activation.
- Assessed the impact of p38 inhibition on SATB2 expression and EMT markers.
- Performed SATB2 knockdown experiments to evaluate its role in mediating p38 inhibition effects on EMT.
Main Results:
- Inhibition of p38 disrupted the p38/Akt crosstalk by decreasing PTEN expression and increasing Akt activation.
- p38 inhibition led to upregulated SATB2 expression and reversed EMT in NSCLC cells.
- SATB2 knockdown abrogated the EMT-reversing effects of p38 inhibition, confirming SATB2's critical role.
Conclusions:
- The crosstalk between p38 and Akt pathways dictates SATB2 expression and the epithelial phenotype in NSCLC.
- SATB2 acts as a crucial epigenetic regulator mediating p38 pathway-driven EMT in NSCLC.
- These findings elucidate key molecular mechanisms of EMT in lung cancer metastasis and suggest potential therapeutic strategies targeting the p38/Akt/SATB2 axis.
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