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.

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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