KSR1 is coordinately regulated with Notch signaling and oxidative phosphorylation in thyroid cancer

Jandee Lee1, Mi-Youn Seol1, Seonhyang Jeong1

  • 1Departments of SurgeryInternal MedicinePathologyYonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, 120-752 Seoul, Korea.

Insights

Kinase suppressor of RAS1 (KSR1) plays a key role in papillary thyroid cancer (PTC) by upregulating Notch signaling and affecting mitochondrial oxidative phosphorylation. Targeting KSR1 may offer new therapeutic strategies for PTC.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cell Signaling

Background:

  • Kinase suppressor of RAS1 (KSR1) is a scaffold protein involved in RAS-mediated RAF activation.
  • The specific role of KSR1 in papillary thyroid cancer (PTC) has not been previously elucidated.

Purpose of the Study:

  • To characterize the molecular function and significance of KSR1 in papillary thyroid cancer (PTC).

Main Methods:

  • Quantitative real-time PCR (qRT-PCR) and immunohistochemistry (IHC) for KSR1 expression.
  • Gene Set Enrichment Analysis (GSEA) and GeneNetwork analysis for pathway associations.
  • siRNA-mediated KSR1 knockdown and subsequent molecular and cellular assays (e.g., ERK phosphorylation, Notch signaling targets, colony formation).
  • Electron microscopy for mitochondrial structure analysis.

Main Results:

  • KSR1 expression exhibits inter-tumor heterogeneity in PTC and is higher in BRAFV600E-positive tumors.
  • High KSR1 expression correlates with upregulated Notch signaling and downregulated oxidative phosphorylation (OxPhos) genes.
  • KSR1 knockdown reduces ERK phosphorylation, Notch signaling, and colony formation, while affecting mitochondrial structure.

Conclusions:

  • KSR1 is coordinately regulated with Notch signaling and oxidative phosphorylation in PTC.
  • KSR1's scaffold function may be crucial for sustaining proliferative signaling and metabolic reprogramming in PTC.
  • These findings suggest KSR1 as a potential therapeutic target in PTC.

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