Connective tissue growth factor and β-catenin constitute an autocrine loop for activation in rat sarcomatoid

Li Jiang1, Yoriko Yamashita, Shan-Hwu Chew

  • 1Department of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, Japan.

Insights

Connective tissue growth factor (Ctgf) drives aggressive sarcomatoid malignant mesothelioma (MM) by promoting proliferation and invasion. Ctgf is a potential biomarker and therapeutic target for this aggressive cancer.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • Malignant mesothelioma (MM) is a serious cancer linked to asbestos exposure.
  • Sarcomatoid MM (SM) is the most aggressive subtype with a poor prognosis.
  • Understanding the molecular drivers of SM is crucial for developing new treatments.

Purpose of the Study:

  • To identify genes contributing to the aggressiveness of sarcomatoid malignant mesothelioma (SM).
  • To investigate the role of connective tissue growth factor (Ctgf) in SM progression.
  • To explore Ctgf as a potential diagnostic and prognostic biomarker for MM.

Main Methods:

  • Induction of epithelioid (EM) and sarcomatoid (SM) MM in rats using asbestos.
  • Comparative transcriptome analysis between EM and SM subtypes.
  • Investigation of the Ctgf signaling pathway, including the β-catenin-TCF-LEF pathway and LRP6 receptor.

Main Results:

  • Ctgf expression was significantly elevated in SM compared to EM and normal mesothelium.
  • Ctgf drives SM proliferation and invasion via an autocrine β-catenin-TCF-LEF signaling loop.
  • High Ctgf expression correlated with epithelial-mesenchymal transition and serves as a serum biomarker in rats.

Conclusions:

  • Ctgf is a key regulator of aggressive sarcomatoid malignant mesothelioma.
  • The Ctgf-LRP6-GSK3β-β-catenin-TCF-Ctgf axis drives SM progression.
  • Ctgf represents a promising therapeutic target and diagnostic/prognostic biomarker for MM.

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