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Related Experiment Video

Updated: May 20, 2026

Induction of Mesenchymal-Epithelial Transitions in Sarcoma Cells
11:42

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Published on: April 7, 2017

Protons sensitize epithelial cells to mesenchymal transition.

Minli Wang1, Megumi Hada, Janapriya Saha

  • 1Division of Space Life Sciences, Universities Space Research Association, Houston, Texas, United States of America.

Plos One
|July 31, 2012
PubMed
Summary

Low energy protons, encountered in space and proton radiotherapy, can enhance epithelial-mesenchymal transition (EMT) in cells. This process, crucial for tumor invasion, is amplified by protons, especially when combined with TGFβ1 signaling.

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Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
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Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells

Published on: October 27, 2020

Area of Science:

  • Cell biology
  • Radiation oncology
  • Space medicine

Background:

  • Proton radiotherapy is increasingly used for deep-seated tumors.
  • Astronauts are exposed to space radiation, including protons.
  • The cancer risk associated with proton exposure is not well understood.

Purpose of the Study:

  • To investigate the biological effects of low energy protons on epithelial cells.
  • To determine if protons enhance transforming growth factor beta 1 (TGFβ1)-mediated epithelial-mesenchymal transition (EMT).
  • To understand EMT's role in tumor progression, invasion, and metastasis.

Main Methods:

  • Utilized mink lung epithelial cells (Mv1Lu) and human esophageal epithelial cells (EPC).
  • Assessed EMT through morphological changes, gene expression (real-time PCR), and protein markers (immunostaining, western blotting).
  • Investigated the effects of low energy protons (5 MeV) and TGFβ1, using a TGFβR1 inhibitor (SD208).

Main Results:

  • Low energy protons (0.1 Gy) enhanced TGFβ1-induced EMT in both cell types.
  • Protons alone induced a mild EMT.
  • The TGFβR1 inhibitor SD208 effectively blocked TGFβ1/Smad signaling and attenuated EMT.

Conclusions:

  • Low and high doses of protons can sensitize epithelial cells to EMT.
  • Proton-enhanced EMT is more prominent with TGFβ1 but also occurs independently.
  • A model for proton-induced EMT in normal and cancerous tissues is proposed.