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Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
Epithelial-mesenchymal transition and its implications for fibrosis
Raghu Kalluri1, Eric G Neilson
1Center for Matrix Biology, Beth Israel Deaconess Medical Center, 330 Brookline Ave. (DANA 514), Boston, Massachusetts 02215, USA. rKalluri@BIDMC.Harvard.edu
The Journal of Clinical Investigation
|December 18, 2003
Summary
Epithelial to mesenchymal transition (EMT) drives cell diversity in development and fibrosis. This review explores EMT signaling in disease and its potential reversal by cytokines and growth factors.
Area of Science:
- Cell biology
- Developmental biology
- Pathology
Background:
- Epithelial to mesenchymal transition (EMT) is crucial for tissue development and cell diversification.
- While well-studied in embryonic development, EMT also contributes to fibroblast formation in adult organ fibrosis.
- In renal fibrosis, tubular epithelia can transform into disease-related fibroblasts.
Purpose of the Study:
- To review recent advances in understanding EMT signaling in both healthy and diseased states.
- To explore how cytokines and growth factors may modulate or reverse EMT.
- To highlight the role of EMT in organ fibrosis.
Main Methods:
- Literature review of recent studies on EMT signaling.
- Analysis of research on renal fibrosis and fibroblast origins.
- Synthesis of findings on cytokine and growth factor effects on EMT.
Main Results:
- EMT is a key process in embryonic development and adult tissue fibrosis.
- A significant portion of fibroblasts in renal fibrosis originate from tubular epithelia.
- Specific cytokines and growth factors show potential for attenuating or reversing EMT.
Conclusions:
- EMT is a fundamental biological process with implications in disease, particularly fibrosis.
- Targeting EMT pathways with specific factors offers therapeutic potential for fibrotic diseases.
- Further research into EMT reversal mechanisms is warranted for clinical applications.
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