Related Experiment Video
Updated: Jun 26, 2026

10:37
Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
Epithelial-Mesenchymal Transition Markers in Clear Cell Renal Cell Carcinoma: Expression Patterns and Prognostic
Lara Smoljo1, Tonka Mateljak1, Anita Racetin1,2
1Department of Anatomy, Histology and Embryology, Laboratory for Early Human Development, University of Split School of Medicine, Šoltanska 2A, 21000 Split, Croatia.
Journal of Personalized Medicine
|June 25, 2026
Summary
Protocadherin 9 (PCDH9) acts as a tumor suppressor in clear cell renal cell carcinoma (ccRCC), with its expression linked to better survival. ccRCC shows a partial epithelial-mesenchymal transition (EMT) phenotype, not a classical one.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genomics
Background:
- Clear cell renal cell carcinoma (ccRCC) is an aggressive kidney cancer subtype with poor prognosis.
- Epithelial-mesenchymal transition (EMT) is crucial for tumor progression, metastasis, and poor outcomes.
- The role of Protocadherin 9 (PCDH9) as a tumor suppressor and its relation to EMT markers in ccRCC are not well understood.
Purpose of the Study:
- To investigate the expression patterns of PCDH9, β-catenin (CTNNB1), Snail (SNAI1), and Vimentin (VIM) in ccRCC.
- To determine the prognostic significance of these markers in ccRCC patient survival.
- To explore the relationship between PCDH9 and EMT markers in ccRCC progression.
Main Methods:
- Immunofluorescence analysis on ccRCC tissue samples and adjacent normal renal cortex.
- Validation using The Cancer Genome Atlas (TCGA-KIRC) dataset via GEPIA2/GEPIA3 platforms.
- Differential expression, correlation, and survival analyses were performed.
Main Results:
- PCDH9 mRNA was downregulated, while Vimentin (VIM) was upregulated in ccRCC tumors.
- PCDH9 expression correlated positively with EMT markers (ZEB1, SNAI1) in tumors, unlike in normal tissue.
- High PCDH9 and CTNNB1 expression were associated with improved overall survival; VIM predicted progression, SNAI1 predicted mortality.
Conclusions:
- PCDH9 exhibits a tumor-suppressive role in ccRCC, with disrupted co-regulation of adhesion molecules.
- ccRCC displays a partial EMT phenotype, influencing tumor progression and patient outcomes.
- Endpoint-specific prognostic signatures (VIM, SNAI1, CTNNB1) can aid in patient stratification for ccRCC treatment.
