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Published on: May 29, 2017
Interplay between Podoplanin, CD44s and CD44v in Squamous Carcinoma Cells
Lucía Montero-Montero1, Jaime Renart1, Andrés Ramírez1
1Instituto de Investigaciones Biomédicas "Alberto Sols", Consejo Superior de Investigaciones Científicas (CSIC)-Universidad Autónoma de Madrid (UAM), 28029 Madrid, Spain.
Podoplanin and CD44 standard (CD44s) and variant (CD44v) isoforms are coordinately expressed in skin inflammation and cancer. This study reveals a physical interaction between podoplanin and CD44 isoforms, suggesting a functional interplay in squamous cell carcinoma.
Area of Science:
- Molecular biology
- Cancer research
- Cell biology
Background:
- Podoplanin and CD44 are transmembrane glycoproteins implicated in inflammation and cancer.
- Understanding their co-expression and interaction is crucial for elucidating mechanisms in carcinogenesis.
Purpose of the Study:
- To investigate the co-expression patterns of podoplanin with CD44 standard (CD44s) and variant (CD44v) isoforms in skin inflammation and chemical carcinogenesis.
- To determine the physical interaction between podoplanin and CD44 isoforms in squamous cell carcinoma (SCC) cells.
Main Methods:
- Analysis of co-expression in hyperplastic skin and various stages of mouse-skin chemical carcinogenesis.
- Immunofluorescence confocal microscopy to assess co-localization in SCC cell lines and in vivo.
- Co-immunoprecipitation assays to confirm physical binding between podoplanin and CD44 isoforms.
Main Results:
- Podoplanin is coordinately expressed with CD44s and specific CD44v isoforms (including CD44v10 in mice, and CD44v3-10, CD44v6-10, CD44v8-10 in humans) in SCCs.
- CD44v isoforms and CD44s co-localize with podoplanin at the plasma membrane of SCC cells.
- Podoplanin physically binds to CD44s and several CD44v isoforms, with interaction modulated by glycosylation.
Conclusions:
- A functional interplay exists between podoplanin and both CD44s and CD44v isoforms in SCC.
- The identified podoplanin-CD44 interaction provides insights into the regulation of their association in cancer progression.
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