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Tumor microenvironment modulates hyaluronan expression: the lactate effect
Sri Rajalakshmi Rudrabhatla1, Christie L Mahaffey, Mark E Mummert
1Department of Dermatology, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
The Journal of Investigative Dermatology
|March 18, 2006
Summary
Melanoma cells
Area of Science:
- Oncology
- Biochemistry
- Cell Biology
Background:
- Hyaluronan (HA) synthesis is regulated by the microenvironment, influencing melanoma cell growth and metastasis.
- High HA-producing melanoma cells show increased tumor growth and metastatic potential.
- Previous studies primarily examined HA expression in vitro, necessitating in vivo investigation.
Purpose of the Study:
- To compare hyaluronan expression patterns in B16-F1 and B16-F10 melanoma cells in vitro and in situ.
- To investigate the role of the tumor microenvironment, specifically lactate, in regulating HA synthesis in melanoma cells.
Main Methods:
- Assessed cell surface HA expression using the HA-binding peptide Pep-1.
- Compared HA expression in B16-F1 and B16-F10 cells both in vitro and in situ using cryostat sections.
- Investigated the effect of lactate stimulation on HA expression in both cell lines.
Main Results:
- B16-F1 melanoma cells exhibited significantly higher Pep-1 binding (indicating higher HA levels) in vitro compared to B16-F10 cells.
- In situ, HA expression levels were comparable between B16-F1 and B16-F10 cells within skin tumors.
- Lactate stimulation induced high HA concentrations in B16-F10 cells but not in B16-F1 cells.
Conclusions:
- B16-F1 cells show high HA expression both in vitro and in vivo.
- B16-F10 cells express high HA concentrations primarily within the tumor microenvironment, particularly after lactate stimulation.
- Tumor microenvironment components like lactate can induce HA expression in melanoma cells, potentially promoting an aggressive phenotype.