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P-Rex1 is required for efficient melanoblast migration and melanoma metastasis

Authors: Lindsay, Colin R.; Lawn, Samuel; Campbell, Andrew D.; Faller, William J.; Rambow, Florian; Mort, Richard L.; Timpson, Paul; +27 Authors

P-Rex1 is required for efficient melanoblast migration and melanoma metastasis

Abstract

Metastases are the major cause of death from melanoma, a skin cancer that has the fastest rising incidence of any malignancy in the Western world. Molecular pathways that drive melanoblast migration in development are believed to underpin the movement and ultimately the metastasis of melanoma. Here we show that mice lacking P-Rex1, a Rac-specific Rho GTPase guanine nucleotide exchange factor, have a melanoblast migration defect during development evidenced by a white belly. Moreover, these P-Rex1(-/-) mice are resistant to metastasis when crossed to a murine model of melanoma. Mechanistically, this is associated with P-Rex1 driving invasion in a Rac-dependent manner. P-Rex1 is elevated in the majority of human melanoma cell lines and tumour tissue. We conclude that P-Rex1 has an important role in melanoblast migration and cancer progression to metastasis in mice and humans.

Countries
United Kingdom, Netherlands
Keywords

Mice, Knockout, Cultured, Guanine Nucleotide Exchange Factors/genetics, Manchester Cancer Research Centre, Cells, Knockout, 610, In Vitro Techniques, Inbred C57BL, Immunohistochemistry, ResearchInstitutes_Networks_Beacons/mcrc; name=Manchester Cancer Research Centre, Melanoma/genetics, Mice, Inbred C57BL, Mice, Cell Movement, Tissue Array Analysis, Cell Movement/genetics, Animals, Guanine Nucleotide Exchange Factors, Humans, Neoplasm Metastasis, Neoplasm Metastasis/genetics, Melanoma, Cells, Cultured

  • BIP!
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    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    164
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 1%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 1%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
164
Top 1%
Top 10%
Top 1%
Green
gold
Related to Research communities
Cancer Research