Abstract
S1PR1 mutations are present in 7.8% of patients with MCL and are significantly more frequent at relapse.
S1PR1 mutations reduce expression of the S1PR1 receptor, which mediates migration towards the tissue-to-blood egress factor S1P in MCL.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Exons
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Gene Expression
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Genetic Association Studies*
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Genetic Predisposition to Disease*
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Humans
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Immunohistochemistry
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Lymphoma, Mantle-Cell / diagnosis*
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Lymphoma, Mantle-Cell / genetics*
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Mutation*
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Prognosis
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Receptors, Lysosphingolipid / genetics*
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Recurrence
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Sphingosine-1-Phosphate Receptors
Substances
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Receptors, Lysosphingolipid
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S1PR1 protein, human
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Sphingosine-1-Phosphate Receptors