التفاصيل البيبلوغرافية
| العنوان: |
TRPA1 Expression in Synovial Sarcoma May Support Neural Origin. |
| المؤلفون: |
De Logu, Francesco, Ugolini, Filippo, Caporalini, Chiara, Palomba, Annarita, Simi, Sara, Portelli, Francesca, Campanacci, Domenico Andrea, Beltrami, Giovanni, Massi, Daniela, Nassini, Romina |
| المصدر: |
Biomolecules (2218-273X); Oct2020, Vol. 10 Issue 10, p1446-1446, 1p |
| مصطلحات موضوعية: |
SYNOVIOMA, SOFT tissue tumors, MULTIPOTENT stem cells, SENSORY neurons, NEUROGLIA, MESENCHYMAL stem cells, NEURAL stem cells, OLIGODENDROGLIA |
| مستخلص: |
Synovial sarcoma (SS) is a malignant mesenchymal soft tissue neoplasm. Despite its name, the cells of origin are not synovial cells, but rather neural, myogenic, or multipotent mesenchymal stem cells have been proposed as possible cells originators. Unlike other sarcomas, an unusual presentation of long-term pain at the tumor site has been documented, but the exact mechanisms have not been fully clarified yet. The transient receptor potential ankyrin 1 (TRPA1) is a nonselective cation channel mainly expressed in primary sensory neurons, where it functions as a pain sensor. TRPA1 have also been described in multiple non-excitable cells, including those derived from neural crest stem cells such as glial cells and, in particular, Schwann cell oligodendrocytes and astrocytes. We evaluated TRPA1 expression in SS. We selected a cohort of 41 SSs, and by immunohistochemistry, we studied TRPA1 expression. TRPA1 was found in 92.6% of cases. Triple TRPA1/pS100/SOX10 and TRPA1/SLUG/SNAIL staining strongly supports a neural origin of SS. TRPA1 positivity was also observed in a subset of cases negative with pS100, SOX10 and/or SLUG/SNAIL, and these divergent phenotypes may reflect a process of tumor plasticity and dedifferentiation of neural-derived SSs. Given the functional diversity of TRPA1 and its expression in neuronal and non-neuronal multipotent neural crest stem cells, it remains to be determined whether TRPA1 expression in SSs neoplastic cells plays a role in the molecular mechanism associated with premonitory pain symptoms and tumor progression. [ABSTRACT FROM AUTHOR] |
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