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Myxoid liposarcoma (MLS) is the most common subtype of liposarcoma1. The TLS-CHOP t(12;16)(q13;p11) fusion gene firstly described by Turc-Carel et al. in 19862, is now well established and present in at least 95% of MLS3. In rare cases a EWS-CHOP t(12;22)(q13;q12) translocation has been described4. The transcription factor gene, CHOP (DDIT3) (CREBPhomologous protein/DNA damage inducible transcript 3) is a negative regulator of adipocyte differentiation5. The TLS (Translocated in Liposarcoma)6 or FUS7 is a nuclear RNA-binding protein with extensive sequence similarity to EWS. The TLS-CHOP protein interferes with adipocyte differentiation and favours proliferation over terminal differentiation.
Cat. No. LPS 015
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