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Aquarius® Solid Tumour probes

CHOP Breakapart Probe LPS015 - Detail

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.

Reference:/Bibliographie/Literatur/Bibliografia
  1. Enzingher and Weiss 1995 Soft Tissue Tumors Ed. 3. St Louis; C.V.Mosby
  2. Turc-Carel et al 1986 Can. Genet. Cytogenet. 23:291-299
  3. Mitelman 1995 Catalog of chromosome aberrations in cancer Ed. 5. New York: WileyLiss, Inc., 1994
  4. Antonescu et al 2000 Clin. Canc. Res. 7:3977-3987
  5. Ron and Habener 1992 Genes Dev., 6:439-453
  6. Crozat et al 1993 Nature, 363:640-444
  7. Rabbitts et al 1993 Nat. Genet., 4:175-180

Cytocell Aquarius

CHOP Breakapart Probe

Cat. No. LPS 015

CHOP Breakapart Probe

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