Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.
Author(s) -
Claude TurcCarel,
Paola Dal Cin,
Janusz Limon,
Uma Rao,
F P Li,
Joseph M. Corson,
Rebekah Zimmerman,
Dilys M. Parry,
Janet M. Cowan,
A.A. Sandberg
Publication year - 1987
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.84.7.1981
Subject(s) - chromosomal translocation , synovial sarcoma , biology , sarcoma , karyotype , chromosome , x chromosome , cytogenetics , microbiology and biotechnology , pathology , genetics , medicine , gene
A translocation that involves chromosome X (band p11.2) and chromosome 18 (band q11.2) was observed in short-term in vitro cultures of cells from five synovial sarcomas and one malignant fibrous histiocytoma. In four of these tumors, the translocation t(X;18)(p11.2;q11.2) was reciprocal. The two other tumors had complex translocations: t(X;18;21)(p11.2;q11.2;p13) and t(X;15;18)(p11.2;q23;q11.2). A translocation between chromosomes X and 18 was not detected in other histological types of soft tissue sarcoma. The X;18 rearrangement appears to characterize the synovial sarcoma and is the first description of a primary, nonrandom change in the sex chromosome of a human solid tumor.
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