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1; 19 Translocation in human meningioma
Author(s) -
Prempree Thongbliew,
Amornmarn Rumpa,
Faillace Walter J.,
Arce Carlos A.,
Nguyen Tai Q.
Publication year - 1993
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19930401)71:7<2306::aid-cncr2820710722>3.0.co;2-s
Subject(s) - chromosomal translocation , karyotype , meningioma , chromosome , malignant meningioma , medicine , chromosome analysis , chromosome 22 , genetics , pathology , biology , gene
Background . Loss of chromosome 22 represents the most common chromosome abnormality (70%) in meningiomas. The remainder (30%) have a normal karyotype. Not only are the structural changes rare, they also occur simultaneously with various chromosome losses. Methods . The authors identified and studied the meningiomas of two patients with standard tumor cell culture technique and chromosome preparation. Results . Twenty karyotypes from each meningioma had a 46 modal chromosome number with t(1;19) (q21;p13) in all cells. Conclusions . The sole change of the (1;19) translocation in meningioma, without any other changes such as chromosome loss, as shown in this study, is unique and has never been reported before in the literature, to the knowledge of the authors. Additional study is needed to learn more about the rate of occurrence and the significant impact on meningeal tumor genesis.