Gollin S M, Perrot L J, Gray B A, Kletzel M
Cancer Genet Cytogenet. 1986 Feb 15;20(3-4):331-9. doi: 10.1016/0165-4608(86)90092-0.
Cytogenetic analysis of a Ewing's sarcoma revealed a 46,XX,t(8;18)(q11;q21.3), t(11;22)(q23-24;q11-12) chromosome pattern. Observation of t(11;22) is consistent with other reported cases of Ewing's sarcoma. One breakpoint in this translocation, 11q23, coincides with the location of a folate-sensitive fragile site. Examination of peripheral blood leukocyte chromosomes from the patient revealed a 46,XX chromosome pattern with spontaneous, fluorodeoxyuridine-, and Bactrim-induced expression of fra(11)(q23). This may be the first demonstration of constitutional fra(11)(q23) expression in a patient with a neoplasm that exhibits a chromosome rearrangement involving this breakpoint and the first observation of spontaneous expression of this fragile site. These results provide a basis for discussion of the relationship between fragile sites and chromosome rearrangements.
对一例尤因肉瘤进行细胞遗传学分析,结果显示其染色体模式为46,XX,t(8;18)(q11;q21.3), t(11;22)(q23 - 24;q11 - 12)。观察到的t(11;22)与其他报道的尤因肉瘤病例一致。该易位中的一个断点11q23,与一个叶酸敏感脆性位点的位置重合。对该患者外周血白细胞染色体的检查显示其染色体模式为46,XX,且fra(11)(q23)有自发表达,以及经氟脱氧尿苷和复方新诺明诱导后的表达。这可能是首例在患有肿瘤且其染色体重排涉及该断点的患者中出现的体质性fra(11)(q23)表达,也是首次观察到该脆性位点的自发表达。这些结果为讨论脆性位点与染色体重排之间的关系提供了依据。