Characterization of add(I)(p36) in non-hodgkin lymphomas by fluorescence in situ hybridization
✍ Scribed by Svetlana Bajalica; Karen Brøndum-Nielsen; Anne-Grethe Sørensen; Niels Tinggaard Pedersen; Ulf Kristoffersson; Måns Åkerman; Margareta Anderson; Pavel Pisa; Magnus Nordenskjöld
- Book ID
- 102846830
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 538 KB
- Volume
- 13
- Category
- Article
- ISSN
- 1045-2257
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✦ Synopsis
Chromosome rearrangements involving chromosome I, band p36, are among the most common aberrations in non-Hodgkin lymphomas (NHL). We have studied nine cases of NHL with add( l)(p36) using fluorescence in situ hybridization (FISH) from a series of 205 cases. Five were follicular low-grade NHL and four were follicular or diffuse high-grade NHL. Three of the five cases with follicular low-grade NHL did not contain the 14;18 translocation. The extra material on the add(l)(p36) in these three cases was derived from chromosome segment 2q3 I -qter; in one it was observed as a sole clonal rearrangement. In the two remaining cases, with t( 14;18), the add( l)(p36) consisted of material from chromosome arms 3q and 17q, respectively. In the four cases of high-grade NHL, the material added on to I p36 was derived from chromosomes 6,9, 17, and 19, respectively.
Using a I p36-specific probe, D I S94, we showed a deletion on the add( I) in one of the cases with low-grade NHL, whereas no loss was observed in one of the cases with high-grade NHL. Our study indicates that cytogenetically similar add( l)(p36) are found in both high-and low-grade NHL, and the breakpoint on I p36 as well as the origin of translocated material may vary.
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## Abstract Aberrations of chromosomal bands 1p36 and 1q11–q23 are among the most common chromosomal alterations in non‐Hodgkin lymphoma (NHL). In this study, 16 cases of NHL showing recurrent unbalanced translocation t(1;1)(p36;q11–23) by G‐band analysis were selected for further analysis. To deli
Deletions of the long arm of chromosome 6 (6q) are among the most frequent chromosome aberrations in malignant lymphomas and often occur as secondary changes in addition to typical translocations, such as t(14;18). Using fluorescence in situ hybridization (FISH) with two YAC probes hybridizing to 6q