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Genomic imbalances during transformation from follicular lymphoma to diffuse large B-cell lymphoma

Berglund, Mattias (author)
Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi,Lymfomgruppen
Enblad, Gunilla (author)
Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi,Lymfomgruppen
Thunberg, Ulf (author)
Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi,Lymfomgruppen
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Amini, Rose-Marie (author)
Karolinska Institutet,Uppsala universitet,Institutionen för genetik och patologi
Sundström, Christer (author)
Uppsala universitet,Institutionen för onkologi, radiologi och klinisk immunologi
Roos, Göran (author)
Umeå universitet,Patologi
Erlanson, Martin (author)
Umeå universitet,Onkologi
Rosenquist, Richard (author)
Uppsala universitet,Institutionen för genetik och patologi
Larsson, Catharina (author)
Karolinska Institutet
Lagercrantz, Svetlana (author)
Karolinska Institutet
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 (creator_code:org_t)
Elsevier BV, 2007
2007
English.
In: Modern Pathology. - : Elsevier BV. - 0893-3952 .- 1530-0285. ; 20:1, s. 63-75
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Follicular lymphoma is commonly transformed to a more aggressive diffuse large B-cell lymphoma (DLBCL). In order to molecularely characterize this histiological and clinical transformation, comparative genomic hybridization was applied on 23 follicular lymphoma and 35 transformed DLBCL tumors from a total of 30 patients. The results were also compared with our published findings in de novo DLBCL. Copy number changes were detected in 70% of follicular lymphoma and in 97% of transformed DLBCL. In follicular lymphoma, the most common alterations were +18q21 (33%), +Xq25–26 (28%), +1q31–32 (23%), and -17p (23%), whereas transformed DLBCL most frequently exhibited +Xq25–26 (36%), +12q15 (29%), +7pter-q22 (25%), +8q21 (21%), and -6q16–21(25%). Transformed DLBCL showed significantly more alterations as compared to follicular lymphoma (P=0.0001), and the alterations -6q16–21 and +7pter-q22 were only found in transformed DLBCL but not in follicular lymphoma (P=0.02). Alterations involving +13q22 were significantly less frequent, whereas -4q13–21 was more common in transformed as compared to de novo DLBCL (P=0.01 and P=0.02, respectively). Clinical progression from follicular lymphoma to transformed DLBCL is on the genetic level associated with acquirement of increasing number of genomic copy number changes, with non-random involvement of specific target regions. The findings support diverse genetic background between transformed and de novo DLBCL.

Keyword

Comparative genomic hybridization
Lymphoma
Transformation
MEDICINE
MEDICIN

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art (subject category)

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