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Upregulation of bfl-1 is a potential mechanism of chemoresistance in B-cell chronic lymphocytic leukaemia

Olsson, A. (author)
Karolinska Institutet
Norberg, Maria (author)
Uppsala universitet,Institutionen för genetik och patologi
Ökvist, A. (author)
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Derkow, K. (author)
Choudhury, A. (author)
Karolinska Institutet
Tobin, Gerard (author)
Uppsala universitet,Institutionen för genetik och patologi
Celsing, F. (author)
Österborg, A. (author)
Karolinska Institutet
Rosenquist, Richard (author)
Uppsala universitet,Institutionen för genetik och patologi
Jondal, M. (author)
Karolinska Institutet
Osorio, L. M. (author)
Karolinska Institutet
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 (creator_code:org_t)
2007-08-28
2007
English.
In: British Journal of Cancer. - : Springer Science and Business Media LLC. - 0007-0920 .- 1532-1827. ; 97:6, s. 769-777
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • B-cell chronic lymphocytic leukaemia (B-CLL) is characterised by the progressive accumulation of monoclonal CD5+ B cells. In a previous study, we have analysed the expression profile of apoptosis-regulating genes using a cDNA-based microarray and found overexpression of the antiapoptotic bcl-2 family member, bfl-1, in B-CLL cells with an apoptosis-resistant phenotype. In this study, bfl-1 mRNA levels have been determined by competitive PCR in an extended population of B-CLL patients to characterise its role in disease progression and development of chemoresistance. bfl-1 levels were significantly higher in patients with no response (NR) to last chemotherapy than in patients responding (partial response (PR)) to last chemotherapy (P<0.05) and in patients who had not required treatment (P<0.05). We found no correlation between bfl-1 mRNA levels and disease progression, IGHV mutational status or other clinical parameters. In addition, bfl-1 mRNA levels were inversely correlated with apoptotic response to in vitro fludarabine treatment of B-CLL cells. Specific downregulation of bfl-1 using siRNA induced apoptosis in resistant cells. Our data suggest that bfl-1 contributes to chemoresistance and might be a therapeutic target in B-CLL.

Keyword

Apoptosis
B-CLL
Bfl-1
Chemoresistance
MEDICINE
MEDICIN

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