Literature DB >> 19474511

Oncogene associated cDNA microarray analysis shows PRAME gene expression is a marker for response to anthracycline containing chemotherapy in patients with diffuse large B-cell lymphoma.

Riko Kawano1, Kennosuke Karube, Masahiro Kikuchi, Morishige Takeshita, Kazuo Tamura, Naokuni Uike, Tetsuya Eto, Koichi Ohshima, Junji Suzumiya.   

Abstract

CHOP (cyclophosphamide, adriamycin, vincristine, and prednisolone) therapy achieves a response in more than 60% patients with diffuse large B-cell lymphomas (DLBCLs). However, DLBCL shows a heterogeneous response to chemotherapy, and some patients are refractory to CHOP therapy. This difference in response to therapy is most likely due to differences in biological characteristics. We used cDNA microarray analysis to identify genes differentially expressed in anthracycline containing chemotherapy-resistant DLBCLs (7 patients) compared with anthracycline containing chemotherapy-sensitive DLBCLs (6 patients). Nine genes on the cDNA chip showed increased expression in anthracycline containing chemotherapy-resistant patients. We chose the preferentially expressed antigen of melanoma (PRAME) gene because it showed the highest expression in anthracycline containing chemotherapy-resistant DLBCLs on the cDNA chip, and it has been linked to prognosis of hematological malignancies. We also examined the relationship between PRAME gene expression and progression-free survival (PFS) in 45 patients with DLBCL. The progression-free survival of PRAME-positive patients (n=12) was significantly worse than that of PRAME-negative patients (n=33) (p=0.0373). Our results therefore indicate that PRAME expression in DLBCL correlates with response to anthracycline containing chemotherapy.

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Year:  2009        PMID: 19474511     DOI: 10.3960/jslrt.49.1

Source DB:  PubMed          Journal:  J Clin Exp Hematop        ISSN: 1346-4280


  5 in total

1.  A panel of cancer-testis genes exhibiting broad-spectrum expression in haematological malignancies.

Authors:  Amanda P Liggins; Seah H Lim; Elizabeth J Soilleux; Karen Pulford; Alison H Banham
Journal:  Cancer Immun       Date:  2010-08-23

Review 2.  Leucine-rich repeat protein PRAME: expression, potential functions and clinical implications for leukaemia.

Authors:  Frances Wadelin; Joel Fulton; Paul A McEwan; Keith A Spriggs; Jonas Emsley; David M Heery
Journal:  Mol Cancer       Date:  2010-08-27       Impact factor: 27.401

3.  Prognostic significance of PRAME expression based on immunohistochemistry for diffuse large B-cell lymphoma patients treated with R-CHOP therapy.

Authors:  Kenjiro Mitsuhashi; Akihiro Masuda; Yan-Hua Wang; Masayuki Shiseki; Toshiko Motoji
Journal:  Int J Hematol       Date:  2014-05-13       Impact factor: 2.490

4.  The expansion of the PRAME gene family in Eutheria.

Authors:  Ti-Cheng Chang; Yang Yang; Hiroshi Yasue; Arvind K Bharti; Ernest F Retzel; Wan-Sheng Liu
Journal:  PLoS One       Date:  2011-02-10       Impact factor: 3.240

5.  Knock-down of PRAME increases retinoic acid signaling and cytotoxic drug sensitivity of Hodgkin lymphoma cells.

Authors:  Stefanie Kewitz; Martin S Staege
Journal:  PLoS One       Date:  2013-02-11       Impact factor: 3.240

  5 in total

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