A comparison of the effects of romidepsin treatment on gene expression in a leukemic patient with sezary syndrome using two different methods for blood collection

2021 ◽  
Author(s):  
Shere Shievonne Billouin
Cells ◽  
2020 ◽  
Vol 9 (9) ◽  
pp. 1992
Author(s):  
Andrea Moerman-Herzog ◽  
Syed J. Mehdi ◽  
Henry K. Wong

Sézary syndrome (SS), an aggressive cutaneous T-cell lymphoma (CTCL) with poor prognosis, is characterized by the clinical hallmarks of circulating malignant T cells, erythroderma and lymphadenopathy. However, highly variable clinical skin manifestations and similarities with benign mimickers can lead to significant diagnostic delay and inappropriate therapy that can lead to disease progression and mortality. SS has been the focus of numerous transcriptomic-profiling studies to identify sensitive and specific diagnostic and prognostic biomarkers. Benign inflammatory disease controls (e.g., psoriasis, atopic dermatitis) have served to identify chronic inflammatory phenotypes in gene expression profiles, but provide limited insight into the lymphoproliferative and oncogenic roles of abnormal gene expression in SS. This perspective was recently clarified by a transcriptome meta-analysis comparing SS and lymphocytic-variant hypereosinophilic syndrome, a benign yet often clonal T-cell lymphoproliferation, with clinical features similar to SS. Here we review the rationale for selecting lymphocytic-variant hypereosinophilic syndrome (L-HES) as a disease control for SS, and discuss differentially expressed genes that may distinguish benign from malignant lymphoproliferative phenotypes, including additional context from prior gene expression studies to improve understanding of genes important in SS.


2004 ◽  
Vol 64 (16) ◽  
pp. 5578-5586 ◽  
Author(s):  
Remco van Doorn ◽  
Remco Dijkman ◽  
Maarten H. Vermeer ◽  
Jacoba J. Out-Luiting ◽  
Elisabeth M. H. van der Raaij-Helmer ◽  
...  

2010 ◽  
Vol 130 (4) ◽  
pp. 1116-1125 ◽  
Author(s):  
Christine L. Jones ◽  
E. Mary Wain ◽  
Chung-Ching Chu ◽  
Isabella Tosi ◽  
Rosalind Foster ◽  
...  

Oncotarget ◽  
2017 ◽  
Vol 8 (24) ◽  
pp. 39627-39639 ◽  
Author(s):  
Katarzyna Iżykowska ◽  
Grzegorz K. Przybylski ◽  
Claudia Gand ◽  
Floriane C. Braun ◽  
Piotr Grabarczyk ◽  
...  

Blood ◽  
2009 ◽  
Vol 113 (1) ◽  
pp. 127-136 ◽  
Author(s):  
Remco van Doorn ◽  
Marloes S. van Kester ◽  
Remco Dijkman ◽  
Maarten H. Vermeer ◽  
Aat A. Mulder ◽  
...  

Abstract Mycosis fungoides (MF), the most common cutaneous T-cell lymphoma, is a malignancy of mature, skin-homing T cells. Sézary syndrome (Sz) is often considered to represent a leukemic phase of MF. In this study, the pattern of numerical chromosomal alterations in MF tumor samples was defined using array-based comparative genomic hybridization (CGH); simultaneously, gene expression was analyzed using microarrays. Highly recurrent chromosomal alterations in MF include gain of 7q36, 7q21-7q22 and loss of 5q13 and 9p21. The pattern characteristic of MF differs markedly from chromosomal alterations observed in Sz. Integration of data from array-based CGH and gene-expression analysis yielded several candidate genes with potential relevance in the pathogenesis of MF. We confirmed that the FASTK and SKAP1 genes, residing in loci with recurrent gain, demonstrated increased expression. The RB1 and DLEU1 tumor suppressor genes showed diminished expression associated with loss. In addition, it was found that the presence of chromosomal alterations on 9p21, 8q24, and 1q21-1q22 was associated with poor prognosis in patients with MF. This study provides novel insight into genetic alterations underlying MF. Furthermore, our analysis uncovered genomic differences between MF and Sz, which suggest that the molecular pathogenesis and therefore therapeutic requirements of these cutaneous T-cell lymphomas may be distinct.


2010 ◽  
Vol 163 (5) ◽  
pp. 1090-1094 ◽  
Author(s):  
R.G. Pomerantz ◽  
E.D. Mirvish ◽  
G. Erdos ◽  
L.D. Falo ◽  
L.J. Geskin

Blood ◽  
2013 ◽  
Vol 121 (8) ◽  
pp. 1477-1478 ◽  
Author(s):  
L. Michel ◽  
F. Jean-Louis ◽  
E. Begue ◽  
A. Bensussan ◽  
M. Bagot

1970 ◽  
Vol 101 (2) ◽  
pp. 244-246 ◽  
Author(s):  
H. H. Roenigk

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