1. Sex chromosome loss may represent a disease-associated clonal population in chronic lymphocytic leukemia
- Author
-
Iléana Antony-Debré, Hong-Anh Cung, Sylvain Choquet, Nathalie Marchay, Frederic Davi, Aurore Grelier, Karim Maloum, Laurent Sutton, Madalina Uzunov, Véronique Leblond, Elise Chapiro, Christophe Parizot, Florence Nguyen-Khac, Claude Lesty, Stéphanie Mathis, Hélène Merle-Béral, and Zahia Azgui
- Subjects
Cancer Research ,medicine.diagnostic_test ,Chronic lymphocytic leukemia ,Clone (cell biology) ,Ficoll ,Aneuploidy ,Biology ,medicine.disease ,Peripheral blood mononuclear cell ,Molecular biology ,Flow cytometry ,Leukemia ,immune system diseases ,hemic and lymphatic diseases ,Immunology ,Genetics ,medicine ,Fluorescence in situ hybridization - Abstract
Whether sex chromosome loss (SCL) is an age-related phenomenon or a cytogenetic marker of hematological disease is unclear. To address this issue in chronic lymphocytic leukemia (CLL), we investigated 20 cases with X or Y chromosome loss detected by conventional cytogenetics (CC). The frequency of SCL was low in CLL (2.3%). It was the sole abnormality, as detected by CC, in 10/20 (50%) patients. Fluorescence in situ hybridization (FISH) analyses confirmed SCL in all patients tested, present in 5-88% of cells (median: 68%). Deletions of 13q were observed by FISH in 16/20 (80%) patients. Compared with CLL without SCL, SCL was significantly associated with 13q deletion, especially when bi-allelic (P = 0.04). Co-hybridization analyses showed that SCL could be a concomitant, primary or secondary change, or be present in an independent clone. FISH analyses were performed on blood sub-populations isolated by Ficoll or flow cytometry. Comparing mononuclear cells (including CLL cells) and polynuclear cells separated by Ficoll, a maximum of 2% of polynuclear cells were found with SCL, whereas mononuclear cells exhibited a significantly higher loss frequency (range: 6-87%) (P = 0.03). Comparing B-cells (including CLL cells) and T-cells sorted by flow cytometry, the proportion of B-CD19+ cells with SCL was significantly higher (range: 88-96%) than that observed in T-CD3+ cells (range: 2-6%) (P = 0.008). We conclude that SCL has to be considered as a clonal aberration in CLL that may participate in the oncogenic process.
- Published
- 2013