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PMID: 23144194 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Association between B-cell receptor responsiveness and disease progression in B-cell chronic lymphocytic leukemia: results from single cell network profiling studies.

Haematologica ·Vol. 98 ·No. 4 ·2013-04-00 ·页码 626-34

Cesano A, Perbellini O, Evensen E, Chu CC, Cioffi F, Ptacek J, Damle RN, Chignola R, Cordeiro J, Yan XJ, Hawtin RE, Nichele I, Ware JR, Cavallini C, Lovato O, Zanotti R, Rai KR, Chiorazzi N, Pizzolo G, Scupoli MT

Abstract

While many prognostic markers in B-cell chronic lymphocytic leukemia provide insight into the biology of the disease, few have been demonstrated to be useful in the daily management of patients. B-cell receptor signaling is a driving event in the progression of B-cell chronic lymphocytic leukemia and markers of B-cell receptor responsiveness have been shown to be of prognostic value. Single cell network profiling, a multiparametric flow cytometry-based assay, allows functional signaling analysis at the level of the single cell. B-cell receptor signaling proteins (i.e. p-SYK, p-NF-κB p65, p-ERK, p-p38, p-JNK) were functionally characterized by single cell network profiling in samples from patients with B-cell chronic lymphocytic leukemia in an exploratory study (n=27) after stimulation with anti-IgM. Significant associations of single cell network profiling data with clinical outcome (i.e. time to first treatment), as assessed by Cox regression models, were then confirmed in patients' samples in two other sequential independent studies, i.e. test study 1 (n=30), and test study 2 (n=37). In the exploratory study, higher responsiveness of the B-cell receptor signaling proteins to anti-IgM was associated with poor clinical outcomes. Patients' clustering based on signaling response was at least as powerful in discriminating different disease courses as traditional prognostic markers. In an unselected subgroup of patients with Binet stage A disease (n=21), increased anti-IgM-modulated p-ERK signaling was shown to be a significant, independent predictor of shorter time to first treatment. This result was independently confirmed in two test cohorts from distinct populations of patients. In conclusion, these findings support the utility of the single cell network profiling assay in elucidating signaling perturbations with the potential for the development of a clinically useful prognostic test in patients with early stage B-cell chronic lymphocytic leukemia. These data support the clinical relevance of B-cell receptor signaling in B-cell chronic lymphocytic leukemia, and suggest a key role of ERK activation in the physiopathology of this leukemia.

MeSH 主题词
Adult Aged Aged, 80 and over Antibodies, Anti-Idiotypic/pharmacology Cells, Cultured Disease Progression Extracellular Signal-Regulated MAP Kinases/metabolism Female Flow Cytometry/methods,statistics & numerical data Humans Intracellular Signaling Peptides and Proteins/metabolism Kaplan-Meier Estimate Leukemia, Lymphocytic, Chronic, B-Cell/blood,metabolism,pathology Leukocytes, Mononuclear/drug effects,metabolism Male Middle Aged Multivariate Analysis NF-kappa B/metabolism Prognosis Proportional Hazards Models Protein-Tyrosine Kinases/metabolism Receptors, Antigen, B-Cell/metabolism Signal Transduction/drug effects Single-Cell Analysis/methods Syk Kinase
化学物质
Antibodies, Anti-Idiotypic Intracellular Signaling Peptides and Proteins NF-kappa B Receptors, Antigen, B-Cell anti-IgM Protein-Tyrosine Kinases SYK protein, human Syk Kinase Extracellular Signal-Regulated MAP Kinases
作者与单位
共 20 位作者,点击展开单位 / ORCID
Cesano Alessandra
Nodality Inc., South San Francisco, CA, USA.
Perbellini Omar
Evensen Erik
Chu Charles C
Cioffi Federica
Ptacek Jason
Damle Rajendra N
Chignola Roberto
Cordeiro James
Yan Xiao-jie
Hawtin Rachael E
Nichele Ilaria
Ware Jodi R
Cavallini Chiara
Lovato Ornella
Zanotti Roberta
Rai Kanti R
Chiorazzi Nicholas
Pizzolo Giovanni
Scupoli Maria T
Article Info
Journal
Haematologica
Abbr.
Haematologica
ISSN
1592-8721
Published
2013-04-00
电子出版
2012-00-09
页码
626-34
Language
English
Country/Region
Italy
NLM ID
0417435
基金资助
NCI NIH HHS · R01 CA081554 · United States
NCI NIH HHS · R01 CA81554 · United States
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