Subnetwork-based analysis of chronic lymphocytic leukemia identifies pathways that associate with disease progression

被引:59
作者
Chuang, Han-Yu [2 ,3 ,4 ]
Rassenti, Laura [3 ,4 ]
Salcedo, Michelle [5 ]
Licon, Kate [2 ,3 ]
Kohlmann, Alexander [6 ]
Haferlach, Torsten [7 ]
Foa, Robin [8 ]
Ideker, Trey [1 ,2 ,3 ,4 ]
Kipps, Thomas J. [3 ,4 ]
机构
[1] Univ Calif San Diego, SKAGGS, Bioinformat & Syst Biol Program, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[6] Roche Mol Syst Inc, Dept Genom & Oncol, Pleasanton, CA USA
[7] MLL Munchner Leukamielabor GmbH, Munich, Germany
[8] Univ Roma La Sapienza, Div Hematol, Rome, Italy
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
INTERACTION NETWORK DATABASE; PROTEIN INTERACTION NETWORK; GENE-EXPRESSION PROFILE; GROWTH-FACTOR-BETA; B-CELLS; MUTATION STATUS; BREAST-CANCER; CLASSIFICATION; ACTIVATION; REPOSITORY;
D O I
10.1182/blood-2012-03-416461
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical course of patients with chronic lymphocytic leukemia (CLL) is heterogeneous. Several prognostic factors have been identified that can stratify patients into groups that differ in their relative tendency for disease progression and/or survival. Here, we pursued a subnetwork-based analysis of gene expression profiles to discriminate between groups of patients with disparate risks for CLL progression. From an initial cohort of 130 patients, we identified 38 prognostic subnetworks that could predict the relative risk for disease progression requiring therapy from the time of sample collection, more accurately than established markers. The prognostic power of these subnetworks then was validated on 2 other cohorts of patients. We noted reduced divergence in gene expression between leukemia cells of CLL patients classified at diagnosis with aggressive versus indolent disease over time. The predictive subnetworks vary in levels of expression over time but exhibit increased similarity at later time points before therapy, suggesting that degenerate pathways apparently converge into common pathways that are associated with disease progression. As such, these results have implications for understanding cancer evolution and for the development of novel treatment strategies for patients with CLL. (Blood. 2012; 120(13):2639-2649)
引用
收藏
页码:2639 / 2649
页数:11
相关论文
共 52 条
  • [1] The Biomolecular Interaction Network Database and related tools 2005 update
    Alfarano, C
    Andrade, CE
    Anthony, K
    Bahroos, N
    Bajec, M
    Bantoft, K
    Betel, D
    Bobechko, B
    Boutilier, K
    Burgess, E
    Buzadzija, K
    Cavero, R
    D'Abreo, C
    Donaldson, I
    Dorairajoo, D
    Dumontier, MJ
    Dumontier, MR
    Earles, V
    Farrall, R
    Feldman, H
    Garderman, E
    Gong, Y
    Gonzaga, R
    Grytsan, V
    Gryz, E
    Gu, V
    Haldorsen, E
    Halupa, A
    Haw, R
    Hrvojic, A
    Hurrell, L
    Isserlin, R
    Jack, F
    Juma, F
    Khan, A
    Kon, T
    Konopinsky, S
    Le, V
    Lee, E
    Ling, S
    Magidin, M
    Moniakis, J
    Montojo, J
    Moore, S
    Muskat, B
    Ng, I
    Paraiso, JP
    Parker, B
    Pintilie, G
    Pirone, R
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 : D418 - D424
  • [2] Computational analysis of the synergy among multiple interacting genes
    Anastassiou, Dimitris
    [J]. MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
  • [3] BIND - The Biomolecular Interaction Network Database
    Bader, GD
    Donaldson, I
    Wolting, C
    Ouellette, BFF
    Pawson, T
    Hogue, CWV
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (01) : 242 - 245
  • [4] TGF-β and cancer
    Bierie, B
    Moses, HL
    [J]. CYTOKINE & GROWTH FACTOR REVIEWS, 2006, 17 (1-2) : 29 - 40
  • [5] A network-based analysis of systemic inflammation in humans
    Calvano, SE
    Xiao, WZ
    Richards, DR
    Felciano, RM
    Baker, HV
    Cho, RJ
    Chen, RO
    Brownstein, BH
    Cobb, JP
    Tschoeke, SK
    Miller-Graziano, C
    Moldawer, LL
    Mindrinos, MN
    Davis, RW
    Tompkins, RG
    Lowry, SF
    [J]. NATURE, 2005, 437 (7061) : 1032 - 1037
  • [6] Network-based classification of breast cancer metastasis
    Chuang, Han-Yu
    Lee, Eunjung
    Liu, Yu-Tsueng
    Lee, Doheon
    Ideker, Trey
    [J]. MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
  • [7] Ig V gene mutation status and CD38 expression as novel prognostic indicators in chronic lymphocytic leukemia
    Damle, RN
    Wasil, T
    Fais, F
    Ghiotto, F
    Valetto, A
    Allen, SL
    Buchbinder, A
    Budman, D
    Dittmar, K
    Kolitz, J
    Lichtman, SM
    Schulman, P
    Vinciguerra, VP
    Rai, KR
    Ferrarini, M
    Chiorazzi, N
    [J]. BLOOD, 1999, 94 (06) : 1840 - 1847
  • [8] Molecular pathogenesis of chronic lymphocytic leukemia
    Danilov, Alexey V.
    Danilova, Olga V.
    Klein, Andreas K.
    Huber, Brigitte T.
    [J]. CURRENT MOLECULAR MEDICINE, 2006, 6 (06) : 665 - 675
  • [9] MAPPFinder: using Gene Ontology and GenMAPP to create a global gene-expression profile from microarray data
    Doniger, SW
    Salomonis, N
    Dahlquist, KD
    Vranizan, K
    Lawlor, SC
    Conklin, BR
    [J]. GENOME BIOLOGY, 2003, 4 (01)
  • [10] Chronic lymphocytic leukemia B cells are resistant to the apoptotic effects of transforming growth factor-beta
    Douglas, RS
    Capocasale, RJ
    Lamb, RJ
    Nowell, PC
    Moore, JS
    [J]. BLOOD, 1997, 89 (03) : 941 - 947