Role of Interleukin 16 in Multiple Myeloma

被引:45
作者
Atanackovic, Djordje [1 ]
Hildebrandt, York [2 ]
Templin, Julia [1 ]
Cao, Yanran [1 ]
Keller, Christiane [1 ]
Panse, Jens [1 ]
Meyer, Sabrina [1 ]
Reinhard, Henrike [1 ]
Bartels, Katrin [1 ]
Lajmi, Nesrine [1 ]
Sezer, Orhan [1 ]
Zander, Axel R. [2 ]
Marx, Andreas H. [3 ]
Uhlig, Ria [3 ]
Zustin, Jozef [3 ]
Bokemeyer, Carsten [1 ]
Kroeger, Nicolaus [2 ]
机构
[1] Hubertus Wald Tumorzentrum, Univ Canc Ctr Hamburg, Dept Internal Med 2, Ctr Oncol, Hamburg, Germany
[2] Univ Med Ctr Hamburg Eppendorf, Dept Stem Cell Transplantat, D-20246 Hamburg, Germany
[3] Univ Med Ctr Hamburg Eppendorf, Inst Pathol, D-20246 Hamburg, Germany
关键词
LYMPHOCYTE CHEMOATTRACTANT FACTOR; STIMULATING FACTOR-RECEPTOR; T-CELL-ACTIVATION; MEMORY B-CELLS; HUMAN EOSINOPHILS; SERUM-LEVELS; MAST-CELLS; TETRASPANIN CD9; DENDRITIC CELLS; IL-16;
D O I
10.1093/jnci/djs257
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Multiple myeloma is a malignancy characterized by the expansion of a plasma cell clone that localizes to the human bone marrow. Myeloma cells and bone marrow stromal cells produce soluble factors that promote the survival and progression of multiple myeloma. Interleukin 16 (IL-16) is involved in regulating the migration and proliferation of normal leukocytes. However, the role of IL-16 in human cancers, including multiple myeloma, is unclear. Methods We investigated IL-16 expression in cell lines (n = 10) and in the bone marrow of myeloma patients (n = 62) and healthy bone marrow donors (n = 12) by quantitative reverse transcription-polymerase chain reaction, immunoblot analysis, enzyme-linked immunosorbent assay, flow cytometry, and immunohistochemistry. Transfection of two human multiple myeloma cell lines with small interfering RNAs was used to examine the effect of IL-16 gene silencing on apoptosis by flow cytometry, on proliferation by bromodeoxyuridine incorporation, and on colony formation. Protein neutralization assays were performed by treating multiple myeloma cells with a monoclonal antibody against the carboxyl-terminal fragment of IL-16. All statistical tests were two-sided. Results IL-16 was strongly overexpressed in the bone marrow of myeloma patients compared with healthy donors. Myeloma cell lines as well as primary tumor cells from myeloma patients constitutively expressed IL-16 and its receptors CD4 and/or CD9 and spontaneously secreted soluble IL-16. Silencing of IL-16 reduced the proliferative activity of myeloma cells by approximately 80% compared with untreated cells (mean relative proliferative activity IL-16 siRNA vs untransfected cells, EJM cells: 20.1%, 95% confidence interval [CI] = 14.3% to 26.0%, P = .03; KMS-12-BM cells: 22.8%, 95% CI = 5.5% to 40.0%, P = .04), and addition of a recombinant carboxyl-terminal IL-16 peptide reversed that effect. A monoclonal antibody directed against IL-16 or its receptors had a comparably strong growth-inhibiting effect on the tumor cells. Conclusions IL-16 is an important growth-promoting factor in multiple myeloma and a candidate for novel diagnostic, prognostic, and therapeutic applications for this incurable human malignancy. J Natl Cancer Inst 2012;104:1005-1020
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收藏
页码:1005 / 1020
页数:16
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