| Literature DB >> 27923834 |
Benoit Manfroi1, Thomas McKee2, Jean Francois Mayol3, Sebastien Tabruyn3, Sebastien Moret4, Christian Villiers1, Christian Righini5, Martin Dyer6, Mary Callanan1, Pascal Schneider7, Alexandar Tzankov8, Thomas Matthes9, Nathalie Sturm1,10, Bertrand Huard11.
Abstract
Tumor-infiltrating neutrophils have been implicated in malignant development and progression, but mechanisms are ill defined. Neutrophils produce a proliferation-inducing ligand APRIL/TNFSF13, a factor that promotes development of tumors from diverse origins, including diffuse large B-cell lymphoma (DLBCL). High APRIL expression in DLBCL correlates with reduced patient survival, but the pathway(s) dictating APRIL expression are not known. Here, we show that all blood neutrophils constitutively secrete APRIL, and inflammation-associated stimuli, such as TNF, further upregulate APRIL. In a significant fraction of DLBCL patients, tumor cells constitutively produced the ELC-CXC chemokine CXCL-8 (IL8), enabling them to recruit APRIL-producing blood neutrophils. CXCL-8 production in DLBCL was unrelated to the cell of origin, as APRIL-producing neutrophils infiltrated CXCL-8+ DLBCL from both germinal center (GC) and non-GC subtypes. Rather, CXCL-8 production implied events affecting DNA methylation and acetylation. Overall, our results showed that chemokine-mediated recruitment of neutrophils secreting the tumor-promoting factor APRIL mediates DLBCL progression. Cancer Res; 77(5); 1097-107. ©2016 AACR. ©2016 American Association for Cancer Research.Entities:
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Year: 2016 PMID: 27923834 DOI: 10.1158/0008-5472.CAN-16-0786
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701