Cancer Research · 2016 · 80 citations · 45 references
MedicineCancer BiologyOncologyCancer ImmunologyMolecular OncologyTumor ProgressionChemokine NetworksCytokine BiologyLymphoid NeoplasmsLymphoid TumorsNeutrophil BiologyTumor ImmunopathologyChemokine RecruitmentChemokine-mediated Cell RecruitmentChemokine-mediated InfiltrationChemokine-mediated Leukocyte RecruitmentLymphoid Neoplasm PathogenesisLymphoma PathogenesisMalignant ProgressionTumor-associated Neutrophils
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.
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