Author:
Su Xin,Brassard Ariane,Bartolomucci Alexandra,Dhoparee-Doomah Iqraa,Qiu Qian,Tsering Thupten,Rohanizadeh Ramin,Koufos Olivia,Giannias Betty,Bourdeau France,Feng Lixuan,Leo Sabrina,Sangwan Veena,Tankel James,Quail Daniela,Spicer Jonathan,Burnier Julia V,Bailey Swneke Donovan,Ferri Lorenzo,Cools-Lartigue Jonathan
Abstract
AbstractLymph nodes (LNs) are frequently the first sites of metastasis. Currently, the only prognostic LN assessment is determining metastasis status. However, there is evidence suggesting that LN metastasis is facilitated by a pre-metastatic niche induced by tumour derived extracellular vehicles (EVs). Therefore, it is important to detect and modify the LN environmental changes. We have previously reported that neutrophil extracellular traps (NETs) can sequester and promote distant metastasis. Here, we first confirmed that LN NETs are associated with reduced patient survival. Next, we demonstrated that NETs deposition precedes LN metastasis and NETs inhibition abolishes LN metastases in animal mode. Furthermore, we discovered that EVs are essential to the formation of LN NETs. Lymphatic endothelial cells secrete CXCL8/2 in response to EVs inducing NETs formation and the promotion of LN metastasis. Our findings are the first to reveal the role of EV induced NETs in LN metastasis and provide potential immunotherapeutic vulnerabilities.Graphic AbstractIllustrative demonstration of the LNs premetastatic niche formation induced by EVs and NETs. Primary tumour constantly secretes EVs, which were actively uptaken by LECs. LECs subsequently secretes CXCL8 or CXCL2 upon EV reception. CXCL8 and CXCL2 are both neutrophil chemoattractants and potent NETs inducers. The following neutrophil recruitment and NETs formation lead to increased LN metastasis burden.
Publisher
Cold Spring Harbor Laboratory