26 37

Cited 0 times in

Endogenous DEL-1 restrains melanoma lung metastasis by limiting myeloid cell-associated lung inflammation

Authors
 Young-Min Hyun  ;  Sang-Uk Seo  ;  Woo Seon Choi  ;  Hyung-Joon Kwon  ;  Dong-Young Kim  ;  Soi Jeong  ;  Gyeong-Yi Kang  ;  Eunbi Yi  ;  Minjung Kim  ;  Hyun Jin Ryu  ;  Mark R Looney  ;  Eun Young Choi  ;  Hun Sik Kim 
Citation
 SCIENCE ADVANCES, Vol.6(45) : eabc4882, 2020-11 
Journal Title
 SCIENCE ADVANCES 
Issue Date
2020-11
Abstract
Distant metastasis represents the primary cause of cancer-associated death. Pulmonary metastasis is most frequently seen in many cancers, largely driven by lung inflammation. Components from primary tumor or recruited leukocytes are known to facilitate metastasis formation. However, contribution of target site-specific host factor to metastasis is poorly understood. Here, we show that developmental endothelial locus-1 (DEL-1), an anti-inflammatory factor abundant in the lung and down-regulated by inflammatory insults, protects from melanoma lung metastasis independently of primary tumor development and systemic immunosurveillance. DEL-1 deficiency is associated with gene profiles that favor metastatic progression with inflammation and defective immunosurveillance. Mechanistically, DEL-1 deficiency primarily influences Ly6G+ neutrophil accumulation in lung metastatic niche, leading to IL-17A up-regulation from γδ T cells and reduced antimetastatic NK cells. In support, neutrophil depletion or recombinant DEL-1 treatment profoundly reverses these effects. Thus, our results identify DEL-1 as a previously unrecognized link between tumor-induced inflammation and pulmonary metastasis.
Files in This Item:
T202004660.pdf Download
DOI
10.1126/sciadv.abc4882
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Anatomy (해부학교실) > 1. Journal Papers
Yonsei Authors
Hyun, Young-Min(현영민) ORCID logo https://orcid.org/0000-0002-0567-2039
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/180371
사서에게 알리기
  feedback

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse

Links