Melanoma-derived small extracellular vesicles induce lymphangiogenesis and metastasis through an NGFR-dependent mechanism Journal Article


Authors: García-Silva, S.; Benito-Martín, A.; Nogués, L.; Hernández-Barranco, A.; Mazariegos, M. S.; Santos, V.; Hergueta-Redondo, M.; Ximénez-Embún, P.; Kataru, R. P.; Lopez, A. A.; Merino, C.; Sánchez-Redondo, S.; Graña-Castro, O.; Matei, I.; Nicolás-Avila, J. Á; Torres-Ruiz, R.; Rodríguez-Perales, S.; Martínez, L.; Pérez-Martínez, M.; Mata, G.; Szumera-Ciećkiewicz, A.; Kalinowska, I.; Saltari, A.; Martínez-Gómez, J. M.; Hogan, S. A.; Saragovi, H. U.; Ortega, S.; Garcia-Martin, C.; Boskovic, J.; Levesque, M. P.; Rutkowski, P.; Hidalgo, A.; Muñoz, J.; Megías, D.; Mehrara, B. J.; Lyden, D.; Peinado, H.
Article Title: Melanoma-derived small extracellular vesicles induce lymphangiogenesis and metastasis through an NGFR-dependent mechanism
Abstract: Secreted extracellular vesicles (EVs) influence the tumor microenvironment and promote distal metastasis. Here we analyzed the involvement of melanoma-secreted EVs in lymph node pre-metastatic niche formation in murine models. We found that small EVs (sEVs) derived from metastatic melanoma cell lines were enriched in nerve growth factor (NGF) receptor (NGFR, p75NTR), spread through the lymphatic system and were taken up by lymphatic endothelial cells, reinforcing lymph node metastasis. Remarkably, sEVs enhanced lymphangiogenesis and tumor cell adhesion by inducing ERK kinase, nuclear factor (NF)-κB activation and intracellular adhesion molecule (ICAM)-1 expression in lymphatic endothelial cells. Importantly, ablation or inhibition of NGFR in sEVs reversed the lymphangiogenic phenotype, decreased lymph node metastasis and extended survival in pre-clinical models. Furthermore, NGFR expression was augmented in human lymph node metastases relative to that in matched primary tumors, and the frequency of NGFR+ metastatic melanoma cells in lymph nodes correlated with patient survival. In summary, we found that NGFR is secreted in melanoma-derived sEVs, reinforcing lymph node pre-metastatic niche formation and metastasis. © 2021, The Author(s), under exclusive licence to Springer Nature America, Inc.
Keywords: immunohistochemistry; cancer survival; controlled study; protein expression; human cell; sequence analysis; nonhuman; flow cytometry; lymph node metastasis; mouse; electron microscopy; animal tissue; melanoma; metastasis; gene expression; confocal microscopy; image analysis; animal experiment; animal model; cohort analysis; immunoglobulin enhancer binding protein; immunofluorescence; in vitro study; enzyme activity; biopsy; histology; endothelium cell; lymphangiogenesis; immune response; pilot study; western blotting; immunoblotting; mitogen activated protein kinase 1; mitogen activated protein kinase 3; down regulation; eosin; hematoxylin; upregulation; centrifugation; cell adhesion; short hairpin rna; bioluminescence; intercellular adhesion molecule 1; rna extraction; polyacrylamide gel electrophoresis; rna sequence; tumor microenvironment; colony formation; nerve growth factor receptor; housekeeping gene; exosome; neurotrophin receptor; preclinical study; human; male; article; clustered regularly interspaced short palindromic repeat; 4',6 diamidino 2 phenylindole; melanoma cell line; mrna expression level
Journal Title: Nature Cancer
Volume: 2
Issue: 12
ISSN: 2662-1347
Publisher: Nature Research  
Date Published: 2021-12-01
Start Page: 1387
End Page: 1405
Language: English
DOI: 10.1038/s43018-021-00272-y
PROVIDER: scopus
PMCID: PMC8697753
PUBMED: 34957415
DOI/URL:
Notes: Article -- Export Date: 1 February 2022 -- Source: Scopus
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  1. Babak Mehrara
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  2. Raghu Prasad Kataru
    61 Kataru