PUBLICATION

Sarcoma cells secrete hypoxia-modified collagen VI to weaken the lung endothelial barrier and promote metastasis

Authors
Liu, Y., Murazzi, I., Fuller, A.M., Pan, H., Irizarry-Negron, V.M., DeVine, A., Katti, R., Skuli, N., Ciotti, G.E., Pak, K., Pack, M.A., Simon, M.C., Weber, K., Cooper, K., Eisinger-Mathason, T.S.K.
ID
ZDB-PUB-240210-4
Date
2024
Source
Cancer research   84(7): 977-993 (Journal)
Registered Authors
Pack, Michael
Keywords
none
MeSH Terms
  • Actins
  • Animals
  • Collagen Type VI/genetics
  • Collagen Type VI/metabolism
  • Endothelial Cells/metabolism
  • Humans
  • Hypoxia
  • Integrin beta1
  • Lung/pathology
  • Lung Neoplasms*
  • Mice
  • Sarcoma*/metabolism
  • Zebrafish/metabolism
PubMed
38335278 Full text @ Cancer Res.
Abstract
Intratumoral hypoxia correlates with metastasis and poor survival in sarcoma patients. Using an impedance sensing assay and a zebrafish intravital microinjection model, we demonstrated here that the hypoxia-inducible collagen-modifying enzyme lysyl hydroxylase PLOD2 and its substrate collagen type VI (COLVI) weaken the lung endothelial barrier and promote transendothelial migration. Mechanistically, hypoxia-induced PLOD2 in sarcoma cells modified COLVI, which was then secreted into the vasculature. Upon reaching the apical surface of lung endothelial cells, modified COLVI from tumor cells activated integrin β1 (ITGβ1). Furthermore, activated ITGβ1 co-localized with Kindlin2, initiating their interaction with F-actin and prompting its polymerization. Polymerized F-actin disrupted endothelial adherens junctions (AJ) and induced barrier dysfunction. Consistently, modified and secreted COLVI was required for the late stages of lung metastasis in vivo. Analysis of patient gene expression and survival data from The Cancer Genome Atlas (TCGA) revealed an association between the expression of both PLOD2 and COLVI and patient survival. Furthermore, high levels of COLVI were detected in surgically resected sarcoma metastases from patient lungs and in the blood of tumor-bearing mice. Together, this data identifies a mechanism of sarcoma lung metastasis, revealing opportunities for therapeutic intervention.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping