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Macrophage ABHD5 Suppresses NFκB-Dependent Matrix Metalloproteinase Expression and Cancer Metastasis.

Authors :
Shang S
Ji X
Zhang L
Chen J
Li C
Shi R
Xiang W
Kang X
Zhang D
Yang F
Dai R
Chen P
Chen S
Chen Y
Li Y
Miao H
Source :
Cancer research [Cancer Res] 2019 Nov 01; Vol. 79 (21), pp. 5513-5526. Date of Electronic Publication: 2019 Aug 22.
Publication Year :
2019

Abstract

Metabolic reprogramming in tumor-associated macrophages (TAM) is associated with cancer development, however, the role of macrophage triglyceride metabolism in cancer metastasis is unclear. Here, we showed that TAMs exhibited heterogeneous expression of abhydrolase domain containing 5 (ABHD5), an activator of triglyceride hydrolysis, with migratory TAMs expressing lower levels of ABHD5 compared with the nonmigratory TAMs. ABHD5 expression in macrophages inhibited cancer cell migration in vitro in xenograft models and in genetic cancer models. The effects of macrophage ABHD5 on cancer cell migration were dissociated from its metabolic function as neither triglycerides nor ABHD5-regulated metabolites from macrophages affected cancer cell migration. Instead, ABHD5 deficiency in migrating macrophages promoted NFκB p65-dependent production of matrix metalloproteinases (MMP). ABHD5 expression negatively correlated with MMP expression in TAMs and was associated with better survival in patients with colorectal cancer. Taken together, our findings show that macrophage ABHD5 suppresses NFκB-dependent MMP production and cancer metastasis and may serve as a prognostic marker in colorectal cancer. SIGNIFICANCE: These findings highlight the mechanism by which reduced expression of the metabolic enzyme ABHD5 in macrophages promotes cancer metastasis. Graphical Abstract: http://cancerres.aacrjournals.org/content/canres/79/21/5513/F1.large.jpg.<br /> (©2019 American Association for Cancer Research.)

Details

Language :
English
ISSN :
1538-7445
Volume :
79
Issue :
21
Database :
MEDLINE
Journal :
Cancer research
Publication Type :
Academic Journal
Accession number :
31439546
Full Text :
https://doi.org/10.1158/0008-5472.CAN-19-1059