FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2912119954> ?p ?o ?g. }

• W2912119954 endingPage "939" @default.
• W2912119954 startingPage "937" @default.
• W2912119954 abstract "See article on page 1087 Work from the author’s laboratory is supported by grants from the National Institutes of Health, Digestive Disease Research Core Center (DK‐52574 [ARAC], DK‐56260, and DK‐112378). Potential conflict of interest: Nothing to report. There is increasing interest in the role of angiogenesis in fibrogenic signaling through generation of proangiogenic mediators that perpetuate injury and promote fibrosis (reviewed in Bocca et al.1). This is a timely development in understanding the underlying mechanisms and pathways that promote progression of nonalcoholic fatty liver disease (NAFLD) to nonalcoholic steatohepatitis (NASH) with fibrosis and hepatocellular cancer (HCC), given the global impact of these diseases.2 A role for angiogenesis in the progression of human NAFLD/NASH was shown a decade ago in studies where increased cluster of differentiation 34 (CD34) immunostaining (a surrogate for neovascularization) was observed in liver samples from NASH patients and in particular those with F2‐F4 fibrosis.3 Predicated in part by those findings in humans, other studies examined the role for angiogenic signaling in preclinical models of NASH, including through vascular endothelial growth factor (VEGF) and placental growth factor (PlGF) signaling.4 Those studies demonstrated that mice fed a methionine‐choline‐deficient (MCD) diet exhibited increased angiogenesis with a significant increase in both angiogenic and inflammatory mediators.4 Treatment of MCD diet–fed mice with anti–VEGF receptor 2 antibody decreased the angiogenic response, reduced vascular architectural distortion, and attenuated both inflammation and steatosis, while anti‐PlGF antibody treatment of MCD diet–fed mice was ineffective at mitigating those adverse events.4 So, at least in mice fed an MCD diet, the findings suggest that hepatic steatosis and inflammation are associated with an abnormal angiogenic response that may together further promote fibrogenesis and that inhibiting VEGF signaling is potentially therapeutic. The work by Lefere and colleagues in the current issue of hepatology5 addresses those questions by studying a key signaling pathway involved in angiogenesis, namely the tyrosine kinase with immunoglobulin and epidermal growth factor homology domains 1/2 (Tie1/Tie2) receptor complex and angiopoietin (ANG) ligands. Tie receptors exist in two forms, Tie1 and Tie2, which interact and both of which are required for normal angiogenesis (reviewed in Mueller and Kontos6). Angiopoietins (principally ANG1 and ANG2) function by signaling through Tie receptors to regulate normal developmental angiogenesis and, depending on the circumstances (described below), as either context‐dependent agonists or antagonists of Tie2 signaling. This dual role is explained in part because Tie1 is considered an orphan receptor with no naturally identified ligand but rather modulates ANG signaling through Tie2.6 ANG1 signaling through Tie1/Tie2 promotes normal vascular homeostasis under basal (i.e., noninflammatory) conditions; but in the setting of inflammatory mediators the Tie1 receptor undergoes cleavage of its ectodomain, and ANG2 then becomes the dominant angiogenic signal, where it functions as a Tie2 antagonist and promotes a neoangiogenic, abnormal vasculature, prone to increased leakage.7 The inflammation‐associated cleavage of Tie1 thus initiates a feed‐forward activation loop in which ANG2 promotes abnormal vascular remodeling.8 Lefere and colleagues show that serum ANG2 levels are increased in NASH patients and in proportion to the histological grade of inflammation, steatosis, and ballooning, although surprisingly not with the degree of fibrosis.5 They further show that serum ANG2 levels correlate with CD34 immunohistochemical staining in liver sections, with reactivity confined to macrophages and endothelial cells. Those findings together strongly suggest that NASH subjects display increased circulating serum levels of ANG2, which correlates with markers of neovascularization (as indicated by CD34 staining) and that hepatic vascular endothelial cells are a plausible source of ANG2. In the next phase, the authors undertook to inhibit the antagonistic role of ANG2 signaling through Tie2, using an engineered antibody (L1‐10) that blocks ANG2–Tie2 interaction. They show that MCD diet–fed mice exhibit increased serum ANG2 levels, confirming the expected findings alluded to above. They also studied another NASH model, namely neonatal streptozotocin and 16 weeks of western diet exposure,9 and confirmed that ANG2 serum levels were increased in that model also. Administration of L1‐10 reduced inflammation, ballooning, and fibrosis in MCD diet–fed mice but did not change the degree of steatosis. The authors further undertook elegant three‐dimensional reconstruction imaging of the hepatic vasculature in those various groups of MCD diet–fed mice and demonstrated that L1‐10 treatment, as either a preventive or a therapeutic intervention, reduced abnormal angiogenesis with decreased vascular density compared to placebo.5 They also showed that L1‐10 treatment reduced angiogenic signaling from cultured endothelial cells following lipopolysaccharide stimulation, confirming their observations that L1‐10 reduces neoangiogenesis primarily through cell autonomous (i.e., endothelial) signaling. In a final series of studies, the authors returned to the streptozotocin–western diet model of NASH and asked if L1‐10 would mitigate the development of HCC. They show that steatosis and histologic inflammation were unaltered in the L1‐10‐treated group, although there was a trend to reduced fibrosis and reduced mRNA expression of proinflammatory cytokines. In addition, they observed a decreased tumor burden in the L1‐10‐treated mice with reduced expression of glypican‐3 and heat shock protein 70 as well as reduced alpha‐fetoprotein. Those findings suggest that L1‐10 treatment attenuates tumorigenesis in experimental NASH‐associated HCC, although the underlying mechanisms are still to be explored.5 These elegant and comprehensive studies provide a tantalizing insight into the complex, multicellular signaling network that modulates NAFLD → NASH → HCC progression and further raise the prospect for targeted therapeutic interventions. There are distinctive differences, however, in the pathways at play with ANG2–Tie interactions compared, say, to other angiogenic pathways that have been studied in the context of experimental NASH. Among these differences is that anti‐VEGF receptor 2 treatment in MCD diet–fed mice led to reduced hepatic steatosis,4 while L1‐10 had no effect. Presumably those antiangiogenic interventions differ in the downstream effects on hepatic lipogenesis and/or other homeostatic pathways. Another question is the role of inflammatory mediators in the initial process of cleaving the ectodomain of Tie1. What is the protease involved, and is baseline inflammation a prerequisite for L1‐10 to ameliorate further damage? Would L1‐10 treatment mitigate fibrosis in other, less inflammatory preclinical models of hepatic steatosis? Among the other intriguing findings from this study is the observation that L1‐10 reduced the tumor burden in a preclinical model of NASH‐associated HCC. Those findings are important because high circulating levels of ANG2 are a strong negative predictor of overall patient survival in HCC.10 However, in a recent study using trebenanib (which sequesters ANG1 and ANG2 and blocks interaction with Tie2) in addition to standard sorafenib treatment, there was no improvement in progression‐free survival in patients with advanced HCC.10 The studies of Lefere and colleagues will hopefully propel further investigation of this important signaling pathway, which could in turn pave the way for clinical trials." @default.
• W2912119954 created "2019-02-21" @default.
• W2912119954 creator A5023095216 @default.
• W2912119954 date "2019-02-08" @default.
• W2912119954 modified "2023-09-23" @default.
• W2912119954 title "Tie‐ing Up Angiogenesis to Treat Nonalcoholic Steatohepatitis" @default.
• W2912119954 cites W1831467892 @default.
• W2912119954 cites W1874465904 @default.
• W2912119954 cites W2025579102 @default.
• W2912119954 cites W2092873757 @default.
• W2912119954 cites W2515730584 @default.
• W2912119954 cites W2515960821 @default.
• W2912119954 cites W2517498730 @default.
• W2912119954 cites W2621795045 @default.
• W2912119954 cites W2759997926 @default.
• W2912119954 cites W2893730472 @default.
• W2912119954 doi "https://doi.org/10.1002/hep.30318" @default.
• W2912119954 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6393173" @default.
• W2912119954 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30325071" @default.
• W2912119954 hasPublicationYear "2019" @default.
• W2912119954 type Work @default.
• W2912119954 sameAs 2912119954 @default.
• W2912119954 citedByCount "1" @default.
• W2912119954 countsByYear W29121199542021 @default.
• W2912119954 crossrefType "journal-article" @default.
• W2912119954 hasAuthorship W2912119954A5023095216 @default.
• W2912119954 hasBestOaLocation W29121199542 @default.
• W2912119954 hasConcept C126322002 @default.
• W2912119954 hasConcept C2776954865 @default.
• W2912119954 hasConcept C2778772119 @default.
• W2912119954 hasConcept C2779134260 @default.
• W2912119954 hasConcept C2779478299 @default.
• W2912119954 hasConcept C2780394083 @default.
• W2912119954 hasConcept C3018708256 @default.
• W2912119954 hasConcept C71924100 @default.
• W2912119954 hasConceptScore W2912119954C126322002 @default.
• W2912119954 hasConceptScore W2912119954C2776954865 @default.
• W2912119954 hasConceptScore W2912119954C2778772119 @default.
• W2912119954 hasConceptScore W2912119954C2779134260 @default.
• W2912119954 hasConceptScore W2912119954C2779478299 @default.
• W2912119954 hasConceptScore W2912119954C2780394083 @default.
• W2912119954 hasConceptScore W2912119954C3018708256 @default.
• W2912119954 hasConceptScore W2912119954C71924100 @default.
• W2912119954 hasIssue "3" @default.
• W2912119954 hasLocation W29121199541 @default.
• W2912119954 hasLocation W29121199542 @default.
• W2912119954 hasLocation W29121199543 @default.
• W2912119954 hasLocation W29121199544 @default.
• W2912119954 hasOpenAccess W2912119954 @default.
• W2912119954 hasPrimaryLocation W29121199541 @default.
• W2912119954 hasRelatedWork W2083817683 @default.
• W2912119954 hasRelatedWork W2130310686 @default.
• W2912119954 hasRelatedWork W2183352214 @default.
• W2912119954 hasRelatedWork W2403286405 @default.
• W2912119954 hasRelatedWork W2626032497 @default.
• W2912119954 hasRelatedWork W2802958025 @default.
• W2912119954 hasRelatedWork W2971343459 @default.
• W2912119954 hasRelatedWork W3027442846 @default.
• W2912119954 hasRelatedWork W3177898245 @default.
• W2912119954 hasRelatedWork W4292916892 @default.
• W2912119954 hasVolume "69" @default.
• W2912119954 isParatext "false" @default.
• W2912119954 isRetracted "false" @default.
• W2912119954 magId "2912119954" @default.
• W2912119954 workType "article" @default.