ArticleAnnals of vascular medicine and research2023
Role of Caspase-8 on Retinal Endothelial Cell Migration and Angiogenesis.
Article in Annals of vascular medicine and research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Caspase-9 Is a Positive Regulator of Osteoblastic Cell Migration Identified by diaPASEF Proteomics.Journal of proteome research · 2024Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Pathological angiogenesis is the hallmark of proliferative diabetic retinopathy (DR). In response to prolonged tissue injury, human retinal microvascular endothelial (HRMEC) cells form new blood vessels to ensure the supply of oxygen and nutrients; however, progressive fibrovascular proliferation can eventually lead to angiogenesis, retinal detachment, and blindness. Caspase-8, a responsible protease for apoptosis has also been shown to modulate pathological and developmental angiogenesis but whether it exerts this role in a hyperglycemic environment has not yet been explored. Here we demonstrate that high glucose decreased HRMEC cell viability and increased VEGF secretion. Pro-Caspase 8 expression was measured by RT-PCR and caspase 8 enzyme activity was confirmed by Caspase-Glo assay. In addition, Caspase-8 KD resulted in an inhibition of cell migration, and a significant reduction of p38 phosphorylation. Taken together, our data suggest that Caspase-8 may play a role in angiogenesis by promoting HRMEC migration via p38 MAPK phosphorylation.
Indexed as
Identifiers
42164054PMC13186181What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.