ReviewFrontiers in cell and developmental biology2026
GPCRs as key regulators in wound healing.
Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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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
2 citing papers in PubMed.
- CB2 Receptor Activation Attenuates IL-1β-Induced Inflammatory Transcriptomic Networks in Human Gingival Fibroblasts.Pharmaceuticals (Basel, Switzerland) · 2026Article
- Immune dysregulation and postoperative wound complications in systemic autoimmune rheumatic diseases: toward disease-specific risk stratification.Frontiers in immunology · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Wound healing is a complex tissue repair process that occurs through a series of overlapping phases, regulated by various cell types and corresponding signaling molecules, including G-protein-coupled receptors (GPCRs). GPCRs are a large family of cell surface receptors that respond to a variety of external signals and significant targets in the design of novel drugs for a wide range of human diseases. They play vital roles throughout the different stages of wound healing. Specifically, GPCRs are essential for the recruitment of immune cells and the activation of signaling cascades related to epidermal cell proliferation and differentiation, including Hedgehog-GLI, Hippo-YAP1, and Wnt/β-catenin pathways. Modifying GPCR activity through agonists or antagonists can alter GPCR signaling pathways, potentially affecting immune cell infiltration, the production of inflammatory mediators, and wound healing rates. This review summarizes the fundamental mechanisms of GPCR signaling pathways in wound healing and highlights recent discoveries regarding the roles and functions of GPCRs in this process.
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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.