ReviewInternational journal of molecular sciences2026
Adipogenesis Under Leptin Control: Mechanisms and Model-Specific Effects.
Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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0 citing papers in PubMed.
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Authors and funding
6 authors.
Funding
Abstract
Adipogenesis is one way by which adipose tissue expands in our body. It is a complex tightly regulated process involving differentiation of mesenchymal stem cells (MSCs) into mature, lipid-containing adipocytes. One of the byproducts of this mechanism is leptin, an adipokine that plays a pivotal role in regulating food intake and energy homeostasis. While the increase in leptin secretion in proportion to fat mass expansion shows that leptin functions as a downstream marker of adipogenesis, emerging studies suggest that leptin itself may influence the adipogenesis process and act as a regulator. However, despite much research done to explore this, its role remains incompletely understood and often contradictory, with studies reporting pro-adipogenic, anti-adipogenic, or neutral effects depending on experimental context. These discrepancies highlight the influence of factors such as leptin concentration, timing of exposure, cell type, adipose depot, and species differences. This review gathers current evidence on leptin's role in adipogenesis, integrating findings from diverse experimental models and biological systems. We further examine the underlying molecular mechanisms and signaling pathways involved, aiming to clarify the context-dependent effects of leptin and identify key knowledge gaps to guide future research in adipose tissue biology and metabolic disease.
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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.