AI Article Synopsis

  • Umbelliferone (UMB), a plant-derived compound, has shown potential pharmacological properties, but its effects on benign prostatic hyperplasia (BPH) were previously unclear.
  • A recent study investigated UMB's anti-proliferative effects on BPH-1 cells and its impact on testosterone-induced BPH in rats, revealing that UMB alters the STAT3/E2F1 signaling pathway.
  • Results indicated that UMB reduced prostate size and weight in rats, inhibited specific markers associated with cell proliferation, and suggested UMB could be a potential treatment for BPH.

Article Abstract

Umbelliferone (UMB), also known as 7-hydroxycoumarin, is a derivative of coumarin, which is widely found in many plants such as carrots, coriander, and garden angelica. Although many studies have already revealed the various pharmacological properties of UMB, its effect on benign prostatic hyperplasia (BPH) remains unclear. Therefore, the present study aimed to elucidate the underlying mechanism of the anti-proliferative effect of UMB in a human benign prostatic hyperplasia cell line (BPH-1), as well as its ameliorative effect on BPH in testosterone propionate (TP)-induced rats. The results showed that UMB exerts an anti-proliferative effect in BPH-1 cells by modulating the signal transducer and activator of transcription 3 (STAT3)/E2F transcription factor 1 (E2F1) axis. UMB treatment not only inhibited androgen/androgen receptor (AR) signaling-related markers, but also downregulated the overexpression of G1/S phase cell cycle-related markers. In TP-induced rats, UMB administration demonstrated an anti-BPH effect by significantly reducing prostate size, weight, and epithelial thickness. In addition, UMB suppressed cell proliferation by reducing the expression of proliferating cell nuclear antigen (PCNA) and p-STAT3 (Tyr 705) in prostate tissue following TP injection. These findings suggest that UMB has pharmacological effects against BPH.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8396462PMC
http://dx.doi.org/10.3390/ijms22169019DOI Listing

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