Evidence map›Paper›PMID 41946659›Full record

ArticleThe world journal of men's health2026

A Novel

Hyo-Jung Kim, Bo-Ram Jin, Sa-Haeng Kang, Jong-Sik Jin, Dong-Gu Kim, Jeonghoon Lee, Wonnam Kim, Jong-Hyun Lee, Hyo-Jin An

Abstract read
In one paragraph

Article in The world journal of men's health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Hyo-Jung KimCollege of Pharmacy and Institute of Integrated Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea.ORCID https://orcid.org/0009-0002-0696-1980
Bo-Ram JinCollege of Pharmacy and Institute of Integrated Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea.ORCID https://orcid.org/0000-0002-3635-034X
Sa-Haeng KangDepartment of Oriental Medicine Resources, Jeonbuk National University, Iksan, Korea.ORCID https://orcid.org/0009-0004-7776-8875
Jong-Sik JinDepartment of Oriental Medicines and LED Agri-bio Fusion Technology Research Center, Jeonbuk National University, Iksan, Korea.ORCID https://orcid.org/0000-0002-1387-6226
Dong-Gu KimDepartment of Herbology, College of Korean Medicine, Dong-Eui University, Busan, Korea.ORCID https://orcid.org/0009-0007-0137-904X
Jeonghoon LeeIndustrial Crop Breeding Division, National Institute of Horticultural and Herbal Science, Rural Development Administration, Eumseong, Korea.ORCID https://orcid.org/0000-0001-6709-5508
Wonnam KimDivision of Pharmacology, School of Korean Medicine, Pusan National University, Yangsan, Korea.ORCID https://orcid.org/0000-0002-5604-7532
Jong-Hyun LeeDepartment of Pharmacy, College of Pharmacy, Dongduk Women's University, Seoul, Korea.ORCID https://orcid.org/0000-0002-3193-8152
Hyo-Jin AnCollege of Pharmacy and Institute of Integrated Pharmaceutical Sciences, Kyung Hee University, Seoul, Korea. hjan@khu.ac.kr.ORCID https://orcid.org/0000-0002-2937-874X

Funding

Kyung Hee University KHU-20233259
6 · The paper itself

Abstract

purposeIn traditional Chinese medicine, benign prostatic hyperplasia (BPH) is attributed to MATERIALS AND

methodsNetwork pharmacology was applied to identify potential molecular targets and pathways, and the predicted mechanisms were experimentally validated in BPH-1 cells and in rats with testosterone propionate (TP)-induced BPH.

resultsWG alleviated prostate enlargement in rats with TP-induced BPH. Network pharmacology predicted that WG could modulate key regulators of cell cycle progression and apoptosis. Consistently, WG suppressed androgen receptor (AR) signaling in both BPH-1 cells and rats with TP-induced BPH. WG also inhibited G1/S checkpoint regulators and induced apoptosis by reducing B-cell lymphoma (Bcl)-2 and Bcl-xL/Bcl-2 associated X protein ratios, leading to the activation of caspase-9 and -3. Through these actions, WG prevented the activation of the AR signaling pathway, promoted cell cycle arrest, and triggered apoptosis, thereby mitigating BPH progression.

conclusionsThese findings, supported by both network pharmacology predictions and experimental data, suggest that WG has promising therapeutic potential for the treatment of BPH.

Indexed as

AndrogensApoptosisCell cycleGlycyrrhizaNetwork pharmacologyProstatic hyperplasia

Identifiers

PMID41946659
PMCPMC13302975

What OpenQuestion holds

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Registered trials

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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.