Evidence map›Paper›PMID 41879444›Full record

ArticleCurrent drug targets2026

Research on the Anti-breast Hyperplasia Mechanism of Liqi Sanjie Granules Based on Network Pharmacological Analysis and Experimental Verification.

Xionghui Hu, Xun Liu, Rensong Yan, Xianhai Li, You Zhou, Fei Chen, Min Xu, Cheng Xiao, Yi Wang, Zhang Wang and 5 more

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Article in Current drug targets, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

15 authors.

Xionghui HuDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Xun LiuDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Rensong YanDazhou Vocational College of Chinese Medicine, Dazhou, 635000, China.
Xianhai LiDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
You ZhouChengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
Fei ChenDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Min XuChengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
Cheng XiaoDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Yi WangDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Zhang WangChengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
Yao LiuDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Bingguang ZhongDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Xiaoqi HuDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Qing ZhouDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.
Tanjun WeiDazhou Hospital of Integrated Traditional and Western Medicine, Dazhou, 635000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast hyperplasia has become a major public health challenge due to changes in dietary patterns. However, there is still a lack of effective pharmacotherapy for Breast hyperplasia.

methodsThe chemical components of Liqi Sanjie Granules (LSG) were quantified through HPLC. Three key components were screened out by combining network pharmacology methods and experimental determination methods, whereas key components in sera were quantified through LC-MS. The potential molecular mechanisms of LSG and these three blood-entering chemicals for the treatment of breast hyperplasia were predicted by network pharmacology. Estradiol benzoate and progesterone were injected intramuscularly to establish a breast hyperplasia model. Serum estradiol (E2), progesterone (P), testosterone (T), and prolactin (PRT) were detected by ELISA. H&E was used in monitoring the hyperplasia of rat mammary gland tissues. Immunohistochemistry and RT-PCR were used to detect the protein and mRNA expression levels of estrogen receptors (ERs) and progesterone receptors (PR) in rat mammary glands.

resultsThe contents of seven components in LSG were quantified. After administration, the levels of paeoniflorin, glycyrrhizin, and ferulic acid were 280.16 ± 64.77, 101.87 ± 7.88, and 253.28 ± 17.64 μg per 200 μL, respectively. Network pharmacology studies have shown that LSG treats breast hyperplasia by acting on 63 targets in 36 signaling pathways, and the blood-entering chemicals of LSG involve 18 potential targets and 5 signaling pathways. Histopathological analysis revealed that rats in the LSG group had fewer mammary lobules and acini. Additionally, the proliferation of glandular epithelial cells was reduced. No significant changes were found in the serum levels of E2, P, PRT, and T in the LSG group. Concurrently, LSG can reduce the expression levels of PR protein and the mRNA of ESR1 and PGR in the rat mammary glands. DISCUSSION: This study suggests that the blood-entering chemicals paeoniflorin, glycyrrhizin, and ferulic acid may alleviate breast hyperplasia through decreasing the expression levels of ER, ESR1, and PGR in the mammary tissues, reducing the number of mammary lobules and alveoli, and inhibiting pathological changes in vacuolar degeneration, hyperplasia, and detachment of glandular epithelial cells.

conclusionsThis study quantitatively analysed the seven chemical components of LSG and determined the contents of paeoniflorin, glycyrrhizin, and ferulic acid in the medicated serum. Furthermore, it demonstrates that LSG improves breast hyperplasia by regulating ER and PR expression levels.

Indexed as

Drugs, Chinese HerbalHyperplasiaMammary Glands, AnimalAnimalsCoumaric AcidsDisease Models, AnimalEstradiolFemaleGlycosidesMonoterpenesNetwork PharmacologyProgesteroneRatsRats, Sprague-DawleyReceptors, EstrogenReceptors, ProgesteroneCoumaric AcidsDrugs, Chinese HerbalEstradiolestradiol 3-benzoateferulic acidGlycosidesMonoterpenespeoniflorinProgesteroneReceptors, EstrogenReceptors, Progesteronebreast hyperplasiadetermine contentLiqi sanjie granulesmechanismnetwork pharmacology

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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 Socratic graph.