Evidence map›Paper›PMID 39651565›Full record

ArticleCurrent computer-aided drug design2025

Insights into the Molecular Mechanisms of Bushen Huoxue Decoction in Breast Cancer

Hongyi Liang, Guoliang Yin, Guangxi Shi, Xiaofei Liu, Zhiyong Liu, Jingwei Li

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Article in Current computer-aided drug design, 2025. 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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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Hongyi LiangShandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Guoliang YinShandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Guangxi ShiAffiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Xiaofei LiuAffiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Zhiyong LiuAffiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jingwei LiAffiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

Funding

National Natural Science Foundation of China 82374452, 81573989, 81403408Natural Science Foundation of Shandong Province, China ZR2020QH337, ZR2020MH356
6 · The paper itself

Abstract

aimsBreast cancer (BC) is by far seen as the most common malignancy globally, with 2.261 million patients newly diagnosed, accounting for 11.7% of all cancer patients, according to the Global Cancer Statistics Report (2020). The luminal A subtype accounts for at least half of all BC diagnoses. According to TCM theory, Bushen Huoxue Decoction (BSHXD) is a prescription used for cancer treatment that may influence luminal A subtype breast cancer (LASBC).

objectivesTo analyze the clinical efficacy and underlying mechanisms of BSHXD in LASBC. MATERIALS AND

methodsNetwork pharmacology and

resultsAccording to the bioinformatics analysis, BSHXD induced several proliferation and apoptosis processes against LASBC, and the presumed targets of active components in BSHXD were mainly enriched in the HIF-1 and PI3K/AKT pathways. Flow cytometry assay and western blotting results revealed that the rate of apoptosis enhanced in a dose-dependent manner with BSHXD concentration increasing, respectively. BSHXD notably downregulated the expressions of HIF-1α, P-PI3K, PI3K, P-AKT and AKT proteins. However, adding an HIF-1α agonist restored those protein levels.

conclusionThe study proved that the mechanism of BSHXD in LASBC may be connected to suppressing proliferation by inhibiting the activity of the HIF-1α/PI3K/AKT signaling pathway and promoting apoptosis via the Caspase cascade in LASBC cells.

Indexed as

ApoptosisBreast NeoplasmsCell ProliferationDrugs, Chinese HerbalNetwork PharmacologyAntineoplastic Agents, PhytogenicCell Line, TumorDose-Response Relationship, DrugFemaleHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionAntineoplastic Agents, PhytogenicDrugs, Chinese HerbalPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktBushen huoxue decoctioncell apoptosiscell proliferationin vitro experiments.luminal A subtype breast cancernetwork 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 OpenQuestion graph.