Evidence map›Paper›PMID 41896362›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2026

Hongwu mixture exerts inhibition on triple-negative breast cancer by regulating SAV1/Hippo signaling through ZNF143.

Aiping Wu, Jun Ma, Qiong Wang, Aifei Chen, Wenling Lv, Yu Zhang, Hongying Zhang

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 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

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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

7 authors.

Aiping Wu *Department of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China. Aiping73021@126.com.
Jun Ma *Department of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.
Qiong WangDepartment of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.
Aifei ChenDepartment of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.
Wenling LvDepartment of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.
Yu ZhangDepartment of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.
Hongying ZhangDepartment of Oncology, Huai'an TCM Hospital Affiliated to Nanjing University of Chinese Medicine, No.3, Heping Road, Qingjiangpu District, Huai'an, 223001, Jiangsu, P.R. China.

Funding

2023 Huai'an Municipal Basic Research Program (Joint Special Project) Health and Medical Research Projects HABL2023099
6 · The paper itself

Abstract

Hongwu mixture (HWM) consists of Taxus chinensis, Marsdenia tenacissima, Rhizoma Curcumae, and Semen coicis. The objective of this study was to ascertain the potential role of the Hongwu mixture (HWM) in the treatment of triple-negative breast cancer (TNBC). TNBC cells were treated with low, medium, and high doses of HWM, and CCK-8 assays were conducted to evaluate the impact of different doses of HWM on TNBC cell viability. The target molecules of HWM were predicted using RNA-sequencing, and molecular docking models between HWM components and target proteins were developed. As the dose of HWM increased, TNBC cell viability gradually decreased. HWM inhibited the proliferation and mobility of TNBC cells, slowed the tumor growth, and upregulated the apoptosis of TNBC cells. HWM promoted Zinc finger protein 143 (ZNF143)-mediated transcriptional activation of salvador family WW domain-containing protein 1 (SAV1) by stabilizing ZNF143 protein expression, leading to phosphorylation of large tumor suppressor homolog 1 (LATS1) and Yes-associated protein 1 (YAP1). Knockdown of ZNF143/SAV1 signaling impaired the therapeutic effect of HWM, and treatment with verteporfin, pharmacological inhibition of YAP/TAZ, reversed the effects of knockdown of SAV1. Therefore, HWM might offer a potent strategy for managing TNBC effectively.

Indexed as

Cell Cycle ProteinsDrugs, Chinese HerbalProtein Serine-Threonine KinasesSignal TransductionTrans-ActivatorsTriple Negative Breast NeoplasmsAnimalsApoptosisCell Line, TumorCell ProliferationCell SurvivalFemaleGene Expression Regulation, NeoplasticHumansMolecular Docking SimulationCell Cycle ProteinsDrugs, Chinese HerbalProtein Serine-Threonine KinasesTrans-Activators

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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.