Evidence map›Paper›PMID 30640711›Full record

ArticleEndocrine-related cancer2019

Effects of Jaeumkanghwa-tang on tamoxifen responsiveness in preclinical ER+ breast cancer model.

Fabia De Oliveira Andrade, Wei Yu, Xiyuan Zhang, Elissa Carney, Rong Hu, Robert Clarke, Kevin FitzGerald, Leena Hilakivi-Clarke

Open access · hybridAbstract read
In one paragraph

Article in Endocrine-related cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 45% of its field
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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

8 authors at 2 institutions in 1 country.

Fabia De Oliveira AndradeDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Wei YuDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Xiyuan ZhangDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Elissa CarneyDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Rong HuDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Robert ClarkeDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Kevin FitzGeraldDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
Leena Hilakivi-ClarkeDepartment of Oncology, Georgetown University, Washington, District of Columbia, USA.
National Cancer Institute · USNational Institutes of Health · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI Louis M Weiner · 1990 to 2026
$71.5M
Collaborative Research in Integrative Cancer BiologyU01CA184902 · NCI · GEORGETOWN UNIVERSITY · PI CLARKE, ROBERT R., WANG, YUE · 2014 to 2018
$2.7M
Transgenerational effects of maternal high fat diet during pregnancy on breast caR01CA164384 · NCI · GEORGETOWN UNIVERSITY · PI HILAKIVI-CLARKE, LEENA A. · 2012 to 2015
$2.0M
NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA164384NCI NIH HHS U01 CA184902
6 · The paper itself

Abstract

Resistance to endocrine therapy remains a clinical challenge in the treatment of estrogen receptor-positive (ER+) breast cancer. We investigated if adding a traditional Asian herbal mixture consisting of 12 herbs, called Jaeumkanghwa-tang (JEKHT), to tamoxifen (TAM) therapy might prevent resistance and recurrence in the ER+ breast cancer model of 7,12-dimethylbenz[a]anthracene (DMBA)-exposed Sprague-Dawley rats. Rats were divided into four groups treated as follows: 15 mg/kg TAM administered via diet as TAM citrate (TAM only); 500 mg/kg JEKHT administered via drinking water (JEKHT only group); TAM + JEKHT and no treatment control group. The study was replicated using two different batches of JEKHT. In both studies, a significantly higher proportion of ER+ mammary tumors responded to TAM if animals also were treated with JEKHT (experiment 1: 47% vs 65%, P = 0.015; experiment 2: 43% vs 77%, P < 0.001). The risk of local recurrence also was reduced (31% vs 12%, P = 0.002). JEKHT alone was mostly ineffective. In addition, JEKHT prevented the development of premalignant endometrial lesions in TAM-treated rats (20% in TAM only vs 0% in TAM + JEKHT). Co-treatment of antiestrogen-resistant LCC9 human breast cancer cells with 1.6 mg/mL JEKHT reversed their TAM resistance in dose-response studies in vitro. Several traditional herbal medicine preparations can exhibit anti-inflammatory properties and may increase anti-tumor immune activities in the tumor microenvironment. In the tumors of rats treated with both JEKHT and TAM, expression of Il-6 (P = 0.03), Foxp3/T regulatory cell (Treg) marker (P = 0.033) and Tgfβ1 that activates Tregs (P < 0.001) were significantly downregulated compared with TAM only group. These findings indicate that JEKHT may prevent TAM-induced evasion of tumor immune responses.

Indexed as

9,10-Dimethyl-1,2-benzanthraceneAnimalsAntineoplastic Agents, HormonalBreast NeoplasmsCell Line, TumorCell ProliferationCytokinesDrug Resistance, NeoplasmEndometriumEstrogen AntagonistsFemaleForkhead Transcription FactorsHumansMammary Neoplasms, ExperimentalMedicine, East Asian TraditionalNeoplasm Recurrence, Local9,10-Dimethyl-1,2-benzanthraceneAntineoplastic Agents, HormonalCytokinesEstrogen AntagonistsForkhead Transcription FactorsFoxp3 protein, ratPlant ExtractsReceptors, EstrogenTamoxifenTgfb1 protein, ratTransforming Growth Factor beta1breast cancerendometrial atypical hyperplasiaJaeumkanghwa-tangpreclinicaltamoxifen

Identifiers

PMID30640711
PMCPMC6365679
OpenAlexW2910788216

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LicenceCC BY
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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.