Evidence map›Paper›PMID 26631549›Full record

ArticleSteroids2016

Licorice root components in dietary supplements are selective estrogen receptor modulators with a spectrum of estrogenic and anti-estrogenic activities.

Nittaya Boonmuen, Ping Gong, Zulfiqar Ali, Amar G Chittiboyina, Ikhlas Khan, Daniel R Doerge, William G Helferich, Kathryn E Carlson, Teresa Martin, Pawinee Piyachaturawat and 2 more

Abstract read
In one paragraph

Article in Steroids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  11. Development of an Improved Menopausal Symptom-Alleviating Licorice (Journal of microbiology and biotechnology · 2020
    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

12 authors at 4 institutions in 2 countries.

Nittaya BoonmuenDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States; Department of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Ping GongDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
Zulfiqar AliNational Center for Natural Products Research, University of Mississippi, Oxford, MS 38677, United States.
Amar G ChittiboyinaNational Center for Natural Products Research, University of Mississippi, Oxford, MS 38677, United States.
Ikhlas KhanNational Center for Natural Products Research, University of Mississippi, Oxford, MS 38677, United States.
Daniel R DoergeDivision of Biochemical Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR 72079, United States.
William G HelferichDepartment of Food Science and Human Nutrition, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
Kathryn E CarlsonDepartment of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
Teresa MartinDepartment of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
Pawinee PiyachaturawatDepartment of Physiology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand; Chakri Naruebodindra Medical Institute, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
John A KatzenellenbogenDepartment of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States.
Benita S KatzenellenbogenDepartment of Molecular and Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, United States. Electronic address: katzenel@illinois.edu.
University of Illinois Urbana-Champaign · USUniversity of Mississippi · USMahidol University · THNational Center for Toxicological Research · US

Funding

Research Training Program in Toxicology and Environmental HealthT32ES007326 · NIEHS · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI Jodi A. Flaws · 2000 to 2026
$8.7M
Pharmacokinetics, Bioavailability, and Metabolism/Daniel R. DoergeP50AT006268 · NCCIH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI HELFERICH, WILLIAM G · 2010 to 2015
$7.6M
MOLECULAR PROBES FOR STEROID RECEPTORSR37DK015556 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, JOHN A. · 1987 to 2012
$4.4M
Novel Ligands and Mechanisms to Achieve Selective Nuclear Receptor ActivityR01DK015556 · NIDDK · UNIVERSITY OF ILLINOIS URBANA-CHAMPAIGN · PI KATZENELLENBOGEN, JOHN A. · 1986 to 2016
$1.6M
NCCIH NIH HHS P50 AT006268NCCIH NIH HHS P50AT006268NIDDK NIH HHS DK015556NIDDK NIH HHS R01 DK015556NIDDK NIH HHS R37 DK015556NIEHS NIH HHS T32 ES007326
6 · The paper itself

Abstract

Licorice root extracts are often consumed as botanical dietary supplements by menopausal women as a natural alternative to pharmaceutical hormone replacement therapy. In addition to their components liquiritigenin (Liq) and isoliquiritigenin (Iso-Liq), known to have estrogenic activity, licorice root extracts also contain a number of other flavonoids, isoflavonoids, and chalcones. We have investigated the estrogenic activity of 7 of these components, obtained from an extract of Glycyrrhiza glabra powder, namely Glabridin (L1), Calycosin (L2), Methoxychalcone (L3), Vestitol (L4), Glyasperin C (L5), Glycycoumarin (L6), and Glicoricone (L7), and compared them with Liq, Iso-Liq, and estradiol (E2). All components, including Liq and Iso-Liq, have low binding affinity for estrogen receptors (ERs). Their potency and efficacy in stimulating the expression of estrogen-regulated genes reveal that Liq and Iso-Liq and L2, L3, L4, and L6 are estrogen agonists. Interestingly, L3 and L4 have an efficacy nearly equivalent to E2 but with a potency ca. 10,000-fold less. The other components, L1, L5 and L7, acted as partial estrogen antagonists. All agonist activities were reversed by the antiestrogen, ICI 182,780, or by knockdown of ERα with siRNA, indicating that they are ER dependent. In HepG2 hepatoma cells stably expressing ERα, only Liq, Iso-Liq, and L3 stimulated estrogen-regulated gene expression, and in all cases gene stimulation did not occur in HepG2 cells lacking ERα. Collectively, these findings classify the components of licorice root extracts as low potency, mixed ER agonists and antagonists, having a character akin to that of selective estrogen receptor modulators or SERMs.

Indexed as

Dietary SupplementsCarcinoma, HepatocellularCell ProliferationEstrogen AntagonistsEstrogensFemaleFlavanonesGene Expression Regulation, NeoplasticGlycyrrhizaHumansKi-67 AntigenLiver NeoplasmsMagnetic Resonance SpectroscopyMCF-7 CellsPlant ExtractsPlant RootsEstrogen AntagonistsEstrogensFlavanonesKi-67 AntigenliquiritigeninPlant ExtractsReceptors, EstrogenSelective Estrogen Receptor ModulatorsBotanical estrogensEstrogen receptorLicorice root estrogensSelective estrogen receptor modulator

Identifiers

PMID26631549
PMCPMC4714869
OpenAlexW2179344188

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.