Evidence map›Paper›PMID 22933749›Full record

ArticleThe Journal of nutrition2012

Endogenous and exogenous equol are antiestrogenic in reproductive tissues of apolipoprotein e-null mice.

Fitriya N Dewi, Charles E Wood, Johanna W Lampe, Meredith A J Hullar, Adrian A Franke, Deborah L Golden, Michael R Adams, J Mark Cline

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of nutrition, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. The effect of chronic inflammation on female fertility.Reproduction (Cambridge, England) · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Frontiers in endocrinology · 2017
    Article
  7. Review
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 3 institutions in 2 countries.

Fitriya N DewiDepartment of Pathology, Section on Comparative Medicine, Wake Forest School of Medicine, Winston Salem, NC, USA.
Charles E Wood
Johanna W Lampe
Meredith A J Hullar
Adrian A Franke
Deborah L Golden
Michael R Adams
J Mark Cline
Wake Forest University · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAUniversity of Hawaiʻi at Mānoa · US

Funding

University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI Xin Chen · 1996 to 2026
$56.2M
SOY AND ESTROGEN INTERACTIONS IN THE BREASTR01AT000639 · NCCIH · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI CLINE, J. MARK · 2000 to 2009
$4.7M
DIETARY SOY SUPPLEMENTS: CARDIOPROTECTIVE MECHANISMSR01HL064746 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ADAMS, MICHAEL R · 2000 to 2008
$2.1M
NCCIH NIH HHS NIH R01 AT00639NCCIH NIH HHS R01 AT000639NCI NIH HHS P30 CA071789NHLBI NIH HHS R01 HL064746NHLBI NIH HHS R01 HL64746
6 · The paper itself

Abstract

Equol is an isoflavone (IF) metabolite produced by intestinal microbiota in a subset of people consuming dietary soy. Equol producers may show different responses to soy foods and phenotypes related to cancer risk. Here, we assessed the effects of soy IF, endogenous microbial equol production, and dietary racemic equol in a 3 × 2 × 2 factorial experiment using gnotobiotic apoE-null mice (n = 9-11/group/sex). At age 3-6 wk, equol-producing microbiota were introduced to one-half of the colony (n = 122). At age 6 wk, mice were randomized to receive a diet that contained 1 of 3 protein sources: casein and lactalbumin, alcohol-washed soy protein (low IF), and intact soy protein (high IF), with total IF amounts of 0, 42, and 566 mg/kg diet, respectively. One-half of each diet group also received racemic equol (291 mg/kg diet). After 16 wk of dietary treatment, serum isoflavonoid profiles varied with sex, soy IF amount, and intestinal microbiota status. There were no treatment effects on tissues of male mice. In females, reproductive tissue phenotypes differed by equol-producing ability (i.e., microbiota status) but not dietary equol or IF content. Equol producers had lower uterine weight, vaginal epithelial thickness, total uterine area, endometrial area, and endometrial luminal epithelial height compared with nonproducers (P < 0.05 for all), with an association between microbiota status and estrous cycle (P > chi-square = 0.03). Exogenous equol reduced expression of progesterone receptor (PGR) and the proliferation marker Ki67 (P < 0.0001) in vaginal epithelium and endometrium; for endogenous equol, only PGR was reduced (P < 0.0005). Our findings indicate that equol diminishes estrogen-dependent tissue responses in apoE-null mice.

Indexed as

AnimalsApolipoproteins ECaseinsDietEndometriumEquolEstrogen AntagonistsEstrogensFemaleImmunohistochemistryIntestinal MucosaIntestinesLactalbuminMaleMetagenomeMiceApolipoproteins ECaseinsEquolEstrogen AntagonistsEstrogensLactalbuminPhytoestrogensSoybean Proteins

Identifiers

PMID22933749
PMCPMC3442795
OpenAlexW2108062646

What OpenQuestion holds

Textmetadata
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.