Evidence map›Paper›PMID 27267714›Full record

ArticleEndocrinology2016

Endometrial Cancer-Associated FGF18 Expression Is Reduced by Bazedoxifene in Human Endometrial Stromal Cells In Vitro and in Murine Endometrium.

Clare A Flannery, Andrew G Fleming, Gina H Choe, Hanyia Naqvi, Margaret Zhang, Anu Sharma, Hugh S Taylor

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Tissue selective estrogen complex (TSEC): a review.Menopause (New York, N.Y.) · 2018
    Review
  9. Article
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 at 1 institution in 1 country.

Clare A FlanneryObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Andrew G FlemingObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Gina H ChoeObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Hanyia NaqviObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Margaret ZhangObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Anu SharmaObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Hugh S TaylorObstetrics, Gynecology, and Reproductive Sciences (C.A.F., A.G.F., G.H.C., H.N., M.Z., H.S.T.), Yale School of Medicine, New Haven, Connecticut 06520; and Endocrinology and Metabolism (C.A.F., A.S.), Internal Medicine, Yale School of Medicine, New Haven, Connecticut 06520.
Yale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Tissue Factor and EmdometriosisU54HD052668 · NICHD · YALE UNIVERSITY · PI TAYLOR, HUGH SMITH · 2007 to 2011
$6.6M
Environmental Estrogen Induced Epigenetic Alteration of Uterine Stem CellsR01HD076422 · NICHD · YALE UNIVERSITY · PI TAYLOR, HUGH SMITH · 2012 to 2016
$2.0M
Effect of Insulin on Estrogen Receptor Alpha Activity in Human Endometrial CellsK08HD071010 · NICHD · YALE UNIVERSITY · PI FLANNERY, CLARE ANN · 2012 to 2016
$658k
NCATS NIH HHS UL1 TR001863NICHD NIH HHS K08 HD071010NICHD NIH HHS R01 HD076422NICHD NIH HHS U54 HD052668
6 · The paper itself

Abstract

Endometrial cancer develops during exposure to estrogen unopposed by progesterone. Traditional formulations for menopausal hormone therapy include a progestin in women with a uterus. However, progestin exposure increases breast cancer risk in postmenopausal women. Alternatives to progestin include bazedoxifene (BZA), a selective estrogen receptor modulator, which prevents estrogen induced endometrial hyperplasia in clinical trials. Molecular mechanisms responsible for BZA's antiproliferative effect are not fully elucidated. We profiled endometrial adenocarcinoma, hyperplasia, and normal proliferative endometrium for differential expression in genes known to be regulated by estrogens or progesterone. Fibroblast growth factor (FGF)18, a paracrine growth factor promoting epithelial proliferation, was significantly increased in adenocarcinoma. Progesterone represses FGF18 by inducing heart and neural crest derivatives expressed transcript 2 (HAND2) in stromal cells. Notably, we confirmed lower HAND2 mRNA in adenocarcinoma, along with higher FGF tyrosine kinase receptor 2 and E74-like factor 5, collectively promoting FGF18 activity. We hypothesized BZA reduces epithelial proliferation by inhibiting FGF18 synthesis in stromal cells. To determine whether BZA regulates FGF18, we treated primary stromal cells with BZA or vehicle. In vitro, BZA reduced FGF18, but did not affect, HAND2. CD1 female mice received either BZA, conjugated estrogen (CE), or combined BZA/CE for 8 weeks. CE-treated mice had nearly 3-fold higher FGF18 expression. In contrast, BZA-treated mice, alone or with CE, had similar FGF18 as controls. Unexpectedly, BZA, alone or with CE, reduced HAND2 more than 80%, differing from progesterone regulation. Reduction of FGF18 is a potential mechanism by which BZA reduces endometrial proliferation and hyperplasia induced by estrogens. However, BZA works independently of HAND2, revealing a novel mechanism for progestin-free hormone therapy in postmenopausal women.

Indexed as

AdultAgedAged, 80 and overAnimalsBasic Helix-Loop-Helix ProteinsCarcinoma, EndometrioidCase-Control StudiesCells, CulturedEndometrial HyperplasiaEndometrial NeoplasmsEndometriumFemaleFibroblast Growth FactorsGene Expression ProfilingHumansIndolesBasic Helix-Loop-Helix Proteinsbazedoxifenefibroblast growth factor 18Fibroblast Growth FactorsHAND2 protein, humanIndolesSelective Estrogen Receptor Modulators

Identifiers

PMID27267714
PMCPMC5045514
OpenAlexW2417018242

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.