Evidence map›Paper›PMID 18632874›Full record

ArticleJournal of molecular endocrinology2008

Comparative effects of estradiol, methyl-piperidino-pyrazole, raloxifene, and ICI 182 780 on gene expression in the murine uterus.

Angela M Davis, Jiude Mao, Bushra Naz, Jessica A Kohl, Cheryl S Rosenfeld

Abstract readComparative Study
In one paragraph

Article in Journal of molecular endocrinology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

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

14 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  9. The role of S6K1 in ER-positive breast cancer.Cell cycle (Georgetown, Tex.) · 2012
    Article
  10. Review
  11. Article
  12. Article
  13. Contrasting effects of different maternal diets on sexually dimorphic gene expression in the murine placenta.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  14. 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

5 authors.

Angela M DavisDepartment of Biomedical Sciences, 440F Christopher S. Bond Life Sciences Center, University of Missouri, Columbia, Missouri 65211, USA.
Jiude Mao
Bushra Naz
Jessica A Kohl
Cheryl S Rosenfeld

Funding

Interferon and Raloxifene Effects on Cancer CellsK01CA096664 · NCI · UNIVERSITY OF MISSOURI-COLUMBIA · PI ROSENFELD, CHERYL SUSAN · 2003 to 2007
$708k
NCI NIH HHS CA96664NCI NIH HHS K01 CA096664
6 · The paper itself

Abstract

Selective estrogen receptor modulators (SERMs) are potentially useful in treating various endometrial disorders, including endometrial cancer, as they block some of the detrimental effects of estrogen. It remains unclear whether each SERM regulates a unique subset of genes and, if so, whether the combination of a SERM and 17beta-estradiol has an additive or synergistic effect on gene expression. We performed microarray analysis with Affymetrix Mouse Genome 430 2.0 short oligomer arrays to determine gene expression changes in uteri of ovariectomized mice treated with estradiol (low and high dose), methyl-piperidino-pyrazole (MPP), ICI 182 780, raloxifene, and combinations of high dose of estradiol with one of the SERM and dimethyl sulfoxide (DMSO) vehicle control. The nine treatments clustered into two groups, with MPP, raloxifene, and high dose of estradiol in one, and low dose of estradiol, ICI + estradiol, ICI, MPP + estradiol, and raloxifene + estradiol in the second group. Surprisingly, combining a high dose of estradiol with a SERM markedly increased (P<0.02) the number of regulated genes compared with each individual treatment. Analysis of expression for selected genes in uteri of estradiol and SERM-treated mice by quantitative (Q)RT-PCR generally supported the microarray results. For some cancer-associated genes, including Klk1, Ihh, Cdc45l, and Cdca8, administration of MPP or raloxifene with estradiol resulted in greater expression than estradiol alone (P<0.05). By contrast, ICI 182 780 suppressed more genes governing DNA replication compared with MPP and raloxifene treatments. Therefore, ICI 182 780 might be superior to MPP and raloxifene to treat estrogen-induced endometrial cancer in women.

Indexed as

AnimalsEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensFemaleFulvestrantGene ExpressionMiceOligonucleotide Array Sequence AnalysisOvariectomyPiperidinesPyrazolesRaloxifene HydrochlorideReverse Transcriptase Polymerase Chain ReactionUterus1,3-bis(4-hydroxyphenyl)-4-methyl-5-(4-(2-piperidinylethoxy)phenol)-1H-pyrazoleEstradiolEstrogen AntagonistsEstrogen Receptor alphaEstrogensFulvestrantPiperidinesPyrazolesRaloxifene Hydrochloride

Identifiers

PMID18632874
PMCPMC6697483

What OpenQuestion holds

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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.