Evidence map›Paper›PMID 25840272›Full record

ArticleAmerican journal of obstetrics and gynecology2015

Novel effects of simvastatin on uterine fibroid tumors: in vitro and patient-derived xenograft mouse model study.

Mostafa A Borahay, Kathleen Vincent, Massoud Motamedi, Elena Sbrana, Gokhan S Kilic, Ayman Al-Hendy, Darren Boehning

Abstract read
In one paragraph

Article in American journal of obstetrics and gynecology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

32 citing papers in PubMed, 48 citations in OpenAlex.

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  4. Simvastatin-loaded liposomal nanoparticles as treatment for adenomyosis in a patient-derived xenograft mouse model: a pilot study.Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology · 2025
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  14. Simvastatin-loaded liposome nanoparticles treatment for uterine leiomyoma in a patient-derived xenograft mouse model: a pilot study.Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology · 2022
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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

7 authors at 3 institutions in 1 country.

Mostafa A BorahayDepartment of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX; Department of Biochemistry and Molecular Biology, University of Texas Health Sciences Center at Houston, Houston, TX. Electronic address: maboraha@utmb.edu.
Kathleen VincentDepartment of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX; Biomedical Engineering Center, University of Texas Medical Branch, Galveston, TX.
Massoud MotamediBiomedical Engineering Center, University of Texas Medical Branch, Galveston, TX.
Elena SbranaDepartment of Pathology, University of Texas Medical Branch, Galveston, TX.
Gokhan S KilicDepartment of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX.
Ayman Al-HendyDepartment of Obstetrics and Gynecology, Georgia Regents University, Augusta, GA.
Darren BoehningDepartment of Biochemistry and Molecular Biology, University of Texas Health Sciences Center at Houston, Houston, TX.
The University of Texas Medical Branch at Galveston · USAugusta University · USThe University of Texas Health Science Center at Houston · US

Funding

UTMB Clinical and Translational Science AwardUL1TR001439 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI URBAN, RANDALL J · 2015 to 2024
$40.0M
UTMB Clinical and Translational Science AwardUL1TR000071 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2012 to 2014
$14.4M
WOMEN'S REPRODUCTIVE HEALTH RESEARCH CENTERK12HD001269 · NICHD · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI HANKINS, GARY D · 1998 to 2013
$5.0M
Mechanisms of Apoptotic Calcium SignalingR01GM081685 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BOEHNING, DARREN F · 2007 to 2020
$4.3M
UTMB Clinical and Translational Science AwardKL2TR001441 · NCATS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI AMEREDES, BILL T · 2015 to 2024
$4.0M
NCATS NIH HHS KL2 TR001441NCATS NIH HHS UL1 TR000071NCATS NIH HHS UL1TR000071NCATS NIH HHS UL1 TR001439NICHD NIH HHS 5K12HD001269-12NICHD NIH HHS K12 HD001269NIGMS NIH HHS 1R01GM081685-01NIGMS NIH HHS 3R01GM081685-03S1NIGMS NIH HHS R01 GM081685
6 · The paper itself

Abstract

objectiveUterine leiomyomas represent a common gynecologic problem with no satisfactory long-term medical treatment. The purpose of this study is to examine the effects of simvastatin on uterine leiomyoma, both in vitro and in vivo. STUDY

designThis is a laboratory-based experimental study. For in vitro studies, we used human and rat leiomyoma cells. For in vivo studies, we used immunodeficient mice supplemented with estrogen/progesterone pellets xenografted with human leiomyoma tissue explant.

resultsFor in vitro studies, cells were treated with different concentrations of simvastatin for 48 hours. Simvastatin induced dose-dependent apoptosis in leiomyoma cells as measured by a fluorometric caspase-3 activity assay, and inhibited proliferation as demonstrated by an (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay (both were significant at 5 and 10 μM). In addition, simvastatin decreased Akt signaling pathway phosphorylation as examined using Western blot analysis. For in vivo studies, animals were treated for 28 days with simvastatin (20 μg/gm body weight/day) vs vehicle control. The treatment inhibited tumor growth as measured weekly using calipers and/ or ultrasound (P < .01). Finally, simvastatin decreased expression of the proliferation marker Ki67 in xenograft tumor tissue as examined by immunohistochemistry (P = .02).

conclusionSimvastatin can be a promising treatment for uterine leiomyoma. Further studies, including pharmacokinetic and drug delivery studies, are required.

Indexed as

AnimalsApoptosisCell Line, TumorCell ProliferationEstrogensFemaleHumansHydroxymethylglutaryl-CoA Reductase InhibitorsImmunohistochemistryIn Vitro TechniquesKi-67 AntigenLeiomyomaMicePhosphorylationProgesteroneProgestinsEstrogensHydroxymethylglutaryl-CoA Reductase InhibitorsKi-67 AntigenProgesteroneProgestinsProto-Oncogene Proteins c-aktSimvastatinleiomyomapatient-derived xenograft modelsimvastatintreatmenttumor

Identifiers

PMID25840272
PMCPMC4519389
OpenAlexW1987267629

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.