Evidence map›Paper›PMID 25210448›Full record

ReviewClinical interventions in aging2014

Selective estrogen receptor modulators: tissue specificity and clinical utility.

Stephen Martinkovich, Darshan Shah, Sonia Lobo Planey, John A Arnott

Open access · goldAbstract readReview
In one paragraph

Review in Clinical interventions in aging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
11.2field-weighted citation impact, top 1% 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

122 citing papers in PubMed, 235 citations in OpenAlex.

  1. Trial
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  10. Improvement of Menopausal Symptoms byFood science & nutrition · 2025
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62 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Stephen MartinkovichDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
Darshan ShahDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
Sonia Lobo PlaneyDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
John A ArnottDepartment of Basic Sciences, The Commonwealth Medical College, Scranton, PA, USA.
Commonwealth Medical College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Selective estrogen receptor modulators (SERMs) are a diverse group of nonsteroidal compounds that function as agonists or antagonists for estrogen receptors (ERs) in a target gene-specific and tissue-specific fashion. SERM specificity involves tissue-specific expression of ER subtypes, differential expression of co-regulatory proteins in various tissues, and varying ER conformational changes induced by ligand binding. To date, the major clinical applications of SERMs are their use in the prevention and treatment of breast cancer, the prevention of osteoporosis, and the maintenance of beneficial serum lipid profiles in postmenopausal women. However, SERMs have also been found to promote adverse effects, including thromboembolic events and, in some cases, carcinogenesis, that have proven to be obstacles in their clinical utility. In this review, we discuss the mechanisms of SERM tissue specificity and highlight the therapeutic application of well-known and emergent SERMs.

Indexed as

FemaleHumansOrgan SpecificitySelective Estrogen Receptor ModulatorsSelective Estrogen Receptor Modulatorsestrogen receptorsselective estrogen receptor modulatorsSERMs

Identifiers

PMID25210448
PMCPMC4154886
OpenAlexW2027044981

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.