Evidence map›Paper›PMID 15694777›Full record

ArticleJournal of the American Society for Mass Spectrometry2005

Ultrafiltration tandem mass spectrometry of estrogens for characterization of structure and affinity for human estrogen receptors.

Yongkai Sun, Chungang Gu, Xuemei Liu, Wenzhong Liang, Ping Yao, Judy L Bolton, Richard B van Breemen

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Society for Mass Spectrometry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 77 citations in OpenAlex.

  1. Article
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  8. Celecoxib influences steroid sulfonation catalyzed by human recombinant sulfotransferase 2A1.The Journal of steroid biochemistry and molecular biology · 2015
    Article
  9. Article
  10. Article
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  12. Recent developments in protein-ligand affinity mass spectrometry.Analytical and bioanalytical chemistry · 2011
    Review
  13. Article
  14. Article
  15. Article
  16. Article
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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 2 institutions in 1 country.

Yongkai SunDepartment of Medical Chemistry and Pharmacognosy, The University of Illinois College of Pharmacy, Chicago, Illinois 60612, USA.
Chungang Gu
Xuemei Liu
Wenzhong Liang
Ping Yao
Judy L Bolton
Richard B van Breemen
University of Illinois Chicago · USIllinois College · US

Funding

Van Breemen: Project 3; Botanical Dietary Supplements - Metabolism and Safety in Women (Van Breemen)P50AT000155 · NCCIH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PAULI, GUIDO F · 1999 to 2019
$30.4M
Biotransformation of Estrogens to Carcinogenic QuinoidsR01CA073638 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BOLTON, JUDY L. · 2001 to 2005
$1.5M
CORE MASS SPECTROMETRY RESOURCE FOR CANCER RESEARCHR24CA083124 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI VAN BREEMEN, RICHARD B · 1999 to 2003
$779k
NCCIH NIH HHS P50 AT000155NCCIH NIH HHS P50 AT00155NCI NIH HHS R01 CA073638NCI NIH HHS R01 CA73638NCI NIH HHS R24 CA83124
6 · The paper itself

Abstract

Although hormone replacement therapy (HRT) is used by post-menopausal women for the relief of menopausal symptoms and the potential reduction of osteoporosis, HRT also increases their risk of Alzheimer's disease, stroke, breast cancer, and endometrial cancer. Since the majority of these effects are associated primarily with estrogen binding to only one of the estrogen receptors (ER), new assays are needed that can more efficiently evaluate ER-binding and identify ligands selective for ER-alpha and ER-beta. High performance liquid chromatography-tandem mass spectrometry (LC-MS-MS) was combined with ultrafiltration as a new method to investigate the relative binding of compounds to the ERs and to evaluate the structures of these estrogens. Mixtures of estradiol and six equine estrogens, including equilin, equilenin, 8,9-dehydroestrone, and their 17beta-hydroxyl derivatives, were assayed simultaneously to determine their relative binding to human ER-alpha and ER-beta. Estrogens containing a 17beta-OH group were found to have higher relative affinities for the estrogen receptors than their ketone analogs. In addition, 17beta-EN showed selectivity for binding to ER-beta over ER-alpha. The results were compared to the IC50 values obtained by using a conventional radiolabled estradiol competitive binding assay. Finally, the utility of negative ion electrospray tandem mass spectrometry for the unambiguous identification of these estrogen isomers was investigated. Several characteristic recyclization pathways during tandem mass spectrometry were identified, which might be useful for distinguishing related estrogens.

Indexed as

AnimalsEstrogensHorsesHumansMolecular StructureReceptors, EstrogenSpectrometry, Mass, Electrospray IonizationUltrafiltrationEstrogensReceptors, Estrogen

Identifiers

PMID15694777
PMCPMC1780173
OpenAlexW2006495275

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.