Evidence map›Paper›PMID 19545149›Full record

ArticleJournal of proteome research2009

Rapid label-free identification of estrogen-induced differential protein expression in vivo from mouse brain and uterine tissue.

Laszlo Prokai, Stanley M Stevens, Navin Rauniyar, Vien Nguyen

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  3. Comparative Proteomics Analysis Reveals Unique Early Signaling Response ofInternational journal of molecular sciences · 2020
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  13. Recent advances in quantitative neuroproteomics.Methods (San Diego, Calif.) · 2013
    Review
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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

4 authors at 2 institutions in 1 country.

Laszlo ProkaiDepartment of Molecular Biology and Immunology, University of North Texas Health Science Center, Fort Worth, 76107, USA. lprokai@hsc.unt.edu
Stanley M Stevens
Navin Rauniyar
Vien Nguyen
University of North Texas · USUniversity of North Texas Health Science Center · US

Funding

ROLE OF MITHOCHONDRIAL ERB IN NEURONAL VULNDERABILITY TO NEUROTOXIC STRESSP01AG027956 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI SINGH, MEHARVAN · 2007 to 2017
$11.3M
Survey of Age-Associated Carbonylation of Brain ProteinsR01AG025384 · NIA · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI PROKAI, LASZLO · 2004 to 2008
$1.4M
The Role of Quinols in Estrogen NeuroprotectionR01NS044765 · NINDS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI PROKAI, LASZLO · 2003 to 2006
$1.3M
NIA NIH HHS AG025384NIA NIH HHS AG027956NIA NIH HHS P01 AG027956NIA NIH HHS R01 AG025384NINDS NIH HHS NS044765NINDS NIH HHS R01 NS044765
6 · The paper itself

Abstract

Protein abundance profiling from tissue using liquid chromatography-tandem mass spectrometry-based "shotgun" proteomics and label-free relative quantitation was evaluated for the investigation of estrogen-regulated protein expression in the mouse brain and uterus. Sample preparation involved a 30-min protein extraction in 8 M aqueous urea solution, followed by disulfide reduction, thiol alkylation, and trypsin digestion of the extracted proteins, and was performed on 3-4 mg of tissue to evaluate the suitability of this methodology to expedite the survey of cellular pathways that are affected in vivo by an experimental therapeutic intervention in an animal model. The label-free proteomic approach (spectral counting) was suitable to identify even subtle changes in cortical protein levels and revealed significant estrogen-induced upregulation of ATP synthase (both alpha- and beta-isoforms), aspartate aminotransferase 2, and mitochondrial malate dehydrogenase without any prior subcellular fractionation of the tissue or the use of multidimensional chromatographic separation. The methodology was also suitable to observe various up- and downregulated proteins in the uterine tissue of ovariectomized mice upon treatment with 17beta-estradiol. In addition to confirming a very significant decrease in the abundance of glutathione S-transferase recognized as a marker of estrogen's impact, our studies have also revealed potential new protein markers such as desmin and lumican that are critical components of cytoskeletal arrangement and, hence, regulation of their abundance could contribute to major morphological changes in the uterus occurring upon estrogenic stimulation.

Indexed as

Amino Acid SequenceAnimalsBrainBrain ChemistryChromatography, LiquidEstradiolEstrogensFemaleMiceMolecular Sequence DataProtein BiosynthesisProteomeProteomicsReproducibility of ResultsTandem Mass SpectrometryUterusEstradiolEstrogensProteome

Identifiers

PMID19545149
PMCPMC2771330
OpenAlexW1987280274

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.