Evidence map›Paper›PMID 26402163›Full record

ArticleRedox biology2015

A short report: PAMM, a novel antioxidant protein, induced by oxidative stress.

Yan Xu, Leslie R Morse, Raquel Assed Bezerra da Silva, Dianhua Wang, Ricardo A Battaglino

Open access · goldAbstract read
In one paragraph

Article in Redox biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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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

5 authors at 3 institutions in 3 countries.

Yan XuDepartment of Mineralized Tissue Biology, The Forsyth Institute, 245 First Street, Cambridge, MA 02142, USA; School of Pharmaceutical Science, Kunming Medical University, 1168 West Chunrong Road, Kunming 650500, China. Electronic address: yxu@forsyth.org.
Leslie R MorseDepartment of Mineralized Tissue Biology, The Forsyth Institute, 245 First Street, Cambridge, MA 02142, USA; Spaulding-Harvard SCI Model System, Spaulding Rehabilitation Hospital, 300 1st Ave, Charlestown, MA 02129, USA; Department of Physical Medicine and Rehabilitation, Harvard Medical School, 25 Shattuck St, Boston, MA 02115, USA. Electronic address: leslie.morse@mgh.harvard.edu.
Raquel Assed Bezerra da SilvaDepartment of Pediatric Clinic, Preventive and Community Dentistry, School of Dentistry of Ribeirao Preto, University of Sao Paulo, Sao Paulo 05508, Brazil. Electronic address: raquel@forp.usp.br.
Dianhua WangSchool of Pharmaceutical Science, Kunming Medical University, 1168 West Chunrong Road, Kunming 650500, China. Electronic address: wangdianhuakm@126.com.
Ricardo A BattaglinoDepartment of Mineralized Tissue Biology, The Forsyth Institute, 245 First Street, Cambridge, MA 02142, USA; Department of Oral Medicine, Infection, and Immunity, Harvard School of Dental Medicine, 188 Longwood Ave, Boston, MA 02115, USA. Electronic address: rbattaglino@forsyth.or.
Harvard University · USKunming Medical University · CNUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reactive oxygen species (ROS) play a central role in estrogen deficiency-induced bone loss. We previously identified and characterized a novel member of the Peroxiredoxin (PRX) like 2 family that we called PAMM: Peroxiredoxin Activated in M-CSF stimulated Monocytes, a redox regulatory protein that modulates osteoclast differentiation in vitro. In this study, we report increased PAMM expression in H2O2-treated cells and in bones from ovariectomized (OVX) mice 4 weeks after surgery, models for oxidative stress in vitro and in vivo, respectively. We also detected increased PAMM abundance and phosphorylated Akt in OVX mice treated with estrogen. In addition, Wortmannin, a specific PI3Kinase inhibitor and Rapamycin, an inhibitor of the PI3Kinase/Akt pathway, blocked Akt phosphorylation and stimulation of PAMM expression by M-CSF. These results indicate that M-CSF-induced PAMM expression is mediated by Akt phosphorylation. Our data also suggest that estrogen-induced PAMM expression is mediated by phosphorylation of Akt. These findings point to PAMM as a potential candidate for Akt-mediated protection against oxidative stress.

Indexed as

Oxidative StressAnimalsAntioxidantsBone DensityCells, CulturedEstrogensFemaleHumansMacrophage Colony-Stimulating FactorMiceNF-E2-Related Factor 2OsteoclastsOvariectomyOxidation-ReductionPeroxiredoxinsPhosphorylationAntioxidantsEstrogensMacrophage Colony-Stimulating FactorNFE2L2 protein, humanNF-E2-Related Factor 2PeroxiredoxinsProto-Oncogene Proteins c-aktPRXL2A protein, humanAntioxidantBone lossOvariectomyOxidative stressPAMM

Identifiers

PMID26402163
PMCPMC4588419
OpenAlexW1864101775

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.