Evidence map›Paper›PMID 23281008›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2013

DNA damage drives accelerated bone aging via an NF-κB-dependent mechanism.

Qian Chen, Kai Liu, Andria R Robinson, Cheryl L Clauson, Harry C Blair, Paul D Robbins, Laura J Niedernhofer, Hongjiao Ouyang

Open access · bronzeAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

80 citing papers in PubMed, 125 citations in OpenAlex.

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20 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

8 authors at 3 institutions in 1 country.

Qian ChenDepartment of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Kai Liu
Andria R Robinson
Cheryl L Clauson
Harry C Blair
Paul D Robbins
Laura J Niedernhofer
Hongjiao Ouyang
UPMC Hillman Cancer Center · USUniversity of Pittsburgh · USVeterans Health Administration · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Jessie Nedrow · 1988 to 2026
$158.0M
VARIABILITY, STABILITY & SMOOTHNESS OF WALKINGP30AG024827 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JENNIFER S BRACH · 2004 to 2026
$28.6M
NF-kB Inhibition Therapy for Duchenne Muscular DystrophyU01NS058451 · NINDS · OHIO STATE UNIVERSITY · PI GUTTRIDGE, DENIS C · 2008 to 2012
$5.2M
The contribution of DNA interstrand crosslinks to agingR01ES016114 · NIEHS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIEDERNHOFER, LAURA JANE · 2007 to 2011
$2.5M
mTOR SIGNALING: A NOVEL MECHANISM OF WNT'S ANABOLIC EFFECTS ON BONER01DE017439 · NIDCR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OUYANG, HONGJIAO · 2006 to 2010
$1.8M
LMP and Bone HealingR01AR051456 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ROBBINS, PAUL D. · 2008 to 2012
$1.7M
Regulation of Human Bone Turnover by FSHR01AR055208 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BLAIR, HARRY COLBERT · 2008 to 2012
$1.6M
XBP1s and Resveratrol regulate the BMSCs'support of myeloma growth and osteoclastR21CA161150 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OUYANG, HONGJIAO · 2012 to 2013
$368k
Muscle stem cell therapy in a mouse model of premature agingR21AG033907 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUARD, JOHNNY · 2009 to 2010
$336k
NCI NIH HHS P30 CA047904NCI NIH HHS P30CA047904NCI NIH HHS R21 CA161150NCI NIH HHS R21CA161150NIAMS NIH HHS AR051456NIAMS NIH HHS R01 AR051456NIAMS NIH HHS R01 AR055208NIAMS NIH HHS R01AR055208NIA NIH HHS AG024827NIA NIH HHS AG033907NIA NIH HHS P30 AG024827NIA NIH HHS P30AG024827NIA NIH HHS R21 AG033907NIDCR NIH HHS R01 DE017439NIDCR NIH HHS R01DE017439NIEHS NIH HHS ES016114NIEHS NIH HHS R01 ES016114NINDS NIH HHS NS058451NINDS NIH HHS U01 NS058451
6 · The paper itself

Abstract

Advanced age is one of the most important risk factors for osteoporosis. Accumulation of oxidative DNA damage has been proposed to contribute to age-related deregulation of osteoblastic and osteoclastic cells. Excision repair cross complementary group 1-xeroderma pigmentosum group F (ERCC1-XPF) is an evolutionarily conserved structure-specific endonuclease that is required for multiple DNA repair pathways. Inherited mutations affecting expression of ERCC1-XPF cause a severe progeroid syndrome in humans, including early onset of osteopenia and osteoporosis, or anomalies in skeletal development. Herein, we used progeroid ERCC1-XPF-deficient mice, including Ercc1-null (Ercc1(-/-)) and hypomorphic (Ercc1(-/Δ)) mice, to investigate the mechanism by which DNA damage leads to accelerated bone aging. Compared to their wild-type littermates, both Ercc1(-/-) and Ercc1(-/Δ) mice display severe, progressive osteoporosis caused by reduced bone formation and enhanced osteoclastogenesis. ERCC1 deficiency leads to atrophy of osteoblastic progenitors in the bone marrow stromal cell (BMSC) population. There is increased cellular senescence of BMSCs and osteoblastic cells, as characterized by reduced proliferation, accumulation of DNA damage, and a senescence-associated secretory phenotype (SASP). This leads to enhanced secretion of inflammatory cytokines known to drive osteoclastogenesis, such as interleukin-6 (IL-6), tumor necrosis factor α (TNFα), and receptor activator of NF-κB ligand (RANKL), and thereby induces an inflammatory bone microenvironment favoring osteoclastogenesis. Furthermore, we found that the transcription factor NF-κB is activated in osteoblastic and osteoclastic cells of the Ercc1 mutant mice. Importantly, we demonstrated that haploinsufficiency of the p65 NF-κB subunit partially rescued the osteoporosis phenotype of Ercc1(-/Δ) mice. Finally, pharmacological inhibition of the NF-κB signaling via an I-κB kinase (IKK) inhibitor reversed cellular senescence and SASP in Ercc1(-/Δ) BMSCs. These results demonstrate that DNA damage drives osteoporosis through an NF-κB-dependent mechanism. Therefore, the NF-κB pathway represents a novel therapeutic target to treat aging-related bone disease.

Indexed as

DNA DamageAnimalsBone and BonesCell DifferentiationCells, CulturedDNA-Binding ProteinsEndonucleasesMiceMice, KnockoutNF-kappa BOsteoblastsOsteoporosisDNA-Binding ProteinsEndonucleasesErcc1 protein, mouseNF-kappa B

Identifiers

PMID23281008
PMCPMC3662975
OpenAlexW2052845629

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Registered trials

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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.