Evidence map›Paper›PMID 25631045›Full record

ArticleThe Journal of biological chemistry2015

Sirtuin 1 is a negative regulator of parathyroid hormone stimulation of matrix metalloproteinase 13 expression in osteoblastic cells: role of sirtuin 1 in the action of PTH on osteoblasts.

Yurong Fei, Emi Shimizu, Michael W McBurney, Nicola C Partridge

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.1field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. The Roles of Epigenetics Regulation in Bone Metabolism and Osteoporosis.Frontiers in cell and developmental biology · 2020
    Review
  10. Regulation of Bone Remodeling by Parathyroid Hormone.Cold Spring Harbor perspectives in medicine · 2018
    Review
  11. Article
  12. Antcin-H Isolated fromEvidence-based complementary and alternative medicine : eCAM · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. PTH Signaling and Epigenetic Control of Bone Remodeling.Current molecular biology reports · 2016
    Article
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.

Yurong FeiFrom the Department of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York 10010 and.
Emi ShimizuFrom the Department of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York 10010 and.
Michael W McBurneythe Ottawa Health Research Center Institute, Ottawa, Ontario K1H 8L6, Canada.
Nicola C PartridgeFrom the Department of Basic Science and Craniofacial Biology, New York University College of Dentistry, New York, New York 10010 and ncp234@nyu.edu.
New York University · US

Funding

Nuclear Events in PTHR1 Action on BoneR01DK047420 · NIDDK · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI Nicola C Partridge · 1994 to 2026
$8.0M
NIDDK NIH HHS 5R01DK047420-20NIDDK NIH HHS R01 DK047420
6 · The paper itself

Abstract

Parathyroid hormone (PTH) is the only current anabolic treatment for osteoporosis in the United States. PTH stimulates expression of matrix metalloproteinase 13 (MMP13) in bone. Sirtuin 1 (SIRT1), an NAD-dependent deacetylase, participates in a variety of human diseases. Here we identify a role for SIRT1 in the action of PTH in osteoblasts. We observed increased Mmp13 mRNA expression and protein levels in bone from Sirt1 knock-out mice compared with wild type mice. PTH-induced Mmp13 expression was significantly blocked by the SIRT1 activator, resveratrol, in osteoblastic UMR 106-01 cells. In contrast, the SIRT1 inhibitor, EX527, significantly enhanced PTH-induced Mmp13 expression. Two h of PTH treatment augmented SIRT1 association with c-Jun, a component of the transcription factor complex, activator protein 1 (AP-1), and promoted SIRT1 association with the AP-1 site of the Mmp13 promoter. This binding was further increased by resveratrol, implicating SIRT1 as a feedback inhibitor regulating Mmp13 transcription. The AP-1 site of the Mmp13 promoter is required for PTH stimulation of Mmp13 transcriptional activity. When the AP-1 site was mutated, EX527 was unable to increase PTH-stimulated Mmp13 promoter activity, indicating a role for the AP-1 site in SIRT1 inhibition. We further showed that SIRT1 deacetylates c-Jun and that the cAMP pathway participates in this deacetylation process. These data indicate that SIRT1 is a negative regulator of MMP13 expression, SIRT1 activation inhibits PTH stimulation of Mmp13 expression, and this regulation is mediated by SIRT1 association with c-Jun at the AP-1 site of the Mmp13 promoter.

Indexed as

AcetylationAnimalsBinding SitesEnzyme InductionFemaleFemurGene ExpressionMaleMatrix Metalloproteinase 13Mice, Inbred C57BLMice, KnockoutOsteoblastsParathyroid HormonePromoter Regions, GeneticProtein BindingProtein Processing, Post-TranslationalMatrix Metalloproteinase 13Mmp13 protein, mouseParathyroid HormoneProto-Oncogene Proteins c-junSirt1 protein, mouseSirtuin 1Transcription Factor AP-1AP1 Transcription Factor (AP-1)Matrix Metalloproteinase (MMP)OsteoblastParathyroid HormonePTHSirtuin 1 (SIRT1)

Identifiers

PMID25631045
PMCPMC4375490
OpenAlexW99737864

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.