Evidence map›Paper›PMID 18218727›Full record

ArticleMolecular endocrinology (Baltimore, Md.)2008

High-mobility group box proteins modulate tumor necrosis factor-alpha expression in osteoclastogenesis via a novel deoxyribonucleic acid sequence.

Kosj Yamoah, Alina Brebene, Ramkumarie Baliram, Kenji Inagaki, Georgia Dolios, Ario Arabi, Rinosha Majeed, Hitoshi Amano, Rong Wang, Robert Yanagisawa and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular endocrinology (Baltimore, Md.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-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

32 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Structure and Functions of HMGB2 Protein.International journal of molecular sciences · 2023
    Review
  8. Independent Skeletal Actions of Pituitary Hormones.Endocrinology and metabolism (Seoul, Korea) · 2022
    Article
  9. Article
  10. Review
  11. Thyrotropin, Hyperthyroidism, and Bone Mass.The Journal of clinical endocrinology and metabolism · 2021
    Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. The danger from within: alarmins in arthritis.Nature reviews. Rheumatology · 2016
    Review
  19. Review
  20. Review
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

11 authors at 2 institutions in 2 countries.

Kosj YamoahDepartment of Medicine, Mount Sinai School of Medicine, New York, New York 10029, USA.
Alina Brebene
Ramkumarie Baliram
Kenji Inagaki
Georgia Dolios
Ario Arabi
Rinosha Majeed
Hitoshi Amano
Rong Wang
Robert Yanagisawa
Etsuko Abe
Icahn School of Medicine at Mount Sinai · USShowa University · JP

Funding

MASS SPECTROMETRY SHARED RESOURCER24CA088325 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI WANG, RONG · 2001 to 2005
$1.4M
MALD/ESI-Q-TOF Mass Spectrometer Shared InstrumentS10RR017802 · NCRR · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI WANG, RONG · 2003 to 2003
$500k
PROTEOMEX LTQ WORKSTATION SHARED INSTRUMENTATION: PROTEOMICSS10RR022415 · NCRR · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI WANG, RONG · 2006 to 2006
$424k
NCI NIH HHS CA88325NCI NIH HHS R24 CA088325NCRR NIH HHS RR017802NCRR NIH HHS RR022415NCRR NIH HHS S10 RR017802NCRR NIH HHS S10 RR022415NIAMS NIH HHS AR052258
6 · The paper itself

Abstract

We have previously shown that mice lacking the TSH receptor (TSHR) exhibit osteoporosis due to enhanced osteoclast formation. The fact that this enhancement is not observed in double-null mice of TSHR and TNFalpha suggests that TNFalpha overexpression in osteoclast progenitors (macrophages) may be involved. It is unknown how TNFalpha expression is regulated in osteoclastogenesis. Here, we describe a receptor activator for nuclear factor-kappaB ligand (RANKL)-responsive sequence (CCG AGA CAG AGG TGT AGG GCC), spanning from -157 to -137 bp of the 5'-flanking region of the TNFalpha gene, which functions as a cis-acting regulatory element. We further show how RANKL treatment stimulates the high-mobility group box proteins (HMGB) HMGB1 and HMGB2 to bind the RANKL-responsive sequence and up-regulates TNFalpha transcription. Exogenous HMGB elicits the expression of cytokines, including TNFalpha, as well as osteoclast formation. Conversely, TSH inhibits the expression of HMGB and TNFalpha and the formation of osteoclasts. These results suggest that HMGB play a pivotal role in osteoclastogenesis. We also show a direct correlation between the expression of HMGB and TNFalpha and osteoclast formation in TSHR-null mice and TNFalpha-null mice. Taken together, we conclude that HMGB and TNFalpha play critical roles in the regulation of osteoclastogenesis and the remodeling of bone.

Indexed as

AnimalsBlotting, WesternCell LineChromatin ImmunoprecipitationDNAElectrophoretic Mobility Shift AssayGene Expression RegulationHMGB ProteinsHumansMacrophagesMiceOsteoclastsPolymerase Chain ReactionPromoter Regions, GeneticRANK LigandTranscription, GeneticDNAHMGB ProteinsRANK LigandTumor Necrosis Factor-alpha

Identifiers

PMID18218727
PMCPMC2366181
OpenAlexW2090741825

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.