Evidence map›Paper›PMID 11748267›Full record

ArticleThe Journal of clinical investigation2001

Antisense inhibition of macrophage inflammatory protein 1-alpha blocks bone destruction in a model of myeloma bone disease.

S J Choi, Y Oba, Y Gazitt, M Alsina, J Cruz, J Anderson, G D Roodman

Open access · greenAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

59 citing papers in PubMed, 206 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Multiple Myeloma and Bone: The Fatal Interaction.Cold Spring Harbor perspectives in medicine · 2018
    Review
  10. Review
  11. Myeloma and Bone Disease.Current osteoporosis reports · 2017
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  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

7 authors at 4 institutions in 1 country.

S J ChoiDepartment of Medicine/Hematology, University of Texas Health Science Center, San Antonio, Texas, USA.
Y Oba
Y Gazitt
M Alsina
J Cruz
J Anderson
G D Roodman
The University of Texas Health Science Center at San Antonio · USPalmetto Hematology Oncology · USTexas Tech University · USUniversity of South Florida · US

Funding

TUMORS EFFECTS ON THE SKELETONP01CA040035 · NCI · VANDERBILT UNIVERSITY · PI SUN, LUZHE · 1985 to 2010
$11.0M
OSTEOCLASTS FROM TRANSGENIC MICER01AR041336 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, GARSON DAVID · 1991 to 2009
$2.3M
DEVELOPMENTAL ASPECTS OF OSTEOCLAST FORMATION IN VITROR01AG013625 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, GARSON DAVID · 1995 to 2005
$1.3M
PATHOBIOLOGY OF THE OSTEOCLAST IN PAGETS DISEASER01AR044603 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI ROODMAN, G DAVID · 1998 to 2002
$792k
NCI NIH HHS CA40035NCI NIH HHS P01 CA040035NIAMS NIH HHS AR-41336NIAMS NIH HHS AR-44603NIAMS NIH HHS R01 AR041336NIAMS NIH HHS R01 AR044603NIA NIH HHS AG-13625NIA NIH HHS R01 AG013625
6 · The paper itself

Abstract

We recently identified macrophage inflammatory protein 1-alpha (MIP-1alpha) as a factor produced by multiple myeloma (MM) cells that may be responsible for the bone destruction in MM (1). To investigate the role of MIP-1alpha in MM bone disease in vivo, the human MM-derived cell line ARH was stably transfected with an antisense construct to MIP-1alpha (AS-ARH) and tested for its capacity to induce MM bone disease in SCID mice. Human MIP-1alpha levels in marrow plasma from AS-ARH mice were markedly decreased compared with controls treated with ARH cells transfected with empty vector (EV-ARH). Mice treated with AS-ARH cells lived longer than controls and, unlike the controls, they showed no radiologically identifiable lytic lesions. Histomorphometric analysis demonstrated that osteoclasts (OCLs) per square millimeter of bone and OCLs per millimeter of bone surface of AS-ARH mice were significantly less than in EV-ARH mice, and the percentage of tumors per total bone area was also significantly decreased. AS-ARH cells demonstrated decreased adherence to marrow stromal cells, due to reduced expression of the alpha(5)beta(1) integrin and diminished homing capacity and survival. These data support an important role for MIP-1alpha in cell homing, survival, and bone destruction in MM.

Indexed as

AnimalsAntigens, CDAntisense Elements (Genetics)Bone DiseasesCD18 AntigensChemokine CCL3Chemokine CCL4HumansIntegrin alpha5Integrin beta1Macrophage Inflammatory ProteinsMiceMice, SCIDMultiple MyelomaOsteoclastsAntigens, CDAntisense Elements (Genetics)CD18 AntigensChemokine CCL3Chemokine CCL4Integrin alpha5Integrin beta1Macrophage Inflammatory Proteins

Identifiers

PMID11748267
PMCPMC209465
OpenAlexW2044739735

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.