Evidence map›Paper›PMID 17086356›Full record

ArticleClinical & experimental metastasis2006

Role of CCR1 and CCR5 in homing and growth of multiple myeloma and in the development of osteolytic lesions: a study in the 5TMM model.

Eline Menu, Evy De Leenheer, Hendrik De Raeve, Les Coulton, Takeshi Imanishi, Kazuyuki Miyashita, Els Van Valckenborgh, Ivan Van Riet, Ben Van Camp, Richard Horuk and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical & experimental metastasis, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

53 citing papers in PubMed, 114 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Immunocompetent Mouse Models of Multiple Myeloma: Therapeutic Implications.Hematology/oncology clinics of North America · 2024
    Review
  6. The Relationship ofJournal of clinical medicine · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Reduction of leukemic burden via bone-targeted nanoparticle delivery of an inhibitor of C-chemokine (C-C motif) ligand 3 (CCL3) signaling.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Multiple Myeloma and Bone: The Fatal Interaction.Cold Spring Harbor perspectives in medicine · 2018
    Review
  18. Review
  19. Review
  20. 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

12 authors at 4 institutions in 3 countries.

Eline MenuDepartment of Hematology and Immunology, Vrije Universiteit Brussel-VUB, Laarbeeklaan 103, 1090 Brussels, Belgium, Eline.Menu@vub.ac.be
Evy De Leenheer
Hendrik De Raeve
Les Coulton
Takeshi Imanishi
Kazuyuki Miyashita
Els Van Valckenborgh
Ivan Van Riet
Ben Van Camp
Richard Horuk
Peter Croucher
Karin Vanderkerken
Vrije Universiteit Brussel · BEUniversity of Sheffield · GBOsaka University · JPUniversity of Antwerp · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a plasma cell malignancy, characterized by the localization of the MM cells in the bone marrow (BM), where they proliferate and induce osteolysis. The MM cells first need to home or migrate to the BM to receive necessary survival signals. In this work, we studied the role of CCR1 and CCR5, two known chemokine receptors, in both chemotaxis and osteolysis in the experimental 5TMM mouse model. A CCR1-specific (BX471) and a CCR5-specific (TAK779) antagonist were used to identify the function of both receptors. We could detect by RT-PCR and flow cytometric analyses the expression of both CCR1 and CCR5 on the cells and their major ligand, macrophage inflammatory protein 1alpha (MIP1alpha) could be detected by ELISA. In vitro migration assays showed that MIP1alpha induced a 2-fold increase in migration of 5TMM cells, which could only be blocked by TAK779. In vivo homing kinetics showed a 30% inhibition in BM homing when 5TMM cells were pre-treated with TAK779. We found, in vitro, that both inhibitors were able to reduce osteoclastogenesis and osteoclastic resorption. In vivo end-term treatment of 5T2MM mice with BX471 resulted in a reduction of the osteolytic lesions by 40%; while TAK779 treatment led to a 20% decrease in lesions. Furthermore, assessment of the microvessel density demonstrated a role for both receptors in MM induced angiogenesis. These data demonstrate the differential role of CCR1 and CCR5 in MM chemotaxis and MM associated osteolysis and angiogenesis.

Indexed as

AmidesAnimalsBone MarrowBone ResorptionCCR5 Receptor AntagonistsCell DivisionCell Line, TumorCell MovementChemokine CCL3Chemokine CCL4Chemokines, CCChemotaxisFemaleMacrophage Inflammatory ProteinsMiceMice, Inbred C57BLAmidesBX 471Ccl3 protein, mouseCcr1 protein, mouseCCR5 Receptor AntagonistsChemokine CCL3Chemokine CCL4Chemokines, CCMacrophage Inflammatory ProteinsNeoplasm ProteinsPhenylurea CompoundsPiperidinesQuaternary Ammonium CompoundsReceptors, CCR1Receptors, CCR5Receptors, ChemokineRecombinant Fusion ProteinsTAK 779

Identifiers

PMID17086356
OpenAlexW2032434507

What OpenQuestion holds

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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.