Evidence map›Paper›PMID 28978095›Full record

ArticleOncotarget2017

Melphalan modifies the bone microenvironment by enhancing osteoclast formation.

Ryan C Chai, Michelle M McDonald, Rachael L Terry, Nataša Kovačić, Jenny M Down, Jessica A Pettitt, Sindhu T Mohanty, Shruti Shah, Gholamreza Haffari, Jiake Xu and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Targeting NOTCH3 to eradicate dormant and therapy-resistant multiple myeloma cells.Journal of experimental & clinical cancer research : CR · 2026
    Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Osteoclast Multinucleation: Review of Current Literature.International journal of molecular sciences · 2020
    Review
  9. 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

15 authors at 7 institutions in 3 countries.

Ryan C ChaiBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Michelle M McDonaldBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Rachael L TerryBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Nataša KovačićBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Jenny M DownBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Jessica A PettittBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Sindhu T MohantyBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Shruti ShahBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Gholamreza HaffariFaculty of Information Technology, Monash University, Clayton, Australia.
Jiake XuSchool of Pathology and Laboratory Medicine, The University of Western Australia, Nedlands, Australia.
Matthew T GillespieFaculty of Medicine and Health Sciences, Monash University, Clayton, Australia.
Michael J RogersBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
John T PriceCollege of Health and Biomedicine, Victoria University, St Albans, Australia.
Peter I CroucherBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Julian M W QuinnBone Biology Division, Garvan Institute of Medical Research, Darlinghurst, Australia.
Garvan Institute of Medical Research · AUMonash University · AUUniversity of Melbourne · AUUniversity of Sheffield · GBUniversity of Western Australia · AUUniversity of Zagreb · HRUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melphalan is a cytotoxic chemotherapy used to treat patients with multiple myeloma (MM). Bone resorption by osteoclasts, by remodeling the bone surface, can reactivate dormant MM cells held in the endosteal niche to promote tumor development. Dormant MM cells can be reactivated after melphalan treatment; however, it is unclear whether melphalan treatment increases osteoclast formation to modify the endosteal niche. Melphalan treatment of mice for 14 days decreased bone volume and the endosteal bone surface, and this was associated with increases in osteoclast numbers. Bone marrow cells (BMC) from melphalan-treated mice formed more osteoclasts than BMCs from vehicle-treated mice, suggesting that osteoclast progenitors were increased. Melphalan also increased osteoclast formation in BMCs and RAW264.7 cells

Indexed as

bone lossbone microenvironmentcell stresschemotherapyosteoclast

Identifiers

PMID28978095
PMCPMC5620235
OpenAlexW2736303031

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.