Evidence map›Paper›PMID 24340030›Full record

Trial reportPloS one2013

Bone marrow stromal cells derived MCP-1 reverses the inhibitory effects of multiple myeloma cells on osteoclastogenesis by upregulating the RANK expression.

Zhiqiang Liu, Jingda Xu, Haiyan Li, Yuhuan Zheng, Jin He, Huan Liu, Yuping Zhong, Yong Lu, Bangxing Hong, Mingjun Zhang and 7 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.3field-weighted citation impact, top 37% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Observational
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Ionizing Radiation Stimulates Expression of Pro-Osteoclastogenic Genes in Marrow and Skeletal Tissue.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2015
    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

17 authors at 4 institutions in 2 countries.

Zhiqiang LiuDepartment of Lymphoma and Myeloma, Division of Cancer Medicine, Center for Cancer Immunology Research, The University of Texas M D Anderson Cancer Center, Houston, Texas, United States of America.
Jingda Xu
Haiyan Li
Yuhuan Zheng
Jin He
Huan Liu
Yuping Zhong
Yong Lu
Bangxing Hong
Mingjun Zhang
Pei Lin
Juan Du
Jian Hou
Jianfei Qian
Larry W Kwak
Qing Yi
Jing Yang
The University of Texas MD Anderson Cancer Center · USCleveland Clinic Lerner College of Medicine · USCleveland Clinic · USSecond Military Medical University · CN

Funding

P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BERRY, DONALD A · 2010 to 2014
$11.1M
C-reactive protein promotes myeloma cell-mediated bone destructionR01CA138398 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2010 to 2014
$1.6M
Targeting surface b2M for myeloma and bone therapyR01CA138402 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2009 to 2013
$1.3M
Anti-beta2 microglobulin as a novel therapeutic agent in multiple myelomaR00CA137158 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YANG, JING · 2011 to 2013
$700k
Anti-beta2 microglobulin mAbs as a novel therapeutic agent in multiple myelomaK99CA137158 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YANG, JING · 2009 to 2010
$134k
NCI NIH HHS CA137158NCI NIH HHS CA138398NCI NIH HHS CA138402NCI NIH HHS K99 CA137158NCI NIH HHS P50 CA142509NCI NIH HHS R00 CA137158NCI NIH HHS R01 CA138398NCI NIH HHS R01 CA138402
6 · The paper itself

Abstract

Multiple myeloma (MM) cells are responsible for aberrant osteoclast (OC) activation. However, when cocultured monocytes, but not OC precursors, with MM cells, we made a novel observation that MM cells inhibited receptor activator of nuclear factor κB ligand (RANKL)-induced increase of OC differentiation, OC gene expression, signaling pathways and bone resorption activity. Our results showed that MM cells produced multiple inhibitory cytokines of osteoclastogenesis, such as IL-10, which activated STAT3 signaling and induce OC inhibition. However, cocultures of bone marrow stromal cells (BMSCs) reversed MM-induced OC inhibition. We found that MM cells increased production of MCP-1 from BMSCs and BMSC-derived MCP-1 enhanced OC formation. Mechanistic studies showed that IL-10 downregulated RANK expression in monocytes and thus, inhibited RANKL-induced OC formation. In contrast, MCP-1 upregulated RANK expression and thus, enhanced OC formation. Overall, our studies for the first time demonstrated that MM cell have inhibitory effects on osteoclastogenesis by producing inhibitory cytokines. Our results further indicate that activation of osteoclastogenesis in bone marrow requests the crosstalk of MM cells, BMSCs and their produced cytokines. Thus, our studies provide evidences that targeting bone marrow microenvironmental cells and/or cytokines may be a new approach to treating MM bone destruction.

Indexed as

Gene Expression Regulation, NeoplasticBone Marrow CellsChemokine CCL2Coculture TechniquesFemaleHumansInterleukin-10MaleMonocytesMultiple MyelomaNeoplasm ProteinsOsteoclastsReceptor Activator of Nuclear Factor-kappa BStromal CellsTumor Cells, CulturedUp-RegulationCCL2 protein, humanChemokine CCL2IL10 protein, humanInterleukin-10Neoplasm ProteinsReceptor Activator of Nuclear Factor-kappa BTNFRSF11A protein, human

Identifiers

PMID24340030
PMCPMC3858321
OpenAlexW2100542268

What OpenQuestion holds

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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.