Evidence map›Paper›PMID 30123422›Full record

ArticleOncotarget2018

Impact of cell fusion in myeloma marrow microenvironment on tumor progression.

Ziyan Wang, Yuqing Yuan, Liying Zhang, Zhou Min, Dongming Zhou, Sun Yu, Panjun Wang, Songguang Ju, Li Jun, Jinxiang Fu

Abstract read
In one paragraph

Article in Oncotarget, 2018. 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
–field-weighted citation impact
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.

  1. Implications of Heterotypic Cell Fusion in Cancer.Advances in experimental medicine and biology · 2026
    Review
  2. Review
  3. Mechanisms of Cell Fusion in Cancer.Results and problems in cell differentiation · 2024
    Review
  4. Cell Fusion and Syncytia Formation in Cancer.Results and problems in cell differentiation · 2024
    Review
  5. Review
  6. Article
  7. Adult Stem Cell Functioning in the Tumor Micro-Environment.International journal of molecular sciences · 2019
    Review
  8. How cells fuse.The Journal of cell biology · 2019
    Review
  9. Tumor Microenvironment and Cell Fusion.BioMed research international · 2019
    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

10 authors.

Ziyan WangHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Yuqing YuanHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Liying ZhangHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Zhou MinHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Dongming ZhouHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Sun YuHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Panjun WangHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Songguang JuInstitute of Biotechnology, Soochow University, Suzhou 215007, PR China.
Li JunHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.
Jinxiang FuHematology Department, The Second Affiliated Hospital of Soochow University, Suzhou 215004, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) represent a subset of non-hematopoietic adult stem cells, which can also fuse with other cells spontaneously in bone marrow and capable of adopting the phenotype of other cells. The fusion of somatic cells with stem cells can reprogram somatic cells to a pluripotent state. Our research on the fusion of bone marrow mesenchymal stem cells(BM-MSCs) and MM cells demonstrate that the fused cells can exhibit stemness and cancer cell-like characteristics.

resultsWe successfully produced a hybrid cells that acquired larger size and multinucleation, in which partial chromatin condensation, a visible nucleolus, and one or more round or oval nucleus. Experiments results showed that the stemness markers highly expressed in these fused cells and there were much more chromosomes in fused cells than those in parental cells as well as exhibited increased resistance to drug treatment.

conclusionsOur results suggest that cell fusion between BM-MSCs and MM cells could contribute it genomic heterogeneity and play a role on disease progression.

methodsWe fused human BM-MSCs with MM cells lines RPMI 8226 or XG1

Indexed as

bone marrow microenvironmentcell fusionchemoresistancemesenchymal stem cellmultiple myeloma

Identifiers

PMID30123422
PMCPMC6089556

What OpenQuestion holds

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Registered trials

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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.