Evidence map›Paper›PMID 27992381›Full record

ArticleOncotarget2017

Low-dose bortezomib increases the expression of NKG2D and DNAM-1 ligands and enhances induced NK and γδ T cell-mediated lysis in multiple myeloma.

Chao Niu, Haofan Jin, Min Li, Shan Zhu, Lei Zhou, Feng Jin, Yulai Zhou, Dongsheng Xu, Jianting Xu, Lianjing Zhao and 3 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 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

51 citing papers in PubMed, 72 citations in OpenAlex.

  1. Review
  2. Article
  3. T Cells Dysfunction in Multiple Myeloma.ImmunoTargets and therapy · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. CD4Journal of cancer research and clinical oncology · 2023
    Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
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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

13 authors at 3 institutions in 1 country.

Chao NiuCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Haofan JinCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Min LiCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Shan ZhuInstitute of Translational Medicine, The First Hospital of Jilin University, Changchun 130021, China.
Lei ZhouCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Feng JinCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Yulai ZhouCollege of Pharmacy, Jilin University, Changchun 130021, China.
Dongsheng XuCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Jianting XuCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Lianjing ZhaoCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Shanshan HaoCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Wei LiCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Jiuwei CuiCancer Center, The First Hospital of Jilin University, Changchun 130021, China.
Jilin University · CNFirst Hospital of Jilin University · CNTaian City Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is an incurable hematological malignancy, although bortezomib has markedly improved its outcomes. Growing clinical evidence indicates that enhancing induced natural killer (NK) or γδ T cells for infusion is useful in the treatment of MM. However, whether combination treatment with bortezomib and induced NK and γδ T cells further improves outcomes in MM, and how the treatments should be combined, remain unclear. Herein, we found that low-dose bortezomib did not suppress the viability of induced NK and γδ T cells, but did induce MM cell apoptosis. Importantly, low-dose bortezomib increased the expression of NKG2D and DNAM-1 ligands on MM cells, which sensitized the multiple myeloma cells to lysis by induced NK and γδ T cells. Our results suggested that combination treatment with low-dose bortezomib and induced NK or γδ T cells had a synergistic cytotoxic effect on MM cells. This study provided a proof of principle for the design of future trials and investigation of this combination therapeutic strategy for MM treatment.

Indexed as

AgedAntigens, Differentiation, T-LymphocyteAntineoplastic AgentsBortezomibCell Line, TumorCell SurvivalCombined Modality TherapyDose-Response Relationship, DrugFemaleGene Expression Regulation, NeoplasticHumansIntraepithelial LymphocytesKiller Cells, NaturalLigandsLymphocyte ActivationMaleAntigens, Differentiation, T-LymphocyteAntineoplastic AgentsBortezomibKLRK1 protein, humanLigandsNK Cell Lectin-Like Receptor Subfamily KT Lineage-Specific Activation Antigen 1bortezomibgamma-delta T cellsmultiple myelomanatural killer cells

Identifiers

PMID27992381
PMCPMC5351604
OpenAlexW2567460307

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.