Evidence map›Paper›PMID 26689580›Full record

ArticlePathology oncology research : POR2016

Study on the Association Between miRNA-202 Expression and Drug Sensitivity in Multiple Myeloma Cells.

Xianjuan Shen, Yuehua Guo, Jing Qi, Wei Shi, Xinhua Wu, Hongbing Ni, Shaoqing Ju

Abstract read
PubMed Publisher
In one paragraph

Article in Pathology oncology research : POR, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. The microRNA-202 as a Diagnostic Biomarker and a Potential Tumor Suppressor.International journal of molecular sciences · 2022
    Review
  6. Review
  7. Review
  8. Liquid biopsies for multiple myeloma in a time of precision medicine.Journal of molecular medicine (Berlin, Germany) · 2020
    Review
  9. Article
  10. Emerging targets in cancer drug resistance.Cancer drug resistance (Alhambra, Calif.) · 2019
    Review
  11. MiR-202-5p/Cancer biology & therapy · 2019
    Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. 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

7 authors at 2 institutions in 1 country.

Xianjuan ShenSurgical Comprehensive Laboratory, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Yuehua GuoNantong University, #9 Seyuan Road, Nantong, 226001, JS, People's Republic of China.
Jing QiSurgical Comprehensive Laboratory, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Wei ShiSurgical Comprehensive Laboratory, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Xinhua WuSurgical Comprehensive Laboratory, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Hongbing NiLaboratory Medicine Center, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China.
Shaoqing JuSurgical Comprehensive Laboratory, Affiliated Hospital of Nantong University, #20 Xisi Road, Nantong, 226001, JS, People's Republic of China. jsq814@hotmail.com.
Nantong University · CNAffiliated Hospital of Nantong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing amount of experimental evidence has shown that miRNAs play a causal role in hematologic tumorigenesis. In this study, we characterized the role of miR-202 in multiple myeloma (MM) drug sensitivity. The potential binding site of miR-202 and B cell-activating factor (BAFF) was confirmed by luciferase reporter assay. MM cells were transfected with miR-202 mimics and inhibitor. Cells growth was measured by WST-1 cell proliferation assay and Annexin V-FLUOS apoptosis assay. BAFF and miR-202 mRNA levels were measured by real-time PCR. Meanwhile, BAFF, Bcl-2 family survival proteins and MAPK pathway proteins were measured by Western blot. It was found that miR-202 was functioned as a modulator of BAFF expression. miR-202 over-expression sensitized MM cells to bortezomib (Bort) but less to Thalidomide (Thal) and dexamethasone (Dex). miR-202 mimics in combination with Bort inhibited MM cell survival more effectively as compared with Bort treatment alone. Our study also provided experimental evidence that JNK/SAPK signaling pathway was involved in the regulatory effect of miR-202 on drug resistance of MM cells. These results suggest that the regulatory mechanism of miR-202 expression may be a promising target for fine-tuning anti-myeloma therapy.

Indexed as

AgedApoptosisApoptosis Regulatory ProteinsB-Cell Activating FactorCell Line, TumorCell ProliferationDexamethasoneDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansMaleMAP Kinase Kinase 4MicroRNAsMiddle AgedMitogen-Activated Protein KinasesApoptosis Regulatory ProteinsB-Cell Activating FactorDexamethasoneMAP Kinase Kinase 4MicroRNAsMitogen-Activated Protein KinasesProto-Oncogene Proteins c-bcl-2RNA, MessengerThalidomideTNFSF13B protein, humanB cell-activating factor (BAFF)Drug resistancemicroRNAMultiple myeloma (MM)Signaling pathway

Identifiers

PMID26689580
OpenAlexW2276389344

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.