Evidence map›Paper›PMID 29493383›Full record

ArticleUpsala journal of medical sciences2018

MiR-130a is aberrantly overexpressed in adult acute myeloid leukemia with t(8;21) and its suppression induces AML cell death.

Chao Ding, Su-Ning Chen, Roderick A F Macleod, Hans G Drexler, Stefan Nagel, De-Pei Wu, Ai-Ning Sun, Hai-Ping Dai

Open access · diamondAbstract read
In one paragraph

Article in Upsala journal of medical sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 23% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Targeting microRNA in hematologic malignancies.Current opinion in oncology · 2020
    Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. MicroRNAs as prognostic biomarker and relapse indicator in leukemia.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2017
    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

8 authors at 2 institutions in 2 countries.

Chao Dinga Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University , Suzhou , People's Republic of China.
Su-Ning Chena Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University , Suzhou , People's Republic of China.
Roderick A F Macleodc Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures , Braunschweig , Germany.
Hans G Drexlerc Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures , Braunschweig , Germany.
Stefan Nagelc Leibniz Institute DSMZ-German Collection of Microorganisms and Cell Cultures , Braunschweig , Germany.
De-Pei Wua Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University , Suzhou , People's Republic of China.
Ai-Ning Suna Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University , Suzhou , People's Republic of China.
Hai-Ping Daia Jiangsu Institute of Hematology, The First Affiliated Hospital of Soochow University , Suzhou , People's Republic of China.ORCID http://orcid.org/0000-0003-1125-7744
Soochow University · CNLeibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmerging evidence has revealed that miRNAs can function as oncogenes or tumor suppressor genes in leukemia. The ectopic expression of miR-130a has been reported in chronic leukemia, but our understanding of the biological implications of miR-130a expression remains incomplete.

methodsWe quantified a cohort of de novo acute myeloid leukemia (AML) by bead-based miRNA and real-time quantitative PCR (Rq-PCR). The luciferase reporter gene assay was analyzed after the plasmid constructs which contain 5'-UTR of miR-130a and a Renilla luciferase reporter plasmid were transfected simultaneously into 293T cells. MTT and caspase 3/7 apoptosis assays were used to test cell viability and apoptosis.

resultsWe identified miR-130a as significantly overexpressed in t(8;21) AML. Expression of miR-130a decreased significantly once patients with t(8;21) achieved complete remission, but increased sharply at the time of relapse. In patients with t(8;21) AML, KIT mutational status was associated with miR-130a expression-with higher expression associated with KIT activating mutations. Increased miR-130a expression in t(8;21) AML was associated with slightly worse event-free survival; however, no impact on overall survival was observed. Knockdown of AML1/ETO protein in the SKNO-1 cell line resulted in decrease of expression of miR-130a. Direct binding of AML1/ETO fusion protein with the promoter sequence of miR-130a was detected with luciferase reporter gene assay. Following miR-130a knockdown, SKNO-1 demonstrated increased sensitivity to etoposide.

conclusionsOur data suggest that miR-130a is directly activated by AML1/ETO, and may act as a factor which is associated with leukemia burden, event-free survival, and chemotherapy sensitivity in t(8;21) AML.

Indexed as

ApoptosisChromosomes, Human, Pair 21Chromosomes, Human, Pair 8Translocation, GeneticAdultCell Line, TumorCore Binding Factor Alpha 2 SubunitEtoposideFemaleHumansLeukemia, Myeloid, AcuteMaleMicroRNAsOncogene Proteins, FusionRUNX1 Translocation Partner 1 ProteinAML1-ETO fusion protein, humanCore Binding Factor Alpha 2 SubunitEtoposideMicroRNAsMIRN130 microRNA, humanOncogene Proteins, FusionRUNX1 Translocation Partner 1 ProteinAcute myeloid leukemiamiR-130aoutcomeoverexpressiont(8;21)

Identifiers

PMID29493383
PMCPMC5901465
OpenAlexW2794321299

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.