Evidence map›Paper›PMID 30935386›Full record

ArticleJournal of translational medicine2019

High expression of miR-363 predicts poor prognosis and guides treatment selection in acute myeloid leukemia.

Huihui Zhang, Ninghan Zhang, Rong Wang, Tingting Shao, Yuan Feng, Yao Yao, Qingyun Wu, Shengyun Zhu, Jiang Cao, Huanxin Zhang and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 19% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Identification of Acute Myeloid Leukemia Bone Marrow Circulating MicroRNAs.International journal of molecular sciences · 2020
    Article
  8. Article
  9. 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

14 authors at 1 institution in 1 country.

Huihui ZhangBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Ninghan ZhangBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Rong WangBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Tingting ShaoBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Yuan FengBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Yao YaoBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Qingyun WuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Shengyun ZhuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Jiang CaoDepartment of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Huanxin ZhangDepartment of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zhenyu LiBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xuejiao LiuInsititute of Nervous System Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Mingshan NiuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. msniu24@126.com.ORCID 0000-0002-7077-6467
Kailin XuBlood Diseases Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China. lihmd@163.com.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute myeloid leukemia (AML) is a highly heterogeneous malignancy with various outcomes, and therefore needs better risk stratification tools to help select optimal therapeutic options.

methodsIn this study, we identify miRNAs that could predict clinical outcome in a heterogeneous AML population using TCGA dataset.

resultsWe found that MiR-363 is a novel prognostic factor in AML patients undergoing chemotherapy. In multivariable analyses, high miR-363 remained predictive for shorter OS (HR = 2.349, P = 0.012) and EFS (HR = 2.082, P = 0.001) independent of other well-known prognostic factors. More importantly, allogeneic hematopoietic stem cell transplantation (allo-HSCT) overcame the adverse outcomes related to high miR-363 expression. In gene expression profiling, high miR-363 expression was positively correlated with the amounts of leukemogenic transcription factors, including Myb, RUNX3, GATA3, IKZF3, ETS1 and MLLT3. Notably, we found that the in silico predicted target genes (EZH2, KLF6 and PTEN) of miR-363 were downregulated in association with high miR-363 expression.

conclusionsIn summary, miR-363 expression may help identify patients in need of strategies to select the optimal therapy between chemotherapeutic and allo-HCST regimens. AML patients with high miR-363 expression may be highly recommended for early allo-HSCT regimen.

Indexed as

Patient SelectionAdolescentAdultAgedAged, 80 and overAntineoplastic AgentsBiomarkers, TumorFemaleGene Expression Regulation, LeukemicHematopoietic Stem Cell TransplantationHumansLeukemia, Myeloid, AcuteMaleMicroRNAsMiddle AgedPredictive Value of TestsAntineoplastic AgentsBiomarkers, TumorMicroRNAsMIRN363 microRNA, humanAcute myeloid leukemiaAllo-HSCTChemotherapyClinical outcomeMir-363

Identifiers

PMID30935386
PMCPMC6444823
OpenAlexW2941198082

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LicenceCC BY
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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.