Evidence map›Paper›PMID 33077697›Full record

ArticleAging2020

MicroRNA-143 sensitizes acute myeloid leukemia cells to cytarabine via targeting ATG7- and ATG2B-dependent autophagy.

Hao Zhang, Jianmin Kang, Ling Liu, Lulu Chen, Saisai Ren, Yanling Tao

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
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  6. Review
  7. MircoRNAs predict and modulate responses to chemotherapy in leukemic patients.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Review
  8. Review
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  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. The dual role of autophagy in acute myeloid leukemia.Journal of hematology & oncology · 2022
    Review
  19. Article
  20. The regulatory roles of circular RNAsFrontiers in neurology · 2022
    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

6 authors at 2 institutions in 1 country.

Hao ZhangDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining 272029, Shandong Province, China.
Jianmin KangDepartment of Hematology, The Second Hospital of Shanxi Medical University, Taiyuan 030001, China.
Ling LiuDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining 272029, Shandong Province, China.
Lulu ChenGraduate School, Jining Medical University, Jining 272000, Shandong Province, China.
Saisai RenDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining 272029, Shandong Province, China.
Yanling TaoDepartment of Pediatric Hematology, Affiliated Hospital of Jining Medical University, Jining 272029, Shandong Province, China.
Affiliated Hospital of Jining Medical University · CNShanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting autophagy holds promise to enhance chemosensitivity in acute myeloid leukemia (AML). MicroRNA-143 (miR-143) has been found to suppress autophagy, however, it is not clear whether miR-143 augments cytarabine cytotoxicity in AML. Here, we report that cytarabine treatment reduces miR-143 expression in AML cell lines and primary AML cells. Moreover, ectopic expression of miR-143 further decreases cell viability in cytarabine-treated AML cells. By contrast, miR-143 knockdown inhibits cytarabine-induced cytotoxicity, together indicating a role of miR-143 in enhancing cytarabine sensitivity in AML. Subsequently, we show that miR-143 inhibits autophagy in cytarabine-treated AML cells by directly targeting autophagy-related proteins (ATG), ATG7 and ATG2B, two critical known components of autophagic machinery. More importantly, autophagy reconstructed via co-expression of ATG7 and ATG2B substantially attenuates miR-143-enhanced cytotoxicity, which is associated with suppression of caspase-dependent apoptotic pathway. Overall, this study demonstrates that targeting ATG7 and ATG2B-dependent autophagy is a critical mechanism by which miR-143 sensitizes AML to cytarabine, implicating it as a potential therapeutic target in AML treatment.

Indexed as

Antimetabolites, AntineoplasticApoptosisAutophagyAutophagy-Related Protein 7Autophagy-Related ProteinsCaspase 3Caspase 9CytarabineDose-Response Relationship, DrugGene Expression Regulation, LeukemicHL-60 CellsHumansLeukemia, Myeloid, AcuteMicroRNAsSignal TransductionU937 CellsAntimetabolites, AntineoplasticATG2B protein, humanATG7 protein, humanAutophagy-Related Protein 7Autophagy-Related ProteinsCASP3 protein, humanCASP9 protein, humanCaspase 3Caspase 9CytarabineMicroRNAsMIRN143 microRNA, humanVesicular Transport Proteinsacute myeloid leukemiaATG7autophagycytarabinemicroRNA-143

Identifiers

PMID33077697
PMCPMC7655171
OpenAlexW3092915417

What OpenQuestion holds

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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.