Evidence map›Paper›PMID 34006845›Full record

ArticleCell death & disease2021

LncRNA CD27-AS1 promotes acute myeloid leukemia progression through the miR-224-5p/PBX3 signaling circuit.

Yanling Tao, Jingjing Zhang, Lulu Chen, Xin Liu, Mingkang Yao, Hao Zhang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  4. LncRNAiScience · 2025
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  7. Article
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  13. Therapeutic potential ofFrontiers in pharmacology · 2023
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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

6 authors at 1 institution in 1 country.

Yanling TaoDepartment of Pediatric Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Jingjing ZhangDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Lulu ChenDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Xin LiuDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Mingkang YaoDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China.
Hao ZhangDepartment of Hematology, Affiliated Hospital of Jining Medical University, Jining, Shandong Province, China. zhanghaojyfy@126.com.ORCID 0000-0002-1925-6618
Affiliated Hospital of Jining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a hematological malignancy with a low cure rate, especially in the elderly. Previous studies have shown that long non-coding RNA (lncRNA) may be an important factor in the pathogenesis of hematological malignancies, including acute myeloid leukemia (AML). However, the biological roles and clinical significances of most lncRNAs in AML are not fully understood. LncRNA CD27 Antisense RNA 1 (CD27-AS1), as a member of lncRNA family, has rare reports on its function. In present study, we found that the expression of CD27-AS1 examined by quantitative real-time PCR was markedly increased in the AML patients (N = 40) compared with healthy volunteers (N = 40). The overall survival time was significantly shorter in patients with higher CD27-AS1 expression than that in patients with lower CD27-AS1 (P < 0.01). Furthermore, downregulation of CD27-AS1 in AML cells suppressed proliferative ability, arrested cell cycle in G0/G1 phase, and induced apoptosis. However, CD27-AS1 overexpression further enhanced the malignant phenotype of AML cells. Additionally, CD27-AS1 was proved to increase PBX3 expression through sponging miR-224-5p. CD27-AS1 knockdown blocked the MAPK signaling through PBX3 silencing and further inhibited the cell growth of AML cells. Taken together, we demonstrate that CD27-AS1 may be a potential prognostic biomarker of AML, and our finding also provides a new insight for non-coding RNA-based therapeutic intervention of AML.

Indexed as

Cell ProliferationDisease ProgressionHomeodomain ProteinsHumansLeukemia, Myeloid, AcuteMicroRNAsProto-Oncogene ProteinsRNA, AntisenseRNA, Long NoncodingTumor Necrosis Factor Receptor Superfamily, Member 7Homeodomain ProteinsMicroRNAsMIRN224 microRNA, humanproto-oncogene protein Pbx3Proto-Oncogene ProteinsRNA, AntisenseRNA, Long NoncodingTumor Necrosis Factor Receptor Superfamily, Member 7

Identifiers

PMID34006845
PMCPMC8131722
OpenAlexW3161975265

What OpenQuestion holds

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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.