Evidence map›Paper›PMID 32165482›Full record

ArticleHaematologica2021

P2X7 promotes the progression of MLL-AF9 induced acute myeloid leukemia by upregulation of Pbx3.

Wenli Feng, Xiao Yang, Lina Wang, Rong Wang, Feifei Yang, Hao Wang, Xiaoli Liu, Qian Ren, Yingchi Zhang, Xiaofan Zhu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  12. Animal Models for the Investigation of P2X7 Receptors.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Spotlight on P2X7 Receptor PET Imaging: A Bright Target or a Failing Star?International journal of molecular sciences · 2023
    Review
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  18. Put in a "CaCells · 2022
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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

11 authors at 1 institution in 1 country.

Wenli FengInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Xiao YangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Lina WangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Rong WangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Feifei YangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Hao WangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Xiaoli LiuInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Qian RenInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Yingchi ZhangInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Xiaofan ZhuInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Guoguang ZhengInstitute of Hematology and Blood Diseases Hospital, Peking Union Medical College, China.
Institute of Hematology & Blood Diseases Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nucleotides mediate intercellular communication by activating purinergic receptors and take part in various physiological and pathological processes. Abnormal purinergic signaling plays important roles in malignant progression. P2X7, which belongs to the P2X family of purinergic receptors, is abnormally expressed in various types of malignancies including leukemia. However, its role and molecular mechanism in leukemia have not been elucidated. Here, we analyzed the correlation between P2X7 expression and AML clinical outcome; explored the role and mechanism of P2X7 in AML progression by using mouse acute myeloid leukemia (AML), nude mouse xenograft and patient-derived xenograft models. High levels of P2X7 expression were correlated with worse survival in AML. P2X7 was highly expressed in MLL-rearranged AML. Furthermore, P2X7 accelerated the progression of MLL-rearranged AML by both promoting cell proliferation and increasing leukemia stem cell (LSC) levels. Moreover, P2X7 caused upregulation of Pbx3 accounts for its pro-leukemic effects. The P2X7-Pbx3 pathway might also contribute to the progression of other types of leukemia as well as solid tumors with high levels of P2X7 expression. Our study provides new insights into the malignant progression caused by abnormal purinergic signaling.

Indexed as

Gene Expression Regulation, LeukemicLeukemia, Myeloid, AcuteOncogene Proteins, FusionReceptors, Purinergic P2X7AnimalsMiceMyeloid-Lymphoid Leukemia ProteinSignal TransductionTranscriptional ActivationUp-RegulationMLL-AF9 fusion protein, mouseMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionP2rx7 protein, mouseReceptors, Purinergic P2X7

Identifiers

PMID32165482
PMCPMC8094107
OpenAlexW3012149196

What OpenQuestion holds

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LicenceCC BY-NC
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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.