Evidence map›Paper›PMID 41473338›Full record

ReviewInternational journal of general medicine2025

Integrated Proteomic and Metabolomic Profiling in Acute Promyelocytic Leukemia: Current Status and Perspectives.

Ting Liu, Mengqi Qu, Ning Wang, Xue Xing

Abstract readReview
In one paragraph

Review in International journal of general medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Ting Liu *Department of Clinical Laboratory, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116021, People's Republic of China.
Mengqi Qu *Department of Clinical Laboratory, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116021, People's Republic of China.
Ning WangDepartment of Clinical Laboratory, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116021, People's Republic of China.
Xue XingDepartment of Clinical Laboratory, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116021, People's Republic of China.ORCID 0009-0003-4650-0684

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute promyelocytic leukemia(APL), a distinct subtype of acute myeloid leukemia(AML), has garnered significant attention in recent years regarding its pathogenesis and the molecular basis of its treatment response. With the rapid advancement of proteomics and metabolomics technologies, researchers can now delve deeper into revealing the molecular characteristics of acute promyelocytic leukemia and the regulatory role of its microenvironment. This review summarizes the latest research progress in proteomics and metabolomics within the acute promyelocytic leukemia field, focusing on analyzing the critical role of the the promyelocytic leukemia-retinoic acid receptor alpha (PML::RARα) fusion gene fusion protein in regulating cellular metabolism and protein expression. Furthermore, the article explores the importance of the immune system in acute promyelocytic leukemia treatment response and the impact of all-trans retinoic acid/arsenic trioxide therapy on the proteome and metabolome. By synthesizing existing research findings, this review aims to discuss how proteomic and metabolomic data elucidate the pathological mechanisms and therapeutic targets of acute promyelocytic leukemia, providing a theoretical basis for future precision medicine and translational research.

Indexed as

acute promyelocytic leukemiaimmunoregulationmetabolitesmetabolomicspml::rarα fusion proteinproteomicstreatment response

Identifiers

PMID41473338
PMCPMC12746738

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.