Evidence map›Paper›PMID 41557613›Full record

ArticlePloS one2026

Prediction of myeloid malignant cells in Fanconi anemia using machine learning.

Luis A Flores-Mejía, Pablo Siliceo, Ulises Juárez Figueroa, Angel A De la Cruz, Cecilia Ayala-Zambrano, Hugo Tovar, Sara Frías, Alfredo Rodríguez

Abstract read
In one paragraph

Article in PloS one, 2026. 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
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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

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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

8 authors.

Luis A Flores-MejíaDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.
Pablo SiliceoDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.
Ulises Juárez FigueroaLaboratorio de Citogenética, Instituto Nacional de Pediatría, México.
Angel A De la CruzDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.
Cecilia Ayala-ZambranoDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.ORCID https://orcid.org/0009-0006-9823-6901
Hugo TovarComputational Genomics Division, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, Mexico.ORCID https://orcid.org/0000-0002-8360-6133
Sara FríasDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.ORCID https://orcid.org/0000-0002-3097-6368
Alfredo RodríguezDepartamento de Medicina Genómica y Toxicología Ambiental, Universidad Nacional Autónoma de México, México.ORCID https://orcid.org/0000-0002-1072-8631

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fanconi anemia (FA) is an inherited bone marrow failure syndrome with cancer predisposition. Most FA patients develop aplastic anemia during childhood and have an extremely high cumulative risk to develop cancer during their lifespan. Myeloid malignancy is one of the main neoplastic risks for patients with FA, including high-risk myelodysplastic syndrome (MDS), recently renamed as myelodysplastic neoplasm, and acute myeloid leukemia (AML). Although bone marrow transplantation is the treatment of choice for FA patients that develop aplastic anemia, patients with a more stable bone marrow remain not transplanted and at a high risk of presenting MDS/AML, these patients therefore should be monitored for appearance of myeloid malignant clones. Markers for an as-early-as-possible identification of emerging myeloid malignant cells are needed for the monitoring of patients with FA, since quick medical action after detection of neoplastic transformation is needed. In this work we have developed a deep neural network (DNN) model that was trained with publicly available single cell RNA-seq (scRNA-seq) datasets of patients with AML and used to predict the presence of AML-like cells in scRNA-seq datasets obtained from bone marrow samples of patients with FA. The predictor displayed high sensitivity, specificity, and accuracy for the detection of single-cell resolution myeloid malignant transcriptional profiles. Functional analyses of the predicted-AML cells from FA patients showed enrichment of lympho-myeloid-primed progenitor (LMPP) and granulocyte-monocyte progenitor (GMP) populations, as well as transcriptional profiles associated with malignant transformation. Cues of immune evasion were also detected using single cell pathway analysis (SCPA) and cell-cell communication profiles.

Indexed as

Fanconi AnemiaLeukemia, Myeloid, AcuteMachine LearningMyelodysplastic SyndromesHumansMyeloid CellsSingle-Cell Analysis

Identifiers

PMID41557613
PMCPMC12818649

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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.