Evidence map›Paper›PMID 42078544›Full record

ReviewFrontiers in pediatrics2026

Advances in multi-omics research on neuroblastoma.

Yubing Wang, Zhifei Zhao, Jinbin Wang, Shujie Song, Chengmin Zhao, Chao Qv, Hongting Lu

Abstract readReview
In one paragraph

Review in Frontiers in pediatrics, 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
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

7 authors.

Yubing Wang *Department of Pediatric Surgical Oncology, Affiliated Women and Children's Hospital of Qingdao University, Qingdao, Shandong, China.
Zhifei Zhao *Department of Pediatric Surgical Oncology, Affiliated Women and Children's Hospital of Qingdao University, Qingdao, Shandong, China.
Jinbin WangDepartment of Pediatric Surgical Oncology, Affiliated Women and Children's Hospital of Qingdao University, Qingdao, Shandong, China.
Shujie SongDepartment of Pediatric Surgical Oncology, Affiliated Women and Children's Hospital of Qingdao University, Qingdao, Shandong, China.
Chengmin ZhaoDepartment of Thoracic and Cardiovascular Surgery, Weifang Second People's Hospital, Weifang, Shandong, China.
Chao QvDepartment of Hepatobiliary and Pancreas, Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Hongting LuDepartment of Pediatric Surgical Oncology, Affiliated Women and Children's Hospital of Qingdao University, Qingdao, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroblastoma is the most common extracranial solid tumor in children, presenting significant challenges in diagnosis and treatment due to its highly heterogeneous clinical manifestations and complex genetic background. In recent years, advances in transcriptomics have played a pivotal role in this field, not only aiding in the identification of molecular subtypes of tumors but also revealing potential mechanisms of drug resistance. Through comprehensive gene expression profiling and single-cell sequencing technology, researchers have deeply analyzed key interaction nodes within the metabolic-immune microenvironment, providing a theoretical basis for developing targeted therapeutic strategies. Concurrently, radiomics, leveraging imaging techniques such as MRI, PET-CT, and CT, quantitatively assesses the morphological and metabolic characteristics of tumors. This enables non-invasive prediction of MYCN amplification status, evaluation of bone marrow metastasis risk, and prognostic stratification, thereby supporting dynamic disease monitoring. In pathology, artificial intelligence technology is widely applied in the analysis of digital pathology images. It effectively identifies cellular diversity and immune microenvironment features in tissues, enhancing diagnostic accuracy and assisting in predicting potential gene mutations. More importantly, integrating transcriptomics, radiology, and pathology data through multi-omics approaches overcomes the limitations of single data types. This integration constructs more precise disease classification models and facilitates the development of personalized treatment plans. This review emphasizes the critical roles of transcriptomics, radiomics, digital pathology analysis, and multi-omics fusion strategies in enhancing diagnostic precision for neuroblastoma and optimizing treatment decisions.

Indexed as

multi-omics integrationneuroblastomapathomicsradiomicstranscriptomics

Identifiers

PMID42078544
PMCPMC13128637

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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.