Evidence map›Paper›PMID 35003079›Full record

ArticleFrontiers in immunology2021

m6A Modification Patterns With Distinct Immunity, Metabolism, and Stemness Characteristics in Soft Tissue Sarcoma.

Zhen-Dong Huang, Lu-Lu Lin, Zi-Zhen Liu, Chao Hu, Hui-Yun Gu, Ren-Xiong Wei

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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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.

Zhen-Dong HuangDepartment of Spine and Orthopedic Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Lu-Lu LinDepartment of Pathology and Pathophysiology, School of Basic Medicine, Wuhan University, Wuhan, China.
Zi-Zhen LiuThe Third Clinical School, Hubei University of Medicine, Shiyan, China.
Chao HuDepartment of Spine and Orthopedic Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Hui-Yun GuDepartment of Spine and Orthopedic Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Ren-Xiong WeiDepartment of Spine and Orthopedic Oncology, Zhongnan Hospital of Wuhan University, Wuhan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

N6-methyladenosine (m6A) RNA methylation has been shown to have prognostic value in cancer. Nonetheless, its potential role regarding immunity, metabolism, and stemness in soft tissue sarcoma (STS) remains unknown. We comprehensively estimated the m6A modification patterns and corresponding immunity, metabolism, and stemness characteristics based on 568 STS samples and 21 m6A regulators. The m6Ascore was constructed to quantify m6A modification patterns in individuals using machine learning algorithms. Two distinct m6A modification patterns among the STS patients were identified, which exhibited differences in prognosis, immune cell infiltration, metabolic pathways, stemness, somatic mutation, and copy number variation. Thereafter, immunity-, metabolism-, and stemness phenotype-related genes associated with m6A modification were identified. Furthermore, patients with lower m6Ascores had increased antitumor immune responses, survival benefit under immunotherapy, tumor mutation burden, immunogenicity, and response to anti-PD-1/L1 immunotherapy. Immunotherapy sensitivity was validated using the IMvigor210 dataset. STS patients with lower m6Ascore might be more sensitive to docetaxel and gemcitabine. Finally, pan-cancer analysis illustrated the significant correlations of m6Ascore with clinical outcomes, immune cell infiltration, metabolism, and stemness. This study revealed that m6A modification plays an important role in immunity, metabolism, and stemness in STS. Evaluating the m6A modification pattern and development of m6Ascore may help to guide more effective immunotherapy and chemotherapy strategies.

Indexed as

AdenosineAntineoplastic AgentsDeoxycytidineDNA Copy Number VariationsDNA MethylationDocetaxelGemcitabineGene Expression Regulation, NeoplasticHumansImmunotherapyKaplan-Meier EstimateSarcomaAdenosineAntineoplastic AgentsDeoxycytidineDocetaxelGemcitabineN-methyladenosinecancer molecular subtypesimmunotherapym6A methylationsoft tissue sarcomatumor microenvironment

Identifiers

PMID35003079
PMCPMC8739240

What Socratic 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 Socratic graph.