Evidence map›Paper›PMID 35802677›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2022

DNA Methylation Profiling Identifies Subgroups of Lung Adenocarcinoma with Distinct Immune Cell Composition, DNA Methylation Age, and Clinical Outcome.

Kayla Guidry, Varshini Vasudevaraja, Kristen Labbe, Hussein Mohamed, Jonathan Serrano, Brett W Guidry, Michael DeLorenzo, Hua Zhang, Jiehui Deng, Soumyadip Sahu and 7 more

Abstract read
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In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

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  17. A novel subtype based on driver methylation-transcription in lung adenocarcinoma.Journal of cancer research and clinical oncology · 2024
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Kayla GuidryLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0001-8190-0278
Varshini VasudevarajaDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0001-9678-6375
Kristen LabbeLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0001-6731-5849
Hussein MohamedDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0001-7489-122X
Jonathan SerranoDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0002-2839-9573
Brett W GuidrySacred Heart University, Fairfield, Connecticut.ORCID 0000-0002-2679-3710
Michael DeLorenzoDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0001-6722-0890
Hua ZhangLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.
Jiehui DengLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0001-7986-8643
Soumyadip SahuLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0002-2497-864X
Christina AlmonteLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0003-3008-1342
Andre L MoreiraDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0003-1857-3774
Aristotelis TsirigosDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0002-7512-8477
Thales PapagiannakopoulosLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0002-2251-1624
Harvey PassDepartment of Cardiothoracic Surgery, New York University Langone Medical Center, New York, New York.ORCID 0000-0003-3222-3471
Matija SnuderlDepartment of Pathology, New York University School of Medicine, New York, New York.ORCID 0000-0003-0752-0917
Kwok-Kin WongLaura and Isaac Perlmutter Cancer Center, New York University Langone Medical Center, New York, New York.ORCID 0000-0001-6323-235X

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANIRBAN MAITRA · 1985 to 2026
$83.1M
The EDRN Mesothelioma Biomarker Discovery LaboratoryU01CA214195 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI PASS, HARVEY IRA, YANG, HAINING · 2016 to 2021
$3.5M
Multispectral imaging & analysis of intact tissue sections w/ the Perkin Elmer VectraS10OD021747 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LOOMIS, CYNTHIA A · 2016 to 2016
$359k
NCI NIH HHS P30 CA016087NCI NIH HHS U01 CA214195NIH HHS S10 OD021747
6 · The paper itself

Abstract

purposeLung adenocarcinoma (LUAD) is a clinically heterogeneous disease, which is highlighted by the unpredictable recurrence in low-stage tumors and highly variable responses observed in patients treated with immunotherapies, which cannot be explained by mutational profiles. DNA methylation-based classification and understanding of microenviromental heterogeneity may allow stratification into clinically relevant molecular subtypes of LUADs. EXPERIMENTAL

designWe characterize the genome-wide DNA methylation landscape of 88 resected LUAD tumors. Exome sequencing focusing on a panel of cancer-related genes was used to genotype these adenocarcinoma samples. Bioinformatic and statistical tools, the immune cell composition, DNA methylation age (DNAm age), and DNA methylation clustering were used to identify clinically relevant subgroups.

resultsDeconvolution of DNA methylation data identified immunologically hot and cold subsets of LUADs. In addition, concurrent factors were analyzed that could affect the immune microenvironment, such as smoking history, ethnicity, or presence of KRAS or TP53 mutations. When the DNAm age was calculated, a lower DNAm age was correlated with the presence of a set of oncogenic drivers, poor overall survival, and specific immune cell populations. Unsupervised DNA methylation clustering identified six molecular subgroups of LUAD tumors with distinct clinical and microenvironmental characteristics.

conclusionsOur results demonstrate that DNA methylation signatures can stratify LUAD into clinically relevant subtypes, and thus such classification of LUAD at the time of resection may lead to better methods in predicting tumor recurrence and therapy responses.

Indexed as

AdenocarcinomaAdenocarcinoma of LungLung NeoplasmsDNA MethylationHumansMutationTumor Microenvironment

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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.