Evidence map›Paper›PMID 30821712›Full record

ArticleJCI insight2019

Single-cell RNA sequencing of lung adenocarcinoma reveals heterogeneity of immune response-related genes.

Ke-Yue Ma, Alexandra A Schonnesen, Amy Brock, Carla Van Den Berg, S Gail Eckhardt, Zhihua Liu, Ning Jiang

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
5.1field-weighted citation impact, top 4% of its field
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

55 citing papers in PubMed, 79 citations in OpenAlex.

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  8. Single-Cell Informatics for Tumor Microenvironment and Immunotherapy.International journal of molecular sciences · 2024
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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

7 authors at 4 institutions in 3 countries.

Ke-Yue MaInstitute for Cellular and Molecular Biology, College of Natural Sciences.
Alexandra A SchonnesenDepartment of Biomedical Engineering, Cockrell School of Engineering, and.
Amy BrockInstitute for Cellular and Molecular Biology, College of Natural Sciences.
Carla Van Den BergInstitute for Cellular and Molecular Biology, College of Natural Sciences.
S Gail EckhardtDepartment of Oncology, LIVESTRONG Cancer Institutes, Dell Medical School, The University of Texas at Austin, Austin, Texas, USA.
Zhihua LiuDepartment of AnoRectal Surgery and.
Ning JiangInstitute for Cellular and Molecular Biology, College of Natural Sciences.
Institut de Biologie Moléculaire et Cellulaire · FRLivestrong Foundation · USAustin College · USGuangzhou Medical University · CN

Funding

Comprehensive Training Program in Imaging Science and InformaticsT32EB007507 · NIBIB · UNIVERSITY OF TEXAS AT AUSTIN · PI MARKEY, MIA K, RYLANDER, HENRY GRADY · 2009 to 2024
$2.7M
An integrated therapeutic T cell receptor screening platform for adoptive cell therapy in cancerR33CA225539 · NCI · UNIVERSITY OF TEXAS AT AUSTIN · PI JIANG, NING JENNY · 2018 to 2022
$1.1M
Genomic Approaches to the T Cell Receptor Repertoire during AgingR00AG040149 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI JIANG, NING JENNY · 2013 to 2015
$740k
NCI NIH HHS R33 CA225539NIA NIH HHS R00 AG040149NIBIB NIH HHS T32 EB007507
6 · The paper itself

Abstract

Immunotherapy has emerged as a promising approach to treat cancer. However, partial responses across multiple clinical trials support the significance of characterizing intertumor and intratumor heterogeneity to achieve better clinical results and as potential tools in selecting patients for different types of cancer immunotherapies. Yet, the type of heterogeneity that informs clinical outcome and patient selection has not been fully explored. In particular, the lack of characterization of immune response-related genes in cancer cells hinders the further development of metrics to select and optimize immunotherapy. Therefore, we analyzed single-cell RNA-Seq data from lung adenocarcinoma patients and cell lines to characterize the intratumor heterogeneity of immune response-related genes and demonstrated their potential impact on the efficacy of immunotherapy. We discovered that IFN-γ signaling pathway genes are heterogeneously expressed and coregulated with other genes in single cancer cells, including MHC class II (MHCII) genes. The downregulation of genes in IFN-γ signaling pathways in cell lines corresponds to an acquired resistance phenotype. Moreover, analysis of 2 groups of tumor-restricted antigens, namely neoantigens and cancer testis antigens, revealed heterogeneity in their expression in single cells. These analyses provide a rationale for applying multiantigen combinatorial therapies to prevent tumor escape and establish a basis for future development of prognostic metrics based on intratumor heterogeneity.

Indexed as

Adenocarcinoma of LungAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCell Line, TumorDatasets as TopicDown-RegulationExome SequencingFemaleGene Expression Regulation, NeoplasticGenes, MHC Class IIGenetic HeterogeneityHumansInterferon-gammaKaplan-Meier EstimateLung NeoplasmsMaleAntineoplastic Agents, ImmunologicalIFNG protein, humanInterferon-gammaBioinformaticsImmunologyImmunotherapyOncology

Identifiers

PMID30821712
PMCPMC6478414
OpenAlexW2917966987

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.