Evidence map›Paper›PMID 32381040›Full record

ArticleGenome biology2020

A human lung tumor microenvironment interactome identifies clinically relevant cell-type cross-talk.

Andrew J Gentles, Angela Bik-Yu Hui, Weiguo Feng, Armon Azizi, Ramesh V Nair, Gina Bouchard, David A Knowles, Alice Yu, Youngtae Jeong, Alborz Bejnood and 10 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  10. High-resolution transcriptomics analysis of CXCL13Journal of thoracic disease · 2024
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  16. International journal of molecular sciences · 2022
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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

20 authors at 7 institutions in 2 countries.

Andrew J GentlesDepartment of Medicine (Biomedical Informatics Research), Stanford University, Stanford, CA, 94035, USA. andrewg@stanford.edu.
Angela Bik-Yu HuiCancer Institute, Stanford University, Stanford, CA, 94035, USA.
Weiguo FengTranslational Medicine Group, Abbvie, North Chicago, IL, 60064, USA.
Armon AziziDepartment of Medicine (Biomedical Informatics Research), Stanford University, Stanford, CA, 94035, USA.
Ramesh V NairStanford Center for Genomics and Personalized Medicine, Stanford, USA.
Gina BouchardDepartment of Radiology, Stanford University, Stanford, USA.
David A KnowlesDepartment of Radiology, Stanford University, Stanford, USA.
Alice YuDepartment of Medicine (Biomedical Informatics Research), Stanford University, Stanford, CA, 94035, USA.
Youngtae JeongCancer Institute, Stanford University, Stanford, CA, 94035, USA.
Alborz BejnoodDepartment of Radiology, Stanford University, Stanford, USA.
Erna ForgóDepartment of Pathology, Stanford University, Stanford, USA.
Sushama VarmaDepartment of Pathology, Stanford University, Stanford, USA.
Yue XuDepartment of Thoracic Surgery, Stanford University, Stanford, USA.
Amanda KuongDepartment of Gynecology Oncology, CAP/Stanford Health Care Tri-Valley Outreach, Pleasanton, CA, USA.
Viswam S NairDivision of Pulmonary & Critical Care, Stanford University, Stanford, USA.
Rob WestDepartment of Pathology, Stanford University, Stanford, USA.
Matt van de RijnDepartment of Pathology, Stanford University, Stanford, USA.
Chuong D HoangThoracic and Oncologic Surgery Branch, CCR, NIH - National Cancer Institute, Bethesda, MD, USA.
Maximilian DiehnCancer Institute, Stanford University, Stanford, CA, 94035, USA. diehn@stanford.edu.
Sylvia K PlevritisDepartment of Biomedical Data Science, Stanford University, Stanford, CA, 94035, USA. plevriti@stanford.edu.
Stanford University · USAbbVie (United States) · USBroad Institute · USColumbia University · USNational Cancer Institute · USStanford Health Care · USStanford Medicine · US

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
Stanford Center for Clinical & Translational Education and Research (Spectrum)UL1TR003142 · NCATS · STANFORD UNIVERSITY · PI O'HARA, RUTH M · 2019 to 2023
$45.0M
Spectrum Stanford Center for clinical and Translational Research and EducationUL1TR001085 · NCATS · STANFORD UNIVERSITY · PI CULLEN, MARK RICHARD, GREENBERG, HARRY BERNARD · 2013 to 2017
$37.1M
Stanford Cancer Immune Monitoring and Analysis Center (CIMAC)U24CA224309 · NCI · STANFORD UNIVERSITY · PI Sean Curtis Bendall, Holden T. Maecker · 2017 to 2026
$19.9M
Spatial-Genomic Integrative Multi-Species Analysis of Lymph Node MetastasisU54CA209971 · NCI · STANFORD UNIVERSITY · PI NOLAN, GARRY P, PLEVRITIS, SYLVIA KATINA · 2016 to 2021
$11.0M
Clinically-Relevant Regulatory Networks in the Lung Tumor MicroenvironmentU01CA154969 · NCI · STANFORD UNIVERSITY · PI CLARKE, MICHAEL, PLEVRITIS, SYLVIA KATINA · 2011 to 2015
$2.8M
NCATS NIH HHS UL1 TR001085NCATS NIH HHS UL1 TR003142NCI NIH HHS U01CA154969NCI NIH HHS U24 CA224309NCI NIH HHS U54 CA209971
6 · The paper itself

Abstract

backgroundTumors comprise a complex microenvironment of interacting malignant and stromal cell types. Much of our understanding of the tumor microenvironment comes from in vitro studies isolating the interactions between malignant cells and a single stromal cell type, often along a single pathway.

resultTo develop a deeper understanding of the interactions between cells within human lung tumors, we perform RNA-seq profiling of flow-sorted malignant cells, endothelial cells, immune cells, fibroblasts, and bulk cells from freshly resected human primary non-small-cell lung tumors. We map the cell-specific differential expression of prognostically associated secreted factors and cell surface genes, and computationally reconstruct cross-talk between these cell types to generate a novel resource called the Lung Tumor Microenvironment Interactome (LTMI). Using this resource, we identify and validate a prognostically unfavorable influence of Gremlin-1 production by fibroblasts on proliferation of malignant lung adenocarcinoma cells. We also find a prognostically favorable association between infiltration of mast cells and less aggressive tumor cell behavior.

conclusionThese results illustrate the utility of the LTMI as a resource for generating hypotheses concerning tumor-microenvironment interactions that may have prognostic and therapeutic relevance.

Indexed as

Cell CommunicationReceptor Cross-TalkTumor MicroenvironmentAdenocarcinomaCarcinoma, Non-Small-Cell LungCell Line, TumorFibroblastsHumansIntercellular Signaling Peptides and ProteinsLung NeoplasmsPrimary Cell CultureGREM1 protein, humanIntercellular Signaling Peptides and Proteins

Identifiers

PMID32381040
PMCPMC7206807
OpenAlexW3023051088

What OpenQuestion holds

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LicenceCC BY
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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.