Evidence map›Paper›PMID 36419822›Full record

ArticleCell genomics2022

Spatial intra-tumor heterogeneity is associated with survival of lung adenocarcinoma patients.

Hua-Jun Wu, Daniel Temko, Zoltan Maliga, Andre L Moreira, Emi Sei, Darlan Conterno Minussi, Jamie Dean, Charlotte Lee, Qiong Xu, Guillaume Hochart and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cell genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.4field-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

36 citing papers in PubMed, 47 citations in OpenAlex.

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  19. Spatial Architecture of Single-Cell and Vasculature in Tumor Microenvironment Predicts Clinical Outcomes in Triple-Negative Breast Cancer.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2025
    Article
  20. Unraveling Spatial Heterogeneity in Mass Spectrometry Imaging Data with GraphMSI.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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

18 authors at 8 institutions in 2 countries.

Hua-Jun WuCenter for Precision Medicine Multi-Omics Research, School of Basic Medical Sciences, Peking University Health Science Center and Peking University Cancer Hospital and Institute, Beijing, China.
Daniel TemkoDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Zoltan MaligaLaboratory of Systems Pharmacology and Department of Systems Biology, Harvard Medical School, Boston, MA 02215, USA.
Andre L MoreiraDepartment of Pathology, New York University Langone Health, New York, NY 10016, USA.
Emi SeiDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Darlan Conterno MinussiDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jamie DeanDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Charlotte LeeDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Qiong XuDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Guillaume HochartImaBiotech SAS, 59120 Loos, France.
Connor A JacobsonLaboratory of Systems Pharmacology and Department of Systems Biology, Harvard Medical School, Boston, MA 02215, USA.
Clarence YappLaboratory of Systems Pharmacology and Department of Systems Biology, Harvard Medical School, Boston, MA 02215, USA.
Denis SchapiroLaboratory of Systems Pharmacology and Department of Systems Biology, Harvard Medical School, Boston, MA 02215, USA.
Peter K SorgerLaboratory of Systems Pharmacology and Department of Systems Biology, Harvard Medical School, Boston, MA 02215, USA.
Erin H SeeleyDepartment of Chemistry, University of Texas at Austin, Austin, TX, USA.
Nicholas NavinDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Robert J DowneyThoracic Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Franziska MichorDepartment of Data Science, Dana-Farber Cancer Institute, Boston, MA 02215, USA.
Harvard University · USThe University of Texas MD Anderson Cancer Center · USBroad Institute · USDana-Farber Cancer Institute · USMemorial Sloan Kettering Cancer Center · USNYU Langone Health · USPeking University · CNThe University of Texas at Austin · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Pharmaco Response Signatures and Disease MechanismU54HL127365 · NHLBI · HARVARD MEDICAL SCHOOL · PI SORGER, PETER KARL · 2014 to 2019
$13.1M
Project 3: Single Cell Measures of Intratumor Diversity for Optimal Breast Cancer TherapyU54CA193461 · NCI · DANA-FARBER CANCER INST · PI POLYAK, KORNELIA · 2015 to 2020
$11.2M
Systems Pharmacology of Therapeutic and Adverse Responses to ImmuneCheckpoint and Small Molecule DrugsU54CA225088 · NCI · HARVARD MEDICAL SCHOOL · PI SORGER, PETER KARL · 2018 to 2022
$10.8M
High dimensional digital pathology to investigate the tumor micro environment and its impact on response to therapyR50CA252138 · NCI · HARVARD MEDICAL SCHOOL · PI MALIGA, ZOLTAN · 2020 to 2024
$1.0M
NCI NIH HHS P30 CA008748NCI NIH HHS R50 CA252138NCI NIH HHS U54 CA193461NCI NIH HHS U54 CA225088NHLBI NIH HHS U54 HL127365
6 · The paper itself

Abstract

Intra-tumor heterogeneity (ITH) of human tumors is important for tumor progression, treatment response, and drug resistance. However, the spatial distribution of ITH remains incompletely understood. Here, we present spatial analysis of ITH in lung adenocarcinomas from 147 patients using multi-region mass spectrometry of >5,000 regions, single-cell copy number sequencing of ~2,000 single cells, and cyclic immunofluorescence of >10 million cells. We identified two distinct spatial patterns among tumors, termed clustered and random geographic diversification (GD). These patterns were observed in the same samples using both proteomic and genomic data. The random proteomic GD pattern, which is characterized by decreased cell adhesion and lower levels of tumor-interacting endothelial cells, was significantly associated with increased risk of recurrence or death in two independent patient cohorts. Our study presents comprehensive spatial mapping of ITH in lung adenocarcinoma and provides insights into the mechanisms and clinical consequences of GD.

Identifiers

PMID36419822
PMCPMC9681138
OpenAlexW4292856186

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.