Evidence map›Paper›PMID 34650042›Full record

ArticleNature communications2021

Spatial deconvolution of HER2-positive breast cancer delineates tumor-associated cell type interactions.

Alma Andersson, Ludvig Larsson, Linnea Stenbeck, Fredrik Salmén, Anna Ehinger, Sunny Z Wu, Ghamdan Al-Eryani, Daniel Roden, Alex Swarbrick, Åke Borg and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 256 papers.

0numbers the graph read from it
0cells of the map it votes in
256citing papers in PubMed
20.8field-weighted citation impact, top 1% 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

256 citing papers in PubMed, 380 citations in OpenAlex.

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  14. Investigating Spatial Dynamics in Spatial Omics Data with StarTrail.Journal of the American Statistical Association · 2026
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196 more citing papers are in PubMed but not listed here.

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

13 authors at 5 institutions in 3 countries.

Alma Andersson *Science for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden.
Ludvig Larsson *Science for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0003-4209-2911
Linnea Stenbeck *Science for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden.ORCID 0000-0002-0210-7886
Fredrik SalménScience for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden.
Anna EhingerDepartment of Genetics and Pathology, Laboratory Medicine Region Skåne, Lund, Sweden.ORCID 0000-0001-9225-7396
Sunny Z WuThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, Australia.ORCID 0000-0002-6153-0449
Ghamdan Al-EryaniThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, Australia.ORCID 0000-0002-1137-1726
Daniel RodenThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, Australia.ORCID 0000-0003-2393-5805
Alex SwarbrickThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, Australia.ORCID 0000-0002-3051-5676
Åke BorgDepartment of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.
Jonas FrisénDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Camilla EngblomDepartment of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-5090-4161
Joakim LundebergScience for Life Laboratory, Division of Gene Technology, KTH Royal Institute of Technology, Stockholm, Sweden. joakim.lundeberg@scilifelab.se.ORCID 0000-0003-4313-1601
Garvan Institute of Medical Research · AUScience for Life Laboratory · SEKarolinska Institutet · SELund University · SERoyal Netherlands Academy of Arts and Sciences · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the past decades, transcriptomic studies have revolutionized cancer treatment and diagnosis. However, tumor sequencing strategies typically result in loss of spatial information, critical to understand cell interactions and their functional relevance. To address this, we investigate spatial gene expression in HER2-positive breast tumors using Spatial Transcriptomics technology. We show that expression-based clustering enables data-driven tumor annotation and assessment of intra- and interpatient heterogeneity; from which we discover shared gene signatures for immune and tumor processes. By integration with single cell data, we spatially map tumor-associated cell types to find tertiary lymphoid-like structures, and a type I interferon response overlapping with regions of T-cell and macrophage subset colocalization. We construct a predictive model to infer presence of tertiary lymphoid-like structures, applicable across tissue types and technical platforms. Taken together, we combine different data modalities to define a high resolution map of cellular interactions in tumors and provide tools generalizing across tissues and diseases.

Indexed as

TranscriptomeBreast NeoplasmsCluster AnalysisErb-b2 Receptor Tyrosine KinasesFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenetic HeterogeneityHumansERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID34650042
PMCPMC8516894
OpenAlexW3205213119

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.