Evidence map›Paper›PMID 32579974›Full record

ArticleCell2020

Multimodal Analysis of Composition and Spatial Architecture in Human Squamous Cell Carcinoma.

Andrew L Ji, Adam J Rubin, Kim Thrane, Sizun Jiang, David L Reynolds, Robin M Meyers, Margaret G Guo, Benson M George, Annelie Mollbrink, Joseph Bergenstråhle and 11 more

Erratum issued Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05986461 (Spatially Resolved Transcriptomics Reveals Phenotype-specific Molecular Signatures in Complex Regional Pain Syndrome), which is not on this map. Cited by 634 papers.

0numbers the graph read from it
0cells of the map it votes in
634citing papers in PubMed
46.1field-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.

NCT05986461 unknown statusnot on this mapstarted 2023, after this paper: background citation

Spatially Resolved Transcriptomics Reveals Phenotype-specific Molecular Signatures in Complex Regional Pain Syndrome

Typeobservational_patient_registrySponsorSeoul National UniversityRan2023 to 2024Enrolled10ConditionsComplex Regional Pain Syndromes
3 · Its place in the literature

Who cites it

634 citing papers in PubMed, 1,073 citations in OpenAlex.

  1. Article
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  4. Review
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  6. Review
  7. Insights Into Spatial Transcriptomics: Exploring Recent Technical Developments and Their Diverse Applications.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  8. Article
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  11. Review
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  19. Article
  20. Unified representation learning for spatial multi-omics.Bioinformatics (Oxford, England) · 2026
    Article

574 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 4 institutions in 2 countries.

Andrew L JiProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Adam J RubinProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Kim ThraneScience for Life Laboratory, KTH Royal Institute of Technology, Department of Gene Technology, Tomtebodavägen 23, 171 65 Solna, Sweden.
Sizun JiangDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
David L ReynoldsProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Robin M MeyersProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Margaret G GuoProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Benson M GeorgeInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.
Annelie MollbrinkScience for Life Laboratory, KTH Royal Institute of Technology, Department of Gene Technology, Tomtebodavägen 23, 171 65 Solna, Sweden.
Joseph BergenstråhleScience for Life Laboratory, KTH Royal Institute of Technology, Department of Gene Technology, Tomtebodavägen 23, 171 65 Solna, Sweden.
Ludvig LarssonScience for Life Laboratory, KTH Royal Institute of Technology, Department of Gene Technology, Tomtebodavägen 23, 171 65 Solna, Sweden.
Yunhao BaiDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Bokai ZhuDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Aparna BhaduriDepartment of Neurology, University of California, San Francisco (UCSF), San Francisco, CA 94122, USA.
Jordan M MeyersProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Xavier Rovira-ClavéDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
S Tyler HollmigProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Sumaira Z AasiProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Garry P NolanDepartment of Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Joakim LundebergScience for Life Laboratory, KTH Royal Institute of Technology, Department of Gene Technology, Tomtebodavägen 23, 171 65 Solna, Sweden.
Paul A KhavariProgram in Epithelial Biology, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Veterans Affairs Palo Alto Healthcare System, Palo Alto, CA, USA. Electronic address: khavari@stanford.edu.
Stanford University · USScience for Life Laboratory · SEKTH Royal Institute of Technology · SEUniversity of California, San Francisco · US

Funding

Using a tonsil organoid system to probe conditions for the induction of protective antibody and T cell responses to influenza.U19AI057229 · NIAID · STANFORD UNIVERSITY · PI Mark Morris Davis · 2003 to 2026
$88.5M
Systems Biology CoreU19AI100627 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI ULEVITCH, RICHARD J · 2012 to 2021
$49.1M
Technology CoreU19AI135976 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI ADEREM, ALAN A · 2018 to 2022
$17.0M
The Cellular Geography of Therapeutic Resistance in CancerU2CCA233195 · NCI · DANA-FARBER CANCER INST · PI JOHNSON, BRUCE E. · 2018 to 2023
$13.7M
Mechanisms of Epidermal Homeostasis and Early NeoplasiaR01AR043799 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1998 to 2026
$9.1M
Project 3: Identifying plasma biomarkers predicting time to HIV rebound after treatment interruptionP01AI131374 · NIAID · J. DAVID GLADSTONE INSTITUTES · PI PILLAI, SATISH KUMAR · 2017 to 2021
$8.5M
The Lung PCA: A Multi-Dimensional Atlas of Pulmonary PremalignancyU2CCA233238 · NCI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI DUBINETT, STEVEN M., SPIRA, AVRUM E · 2018 to 2021
$7.0M
Stanford Tissue Mapping CenterU54HG010426 · NHGRI · STANFORD UNIVERSITY · PI SNYDER, MICHAEL P. · 2018 to 2021
$5.1M
Tissue Cytokine Sequestration and Immune Regulation in AutoimmunityU01AI101984 · NIAID · STANFORD UNIVERSITY · PI BOLLYKY, PAUL L · 2012 to 2021
$5.0M
Postgraduate Training Program in Epithelial BiologyT32AR007422 · NIAMS · STANFORD UNIVERSITY · PI PAUL KHAVARI · 1986 to 2026
$5.0M
Multiscale Modeling of Myelodysplastic SyndromesR01HL128173 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COREY, SETH JOEL, KIMMEL, MAREK · 2015 to 2019
$3.8M
Balanced signaling cues to guide cell transitions in the blood lineage continuumR01HL120724 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHAKRABORTY, ARUP K., NOLAN, GARRY P · 2015 to 2019
$3.7M
Cancer Research UK 27145Cancer Research UK C27165/A29073NCI NIH HHS F32 CA233203NCI NIH HHS F99 CA212231NCI NIH HHS R01 CA142635NCI NIH HHS R33 CA183692NCI NIH HHS U2C CA233195NCI NIH HHS U2C CA233238NHGRI NIH HHS U54 HG010426NHLBI NIH HHS R01 HL120724NHLBI NIH HHS R01 HL128173NIAID NIH HHS P01 AI131374NIAID NIH HHS U01 AI101984NIAID NIH HHS U01 AI140498NIAID NIH HHS U19 AI057229NIAID NIH HHS U19 AI100627NIAID NIH HHS U19 AI135976NIAMS NIH HHS R01 AR043799NIAMS NIH HHS T32 AR007422NIDDK NIH HHS UG3 DK114937NIH HHS S10 OD018220
6 · The paper itself

Abstract

To define the cellular composition and architecture of cutaneous squamous cell carcinoma (cSCC), we combined single-cell RNA sequencing with spatial transcriptomics and multiplexed ion beam imaging from a series of human cSCCs and matched normal skin. cSCC exhibited four tumor subpopulations, three recapitulating normal epidermal states, and a tumor-specific keratinocyte (TSK) population unique to cancer, which localized to a fibrovascular niche. Integration of single-cell and spatial data mapped ligand-receptor networks to specific cell types, revealing TSK cells as a hub for intercellular communication. Multiple features of potential immunosuppression were observed, including T regulatory cell (Treg) co-localization with CD8 T cells in compartmentalized tumor stroma. Finally, single-cell characterization of human tumor xenografts and in vivo CRISPR screens identified essential roles for specific tumor subpopulation-enriched gene networks in tumorigenesis. These data define cSCC tumor and stromal cell subpopulations, the spatial niches where they interact, and the communicating gene networks that they engage in cancer.

Indexed as

AnimalsCarcinoma, Squamous CellCell Line, TumorClustered Regularly Interspaced Short Palindromic RepeatsGenomicsHumansKeratinocytesMiceRNA-SeqSingle-Cell AnalysisSkinSkin NeoplasmsTranscriptomeTransplantation, HeterologousCRISPR screenintra-tumoral heterogeneityMIBImulti-omicsscRNA-seqskin cancerspatial transcriptomicssquamous cell carcinomatumor immunologytumor microenvironment

Identifiers

PMID32579974
PMCPMC7391009
OpenAlexW3036371598

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.