Evidence map›Paper›PMID 35383171›Full record

ArticleNature communications2022

Integrative analysis of non-small cell lung cancer patient-derived xenografts identifies distinct proteotypes associated with patient outcomes.

Shideh Mirhadi, Shirley Tam, Quan Li, Nadeem Moghal, Nhu-An Pham, Jiefei Tong, Brian J Golbourn, Jonathan R Krieger, Paul Taylor, Ming Li and 17 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

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

  1. Pooled it
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  8. Microfabricated Organ-Specific Models of Tumor Microenvironments.Annual review of biomedical engineering · 2025
    Review
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  20. iScience · 2023
    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

27 authors at 5 institutions in 2 countries.

Shideh MirhadiProgram in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Shirley TamPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Quan LiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Nadeem MoghalPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Nhu-An PhamPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Jiefei TongProgram in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Brian J GolbournJohn G. Rangos Sr. Research Center, Children's Hospital of Pittsburgh, and Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Jonathan R KriegerSPARC BioCentre, Hospital for Sick Children, Toronto, ON, Canada.
Paul TaylorProgram in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.
Ming LiPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Jessica WeissDepartment of Biostatistics, Princess Margaret Cancer Centre, Toronto, ON, Canada.
Sebastiao N Martins-FilhoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-6123-2601
Vibha RaghavanPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Yasin MamatjanPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-8807-2927
Aafaque A KhanProgram in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-8127-9677
Michael CabaneroPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Shingo SakashitaPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Kugeng HuoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Sameer AgnihotriJohn G. Rangos Sr. Research Center, Children's Hospital of Pittsburgh, and Department of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.ORCID http://orcid.org/0000-0001-6584-3795
Kota IshizawaDivision of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Thomas K WaddellDivision of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-3235-9208
Gelareh ZadehPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-6637-4502
Kazuhiro YasufukuDivision of Thoracic Surgery, Toronto General Hospital, University Health Network, Toronto, ON, Canada.
Geoffrey LiuPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Frances A ShepherdPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Michael F MoranProgram in Cell Biology, Hospital for Sick Children, Toronto, ON, Canada. m.moran@utoronto.ca.ORCID http://orcid.org/0000-0003-4878-9285
Ming-Sound TsaoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada. ming.tsao@uhn.ca.ORCID http://orcid.org/0000-0002-9160-5405
University Health Network · CAHospital for Sick Children · CAUniversity of Pittsburgh · USUniversity of Toronto · CAPrincess Margaret Cancer Centre · CA

Funding

CIHR FDN-148395
6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is the leading cause of cancer deaths worldwide. Only a fraction of NSCLC harbor actionable driver mutations and there is an urgent need for patient-derived model systems that will enable the development of new targeted therapies. NSCLC and other cancers display profound proteome remodeling compared to normal tissue that is not predicted by DNA or RNA analyses. Here, we generate 137 NSCLC patient-derived xenografts (PDXs) that recapitulate the histology and molecular features of primary NSCLC. Proteome analysis of the PDX models reveals 3 adenocarcinoma and 2 squamous cell carcinoma proteotypes that are associated with different patient outcomes, protein-phosphotyrosine profiles, signatures of activated pathways and candidate targets, and in adenocarcinoma, stromal immune features. These findings portend proteome-based NSCLC classification and treatment and support the PDX resource as a viable model for the development of new targeted therapies.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAnimalsHeterograftsHumansMiceMice, SCIDXenograft Model Antitumor Assays

Identifiers

PMID35383171
PMCPMC8983714
OpenAlexW4224315996

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.