Evidence map›Paper›PMID 36778670›Full record

ArticleCell genomics2022

Multi-hallmark long noncoding RNA maps reveal non-small cell lung cancer vulnerabilities.

Roberta Esposito, Taisia Polidori, Dominik F Meise, Carlos Pulido-Quetglas, Panagiotis Chouvardas, Stefan Forster, Paulina Schaerer, Andrea Kobel, Juliette Schlatter, Erik Kerkhof and 19 more

Abstract 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 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  7. Review
  8. Nucleic acid drugs: recent progress and future perspectives.Signal transduction and targeted therapy · 2024
    Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. TheNon-coding RNA · 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

29 authors.

Roberta EspositoDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Taisia PolidoriDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Dominik F MeiseDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Carlos Pulido-QuetglasDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Panagiotis ChouvardasDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Stefan ForsterDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Paulina SchaererDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Andrea KobelDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Juliette SchlatterDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Erik KerkhofDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Michaela RoemmeleDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Emily S RiceDepartment of Microbiology, Immunology, and Cell Biology, Morgantown, WV, USA.
Lina ZhuDepartment of Surgery, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong.
Andrés LanzósDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Hugo A Guillen-RamirezDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Giulia BasileDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Irene CarrozzoDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Adrienne VancuraDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Sebastian UllrichCentre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology (BIST), Barcelona, Catalonia 08003, Spain.
Alvaro AndradesGENYO, Centre for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government, Granada 18016, Spain.
Dylan HarveySchool of Biology and Environmental Science, University College Dublin, Dublin D04 V1W8, Ireland.
Pedro P MedinaGENYO, Centre for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government, Granada 18016, Spain.
Patrick C MaPenn State Cancer Institute, Hershey, PA 17033, USA.
Simon HaefligerDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Xin WangDepartment of Surgery, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong.
Ivan MartinezDepartment of Microbiology, Immunology, and Cell Biology, Morgantown, WV, USA.
Adrian F OchsenbeinDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Carsten RietherDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.
Rory JohnsonDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern 3010 Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long noncoding RNAs (lncRNAs) are widely dysregulated in cancer, yet their functional roles in cancer hallmarks remain unclear. We employ pooled CRISPR deletion to perturb 831 lncRNAs detected in KRAS-mutant non-small cell lung cancer (NSCLC) and measure their contribution to proliferation, chemoresistance, and migration across two cell backgrounds. Integrative analysis of these data outperforms conventional "dropout" screens in identifying cancer genes while prioritizing disease-relevant lncRNAs with pleiotropic and background-independent roles. Altogether, 80 high-confidence oncogenic lncRNAs are active in NSCLC, which tend to be amplified and overexpressed in tumors. A follow-up antisense oligonucleotide (ASO) screen shortlisted two candidates,

Indexed as

antisense oligonucleotidescancerCRISPRlncRNAlong noncoding RNAnon-small cell lung cancerNSCLCRNA therapeutics

Identifiers

PMID36778670
PMCPMC9903773

What OpenQuestion holds

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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.