Evidence map›Paper›PMID 40267200›Full record

ArticleScience advances2025

In vivo functional screens reveal

Lauren Brumage, Scott Best, Daniel S Hippe, Eli Grunblatt, Pritha Chanana, Feinan Wu, Myung Chang Lee, Zhe Ying, Ali Ibrahim, Jae Heun Chung and 7 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The Five-Decade Journey of Small Cell Lung Cancer.Cancer communications (London, England) · 2026
    Review
  7. Review
  8. 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

17 authors.

Lauren BrumageDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0001-9006-4750
Scott BestDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-0461-7919
Daniel S HippeClinical Research Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-2427-4404
Eli GrunblattDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Pritha ChananaGenomics and Bioinformatics Shared Resource, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-2255-8905
Feinan WuGenomics and Bioinformatics Shared Resource, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Myung Chang LeeGenentech, South San Francisco, CA, USA.ORCID 0000-0002-7051-5822
Zhe YingDepartment of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID 0000-0002-0080-5402
Ali IbrahimDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Jae Heun ChungDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-4519-4219
Anna VigilDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-8521-9583
Jackson FatherreeDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Slobodan BeronjaDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Patrick PaddisonDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Lucas SullivanDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-6745-8222
Barzin NabetGenentech, South San Francisco, CA, USA.ORCID 0000-0002-4824-3533
David MacPhersonDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-3729-907X

Funding

Project 4: Risk stratification for pulmonary nodules detected by CT imaging using plasma and imaging biomarkersP50CA228944 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PHILIP D GREENBERG · 2019 to 2026
$19.6M
Identifying and understanding drivers of chemoresistance in small cell lung cancerR01CA281133 · NCI · FRED HUTCHINSON CANCER CENTER · PI David MacPherson · 2023 to 2026
$2.1M
NCI NIH HHS P50 CA228944NCI NIH HHS R01 CA281133
6 · The paper itself

Abstract

Exquisitely chemosensitive initially, small cell lung cancer (SCLC) exhibits dismal outcomes owing to rapid transition to chemoresistance. Elucidating the genetic underpinnings has been challenging owing to limitations with cellular models. As SCLC patient-derived xenograft (PDX) models mimic therapeutic responses, we perform genetic screens in chemosensitive PDX models to identify drivers of chemoresistance. cDNA overexpression screens identify

Indexed as

Drug Resistance, NeoplasmKelch-Like ECH-Associated Protein 1Lung NeoplasmsSmall Cell Lung CarcinomaAnimalsCRISPR-Cas SystemsDNA, ComplementaryFemaleHEK293 CellsHumansImmunologic Deficiency SyndromesMaleMiceProto-Oncogene Proteins c-mycSignal TransductionDNA, ComplementaryKEAP1 protein, humanKelch-Like ECH-Associated Protein 1MYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID40267200
PMCPMC12017300

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.