Evidence map›Paper›PMID 32191822›Full record

ArticleMolecular oncology2021

Genomic and pathological heterogeneity in clinically diagnosed small cell lung cancer in never/light smokers identifies therapeutically targetable alterations.

Atsuko Ogino, Jihyun Choi, Mika Lin, Margaret K Wilkens, Antonio Calles, Man Xu, Anika E Adeni, Emily S Chambers, Marzia Capelletti, Mohit Butaney and 7 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Myricetin activates the Caspase-3/GSDME pathwayFrontiers in pharmacology · 2022
    Article
  10. ERK Inhibitor LY3214996-Based Treatment Strategies forMolecular cancer therapeutics · 2021
    Article
  11. Article
  12. 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 at 3 institutions in 1 country.

Atsuko OginoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Jihyun ChoiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Mika LinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Margaret K WilkensExperimental Therapeutics Core, Dana-Farber Cancer Institute, Boston, MA, USA.
Antonio CallesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-2547-1947
Man XuBelfer Center for Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Anika E AdeniDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Emily S ChambersDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Marzia CapellettiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Mohit ButaneyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Nathanael S GrayDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA, USA.
Prafulla C GokhaleExperimental Therapeutics Core, Dana-Farber Cancer Institute, Boston, MA, USA.
Sangeetha PalakurthiBelfer Center for Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Paul KirschmeierBelfer Center for Applied Cancer Science, Dana-Farber Cancer Institute, Boston, MA, USA.
Geoffrey R OxnardDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Lynette M ShollDepartment of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
Pasi A JänneDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-7821-4928
Dana-Farber Cancer Institute · USBrigham and Women's Hospital · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small-cell lung cancer (SCLC) occurs infrequently in never/former light smokers. We sought to study this rare clinical subset through next-generation sequencing (NGS) and by characterizing a representative patient-derived model. We performed targeted NGS, as well as comprehensive pathological evaluation, in 11 never/former light smokers with clinically diagnosed SCLC. We established a patient-derived model from one such patient (DFCI168) harboring an NRAS

Indexed as

Genetic HeterogeneityMolecular Targeted TherapySmokersAgedAnimalsBase SequenceCell Line, TumorCell SurvivalDrug SynergismFemaleGTP PhosphohydrolasesHumansLung NeoplasmsMaleMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2GTP PhosphohydrolasesMechanistic Target of Rapamycin Complex 1Mechanistic Target of Rapamycin Complex 2Membrane ProteinsMitogen-Activated Protein Kinase KinasesNRAS protein, humanProtein Kinase Inhibitorscombination therapylung cancers in never smokersnon-neuroendocrine SCLCRAS mutationsmall-cell lung cancer

Identifiers

PMID32191822
PMCPMC7782083
OpenAlexW3012369876

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.