Evidence map›Paper›PMID 31827074›Full record

ReviewExperimental & molecular medicine2019

Recent progress in mapping the emerging landscape of the small-cell lung cancer genome.

Kee-Beom Kim, Colin T Dunn, Kwon-Sik Park

Open access · goldAbstract readReview
In one paragraph

Review in Experimental & molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

70 citing papers in PubMed, 122 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Synthetic lethality between RB-loss and E2F3 inhibition in small cell cancers targeted by pyrimidine synthesis blockade.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

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

3 authors at 2 institutions in 1 country.

Kee-Beom KimDepartments of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA.
Colin T DunnSchool of Medicine MD Program, Case Western Reserve University, Cleveland, OH, 44106, USA.
Kwon-Sik ParkDepartments of Microbiology, Immunology, and Cancer Biology, University of Virginia School of Medicine, Charlottesville, VA, 22908, USA. kp5an@virginia.edu.ORCID http://orcid.org/0000-0003-3346-9086
University of Virginia · USCase Western Reserve University · US

Funding

Targeting BCAT1 and branched-chain amino acid metabolism for the detection and prevention of SCLCU01CA224293 · NCI · UNIVERSITY OF VIRGINIA · PI PARK, KWON-SIK · 2018 to 2022
$2.2M
(PQ4A) Metabolic Plasticity of Pre-Malignant Cells During Tumor ProgressionR01CA194461 · NCI · UNIVERSITY OF VIRGINIA · PI PARK, KWON-SIK · 2015 to 2018
$1.6M
Engineered precancerous cells and tissues for discovery of lung cancer driversR03CA215777 · NCI · UNIVERSITY OF VIRGINIA · PI PARK, KWON-SIK · 2017 to 2018
$161k
American Cancer Society (American Cancer Society, Inc.) RSG-15-066-01-TBGNCI NIH HHS R01 CA194461NCI NIH HHS R03 CA215777NCI NIH HHS U01 CA224293
6 · The paper itself

Abstract

Small-cell lung cancer (SCLC) remains the deadliest of all the lung cancer types. Its high mortality is largely attributed to the invariable development of resistance to standard chemo/radiotherapies, which have remained unchanged for the past 30 years, underscoring the need for new therapeutic approaches. The discovery of molecular targets for chemoprevention and treatment has been hampered by the poor understanding of SCLC progression. In recent years, comprehensive omics-based analyses have led to the discovery of recurrent alterations in patient tumors, and functional studies using genetically engineered mouse models and patient-derived tumor models have provided information about the alterations critical for SCLC pathogenesis. Defining the somatic alterations scattered throughout the SCLC genome will help to understand the underlying mechanism of this devastating disease and pave the way for the discovery of therapeutic vulnerabilities associated with the genomic alterations.

Indexed as

AnimalsEpigenomicsHumansLung NeoplasmsMutationSmall Cell Lung Carcinoma

Identifiers

PMID31827074
PMCPMC6906379
OpenAlexW2994783399

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.