Evidence map›Paper›PMID 25823023›Full record

ReviewOncogene2015

Lineage factors and differentiation states in lung cancer progression.

W K C Cheung, D X Nguyen

Abstract readReview
In one paragraph

Review in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

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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

2 authors.

W K C CheungDepartment of Pathology, Pathology and Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
D X NguyenDepartment of Pathology, Pathology and Cancer Center, Yale University School of Medicine, New Haven, CT, USA.

Funding

A Novel Lineage Specific Metastasis Suppressor Pathway in Lung CancerR01CA166376 · NCI · YALE UNIVERSITY · PI NGUYEN, DON X · 2012 to 2024
$3.8M
A novel lineage pathway controls metabolic adaptation by metastatic lung cancersR01CA191489 · NCI · YALE UNIVERSITY · PI NGUYEN, DON X · 2015 to 2019
$1.9M
NCI NIH HHS 1R01CA166376NCI NIH HHS 1R01CA191489NCI NIH HHS 1R21CA170537NCI NIH HHS R01 CA166376NCI NIH HHS R01 CA191489
6 · The paper itself

Abstract

Lung cancer encompasses a heterogeneous group of malignancies. Here we discuss how the remarkable diversity of major lung cancer subtypes is manifested in their transforming cell of origin, oncogenic dependencies, phenotypic plasticity, metastatic competence and response to therapy. More specifically, we review the increasing evidence that links this biological heterogeneity to the deregulation of cell lineage-specific pathways and the transcription factors that ultimately control them. As determinants of pulmonary epithelial differentiation, these poorly characterized transcriptional networks may underlie the etiology and biological progression of distinct lung cancers, while providing insight into innovative therapeutic strategies.

Indexed as

Cell DifferentiationCell LineageDisease ProgressionHepatocytesHumansLung NeoplasmsSignal TransductionTranscription FactorsTranscription Factors

Identifiers

PMID25823023
PMCPMC7597437

What OpenQuestion holds

Textmetadata
LicenceTDM
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.