Evidence map›Paper›PMID 16705311›Full record

ArticleBritish journal of cancer2006

Differential disruption of cell cycle pathways in small cell and non-small cell lung cancer.

B P Coe, W W Lockwood, L Girard, R Chari, C Macaulay, S Lam, A F Gazdar, J D Minna, W L Lam

Open access · hybridAbstract readComparative Study
In one paragraph

Article in British journal of cancer, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.5field-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

45 citing papers in PubMed, 82 citations in OpenAlex.

  1. Article
  2. Review
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  6. Article
  7. Article
  8. Article
  9. Article
  10. Integrative Genomic Analyses Identifies GGA2 as a Cooperative Driver of EGFR-Mediated Lung Tumorigenesis.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. E2F8 as a Novel Therapeutic Target for Lung Cancer.Journal of the National Cancer Institute · 2015
    Article
  15. EZH2 promotes E2F-driven SCLC tumorigenesis through modulation of apoptosis and cell-cycle regulation.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2013
    Article
  16. Article
  17. Article
  18. Review
  19. Article
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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

9 authors at 3 institutions in 2 countries.

B P CoeDepartment of Cancer Genetics and Developmental Biology, British Columbia Cancer Research Center, Vancouver, Canada. bcoe@bccrc.ca
W W Lockwood
L Girard
R Chari
C Macaulay
S Lam
A F Gazdar
J D Minna
W L Lam
University of British Columbia · CAThe University of Texas Southwestern Medical Center · USBC Cancer Agency · CA

Funding

UNIVERSITY OF TEXAS--SPORE IN LUNG CANCERP50CA070907 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI GIBBONS, DON LYNN · 1996 to 2024
$57.4M
A Phase II Trial of ACAPHA in Former Smokers with IEN.U01CA096109 · NCI · BRITISH COLUMBIA CANCER AGENCY · PI LAM, STEPHEN C · 2002 to 2006
$4.6M
NCI NIH HHS 1U01CA96109NCI NIH HHS P50 CA070907NCI NIH HHS P50CA70907NCI NIH HHS U01 CA096109
6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related mortality in the world, with small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC) comprising the two major cell types. Although these cell types can be distinguished readily at the histological level, knowledge of their underlying molecular differences is very limited. In this study, we compared 14 SCLC cell lines against 27 NSCLC cell lines using an integrated array comparative genomic hybridisation and gene expression profiling approach to identify subtype-specific disruptions. Using stringent criteria, we have identified 159 of the genes that are responsible for the different biology of these cell types. Sorting of these genes by their biological functions revealed the differential disruption of key components involved in cell cycle pathways. Our novel comparative combined genome and transcriptome analysis not only identified differentially altered genes, but also revealed that certain shared pathways are preferentially disrupted at different steps in these cell types. Small cell lung cancer exhibited increased expression of MRP5, activation of Wnt pathway inhibitors, and upregulation of p38 MAPK activating genes, while NSCLC showed downregulation of CDKN2A, and upregulation of MAPK9 and EGFR. This information suggests that cell cycle upregulation in SCLC and NSCLC occurs through drastically different mechanisms, highlighting the need for differential molecular target selection in the treatment of these cancers.

Indexed as

Genes, NeoplasmCarcinoma, Non-Small-Cell LungCarcinoma, Small CellCell CycleCell Line, TumorGene DosageGene ExpressionGene Expression ProfilingHumansLung NeoplasmsNucleic Acid HybridizationPrincipal Component AnalysisReverse Transcriptase Polymerase Chain Reaction

Identifiers

PMID16705311
PMCPMC2361340
OpenAlexW2055645461

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.