Evidence map›Paper›PMID 21705107›Full record

ReviewLung cancer (Amsterdam, Netherlands)2011

Do all lung adenocarcinomas follow a stepwise progression?

Yasushi Yatabe, Alain C Borczuk, Charles A Powell

Open access · greenAbstract readReview
In one paragraph

Review in Lung cancer (Amsterdam, Netherlands), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 2 pooled it
8.5field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 2 syntheses or guidelines pooled it, 132 citations in OpenAlex.

  1. Pooled it
  2. [Advance in Diagnose and Treatment Strategies of Adenocarcinoma in Situ].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2017
    Pooled it
  3. Article
  4. Article
  5. Article
  6. Biomolecules & biomedicine · 2025
    Article
  7. Article
  8. eLife · 2025
    Article
  9. Article
  10. Article
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  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Observational
  18. Pan-Driver-Negatives versus Epidermal Growth Factor Receptor Mutants for C-Stage IA Lung Adenocarcinoma with Ground-Glass Opacity.Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia · 2022
    Article
  19. Updates in grading and invasion assessment in lung adenocarcinoma.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2022
    Review
  20. 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

3 authors at 2 institutions in 2 countries.

Yasushi YatabeDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center, 1-1 Kanokoden, Chikusa-ku, Nagoya 464-8681, Japan. yyatabe@aichi-cc.jp
Alain C Borczuk
Charles A Powell
Columbia University Irving Medical Center · USAichi Cancer Center · JP

Funding

Lung Epithelial-Mesenchymal Interactions in Adenocarcinoma InvasionR01CA120174 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI POWELL, CHARLES A. · 2007 to 2011
$1.9M
NCI NIH HHS R01 CA120174
6 · The paper itself

Abstract

Similar to the adenoma-carcinoma sequence of colorectal cancer, lung adenocarcinoma is thought to follow a linear multistep progression, in which a precursor lesion progresses to adenocarcinoma in situ, which is followed by invasive adenocarcinoma. However, lung adenocarcinoma can no longer be considered as a single type of tumor but rather a group of distinct subsets of tumors that arise from different molecular pathways. Consistent with this concept, recent findings revealed that this linear progression might not occur in all lung adenocarcinomas. First, according to the molecular classification based on expression profiling, lung cancer can be divided into at least two subsets; precancerous and in situ lesions share characteristics of molecular expression and clinical features with only one of the two subsets, suggesting that the linear progression is only applicable to the subset in the molecular classification. Second, when EGFR and KRAS were examined based on the progression steps, the mutation rate of KRAS was disproportionally distributed; however, according to the progression schema, gene alterations should be evenly accumulated along the entire progression. Third, by means of comparative genomic hybridization analysis, some adenocarcinoma in situ revealed gene alterations discontinuous to invasive adenocarcinoma. Finally, there were some clinical observations that support that some lesions escape from the progression. In this review, we hypothesize a novel scenario for the progression of lung adenocarcinoma, which does not support a linear progression schema.

Indexed as

Cell Transformation, NeoplasticModels, BiologicalAdenocarcinomaAnimalsCellular SenescenceDisease ProgressionErbB ReceptorsGene Expression ProfilingHumansLung NeoplasmsMutation RateNeoplasm InvasivenessNeoplastic Stem CellsPrecancerous ConditionsProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)EGFR protein, humanErbB ReceptorsKRAS protein, humanProto-Oncogene ProteinsProto-Oncogene Proteins p21(ras)ras Proteins

Identifiers

PMID21705107
PMCPMC3172366
OpenAlexW2161042246

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.