Evidence map›Paper›PMID 22194472›Full record

ArticleGenome research2012

A transforming KIF5B and RET gene fusion in lung adenocarcinoma revealed from whole-genome and transcriptome sequencing.

Young Seok Ju, Won-Chul Lee, Jong-Yeon Shin, Seungbok Lee, Thomas Bleazard, Jae-Kyung Won, Young Tae Kim, Jong-Il Kim, Jin-Hyoung Kang, Jeong-Sun Seo

Registry-linked trialOpen access · hybridAbstract readCase Reports
In one paragraph

Article in Genome research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01823068 (A Phase II Study of Vandetanib in Patients With Non-small Cell Lung Cancer Harboring RET Rearrangement), which is not on this map. Cited by 234 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
234citing papers in PubMed, 3 pooled it
–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.

NCT01823068 phase2completednot on this mapstarted 2014, after this paper: background citation

A Phase II Study of Vandetanib in Patients With Non-small Cell Lung Cancer Harboring RET Rearrangement

TypeinterventionalSponsorSamsung Medical CenterRan2014 to 2018Enrolled17ConditionsNon Small Cell Lung CancerArmsVandetanib
3 · Its place in the literature

Who cites it

234 citing papers in PubMed, 3 syntheses or guidelines pooled it, 483 citations in OpenAlex.

  1. Pooled it
  2. Mutation incidence and coincidence in non small-cell lung cancer: meta-analyses by ethnicity and histology (mutMap).Annals of oncology : official journal of the European Society for Medical Oncology · 2013
    Pooled it
  3. Guideline
  4. An improved assay for detection of theranostic gene translocations and MET exon 14 skipping in thoracic oncology.Laboratory investigation; a journal of technical methods and pathology · 2021
    Trial
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  7. Molecular profiling and targeted therapy for advanced thoracic malignancies: a biomarker-derived, multiarm, multihistology phase II basket trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2015
    Trial
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  10. Trial
  11. Review
  12. AccurateInternational journal of molecular sciences · 2025
    Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. JTO clinical and research reports · 2024
    Article
  20. Article

174 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

10 authors at 3 institutions in 3 countries.

Young Seok JuGenomic Medicine Institute, Medical Research Center, Seoul National University, Seoul, Korea.
Won-Chul Lee
Jong-Yeon Shin
Seungbok Lee
Thomas Bleazard
Jae-Kyung Won
Young Tae Kim
Jong-Il Kim
Jin-Hyoung Kang
Jeong-Sun Seo
Seoul National University · KRSeoul National University Hospital · KRThe Catholic University of Korea Seoul St. Mary's Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of the molecular events that drive cancer transformation is essential to the development of targeted agents that improve the clinical outcome of lung cancer. Many studies have reported genomic driver mutations in non-small-cell lung cancers (NSCLCs) over the past decade; however, the molecular pathogenesis of >40% of NSCLCs is still unknown. To identify new molecular targets in NSCLCs, we performed the combined analysis of massively parallel whole-genome and transcriptome sequencing for cancer and paired normal tissue of a 33-yr-old lung adenocarcinoma patient, who is a never-smoker and has no familial cancer history. The cancer showed no known driver mutation in EGFR or KRAS and no EML4-ALK fusion. Here we report a novel fusion gene between KIF5B and the RET proto-oncogene caused by a pericentric inversion of 10p11.22-q11.21. This fusion gene overexpresses chimeric RET receptor tyrosine kinase, which could spontaneously induce cellular transformation. We identified the KIF5B-RET fusion in two more cases out of 20 primary lung adenocarcinomas in the replication study. Our data demonstrate that a subset of NSCLCs could be caused by a fusion of KIF5B and RET, and suggest the chimeric oncogene as a promising molecular target for the personalized diagnosis and treatment of lung cancer.

Indexed as

AdenocarcinomaAdultAlternative SplicingBase SequenceChromosome BreakpointsChromosomes, Human, Pair 10ExonsGene OrderGenome, HumanHigh-Throughput Nucleotide SequencingHumansKinesinsLung NeoplasmsMaleModels, MolecularOncogene Proteins, FusionKIF5B protein, humanKIF5B-RET fusion protein, humanKinesinsMAS1 protein, humanOncogene Proteins, FusionProtein-Tyrosine KinasesProto-Oncogene MasProto-Oncogene Proteins c-ret

Identifiers

PMID22194472
PMCPMC3290779
OpenAlexW2122133689

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.