Evidence map›Paper›PMID 23674306›Full record

ArticleGenome research2013

Proteome-wide discovery of mislocated proteins in cancer.

KiYoung Lee, Kyunghee Byun, Wonpyo Hong, Han-Yu Chuang, Chan-Gi Pack, Enkhjargal Bayarsaikhan, Sun Ha Paek, Hyosil Kim, Hye Young Shin, Trey Ideker and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 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.

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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. dbMisLoc: A Manually Curated Database of Conditional Protein Mis-localization Events.Interdisciplinary sciences, computational life sciences · 2023
    Article
  7. Article
  8. Article
  9. KIF13A-A Key Regulator of Recycling Endosome Dynamics.Frontiers in cell and developmental biology · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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  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

11 authors at 5 institutions in 3 countries.

KiYoung LeeDepartment of Biomedical Informatics, Ajou University School of Medicine, Suwon 443-749, Korea. kiylee@ajou.ac.kr
Kyunghee Byun
Wonpyo Hong
Han-Yu Chuang
Chan-Gi Pack
Enkhjargal Bayarsaikhan
Sun Ha Paek
Hyosil Kim
Hye Young Shin
Trey Ideker
Bonghee Lee
Ajou University · KRGachon University · KRSeoul National University Hospital · KRUniversity of California San Diego · USRIKEN Advanced Science Institute · JP

Funding

Cytoscape: A Modeling Platform for Biomolecular NetworksR01GM070743 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI IDEKER, TREY · 2004 to 2016
$5.7M
NIGMS NIH HHS GM070743NIGMS NIH HHS R01 GM070743
6 · The paper itself

Abstract

Several studies have sought systematically to identify protein subcellular locations, but an even larger task is to map which of these proteins conditionally relocates in disease (the mislocalizome). Here, we report an integrative computational framework for mapping conditional location and mislocation of proteins on a proteome-wide scale, called a conditional location predictor (CoLP). Using CoLP, we mapped the locations of over 10,000 proteins in normal human brain and in glioma. The prediction showed 0.9 accuracy using 100 location tests of 20 randomly selected proteins. Of the 10,000 proteins, over 150 have a strong likelihood of mislocation under glioma, which is striking considering that few mislocation events have been identified in this disease previously. Using immunofluorescence and Western blotting in both primary cells and tissues, we successfully experimentally confirmed 15 mislocations. The most common type of mislocation occurs between the endoplasmic reticulum and the nucleus; for example, for RNF138, TLX3, and NFRKB. In particular, we found that the gene for the mislocating protein GFRA4 had a nonsynonymous point mutation in exon 2. Moreover, redirection of GFRA4 to its normal location, the plasma membrane, led to marked reductions in phospho-STAT3 and proliferation of glioma cells. This framework has the potential to track changes in protein location in many human diseases.

Indexed as

BrainBrain NeoplasmsCell ProliferationDisease ProgressionGene OntologyGlial Cell Line-Derived Neurotrophic Factor ReceptorsGliomaHomeobox Protein Nkx-2.2Homeodomain ProteinsHumansKinesinsMolecular Sequence AnnotationNerve Tissue ProteinsProtein TransportProteomeProto-Oncogene Proteins c-retGFRA4 protein, humanGlial Cell Line-Derived Neurotrophic Factor ReceptorsHomeobox Protein Nkx-2.2Homeodomain ProteinsKIF13A protein, humanKinesinsNerve Tissue ProteinspersephinProteomeProto-Oncogene Proteins c-retRET protein, humanRNF138 protein, humanSTAT3 protein, humanSTAT3 Transcription FactorTranscription FactorsUbiquitin-Protein LigasesZebrafish Proteins

Identifiers

PMID23674306
PMCPMC3730102
OpenAlexW2154459622

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.