Evidence map›Paper›PMID 27982029›Full record

ArticleNature communications2016

GALNT14 promotes lung-specific breast cancer metastasis by modulating self-renewal and interaction with the lung microenvironment.

Ki-Hoon Song, Mi So Park, Tulip S Nandu, Shrikanth Gadad, Sang-Cheol Kim, Mi-Young Kim

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

69 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
  2. Review
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  5. GalNAc-Transferases in Cancer.Biomedicines · 2025
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  7. Mechanistic study ofTranslational andrology and urology · 2025
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  10. Journal of hepatocellular carcinoma · 2025
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
  20. Cell-cell communication characteristics in breast cancer metastasis.Cell communication and signaling : CCS · 2024
    Review

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Ki-Hoon SongDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejon 305-701, Korea.
Mi So ParkDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejon 305-701, Korea.
Tulip S NanduCecil H. and Ida Green Center for Reproductive Biology Sciences and Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Shrikanth GadadCecil H. and Ida Green Center for Reproductive Biology Sciences and Division of Basic Reproductive Biology Research, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA.
Sang-Cheol KimDepartment of Biomedical Informatics, Center for Genome Science, National Institute of Health, KCDC, Choongchung-Buk-do 363-951, Korea.
Mi-Young KimDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology (KAIST), Daejon 305-701, Korea.
Korea Advanced Institute of Science and Technology · KRThe University of Texas Southwestern Medical Center · USKorea National Institute of Health · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Some polypeptide N-acetyl-galactosaminyltransferases (GALNTs) are associated with cancer, but their function in organ-specific metastasis remains unclear. Here, we report that GALNT14 promotes breast cancer metastasis to the lung by enhancing the initiation of metastatic colonies as well as their subsequent growth into overt metastases. Our results suggest that GALNT14 augments the self-renewal properties of breast cancer cells (BCCs). Furthermore, GALNT14 overcomes the inhibitory effect of lung-derived bone morphogenetic proteins (BMPs) on self-renewal and therefore facilitates metastasis initiation within the lung microenvironment. In addition, GALNT14 supports continuous growth of BCCs in the lung by not only inducing macrophage infiltration but also exploiting macrophage-derived fibroblast growth factors (FGFs). Finally, we identify KRAS-PI3K-c-JUN signalling as an upstream pathway that accounts for the elevated expression of GALNT14 in lung-metastatic BCCs. Collectively, our findings uncover an unprecedented role for GALNT14 in the pulmonary metastasis of breast cancer and elucidate the underlying molecular mechanisms.

Indexed as

AnimalsBenzamidesBone Morphogenetic Protein ReceptorsBreast NeoplasmsCell Line, TumorDiaminesDioxolesFemaleGene Expression Regulation, NeoplasticGlycosylationGuanine Nucleotide Exchange FactorsHumansLungLung NeoplasmsMiceMice, Nude24-diamino-5-phenylthiazole4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideBenzamidesBone Morphogenetic Protein ReceptorsDiaminesDioxolesDMH1 compoundGuanine Nucleotide Exchange FactorsN-AcetylgalactosaminyltransferasesPolypeptide N-acetylgalactosaminyltransferasePyrazolesQuinolinesReceptors, NotchReceptors, Transforming Growth Factor betaSERGEF protein, humanThiazoles

Identifiers

PMID27982029
PMCPMC5171903
OpenAlexW2567286405

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.