Evidence map›Paper›PMID 26544896›Full record

SynthesisOncotarget2015

GalNAc-T14 promotes metastasis through Wnt dependent HOXB9 expression in lung adenocarcinoma.

Ok-Seon Kwon, Ensel Oh, Jeong-Rak Park, Ji-Seon Lee, Gab-Yong Bae, Jae-Hyung Koo, Hyongbum Kim, Yoon L Choi, Young Soo Choi, Jhingook Kim and 1 more

Open access · diamondAbstract readMeta-Analysis
In one paragraph

Synthesis in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  12. Identification of a ModifiedJournal of oncology · 2020
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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

11 authors at 5 institutions in 1 country.

Ok-Seon KwonCollege of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
Ensel OhLaboratory of Cancer Genomics and Molecular Pathology, Samsung Biomedical Research Institute, Samsung Medical Center, Seoul, Republic of Korea.
Jeong-Rak ParkCollege of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
Ji-Seon LeeCollege of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
Gab-Yong BaeCollege of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
Jae-Hyung KooDepartment of Brain and Cognitive Sciences, DGIST, Daegyu, Republic of Korea.
Hyongbum KimDepartment of Pharmacology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yoon L ChoiDepartment of Pathology, Samsung Medical Center, Sungkyunkwan University, School of Medicine, Seoul, Republic of Korea.
Young Soo ChoiDepartment of Thoracic Surgery, Samsung Medical Center, Sungkyunkwan University, School of Medicine, Seoul, Republic of Korea.
Jhingook KimDepartment of Thoracic Surgery, Samsung Medical Center, Sungkyunkwan University, School of Medicine, Seoul, Republic of Korea.
Hyuk-Jin ChaCollege of Natural Sciences, Department of Life Sciences, Sogang University, Seoul, Republic of Korea.
Sogang University · KRSamsung Medical Center · KRSungkyunkwan University · KRDaegu Gyeongbuk Institute of Science and Technology · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While metastasis, the main cause of lung cancer-related death, has been extensively studied, the underlying molecular mechanism remains unclear. A previous clinicogenomic study revealed that expression of N-acetylgalactosaminyltransferase (GalNAc-T14), is highly inversely correlated with recurrence-free survival in those with non-small cell lung cancer (NSCLC). However, the underlying molecular mechanism(s) has not been determined. Here, we showed that GalNAc-T14 expression was positively associated with the invasive phenotype. Microarray and biochemical analyses revealed that HOXB9, the expression of which was increased in a GalNAc-T14-dependent manner, played an important role in metastasis. GalNAc-T14 increased the sensitivity of the WNT response and increased the stability of the β-catenin protein, leading to induced expression of HOXB9 and acquisition of an invasive phenotype. Pharmacological inhibition of β-catenin in GalNAc-T14-expressing cancer cells suppressed HOXB9 expression and invasion. A meta-analysis of clinical genomics data revealed that expression of GalNAc-T14 or HOXB9 was strongly correlated with reduced recurrence-free survival and increased hazard risk, suggesting that targeting β-catenin within the GalNAc-T14/WNT/HOXB9 axis may be a novel therapeutic approach to inhibit metastasis in NSCLC.

Indexed as

Cell MovementWnt Signaling PathwayAdenocarcinomaAdenocarcinoma of LungAnimalsAntineoplastic Agentsbeta CateninBridged Bicyclo Compounds, HeterocyclicCarcinoma, Non-Small-Cell LungCell Line, TumorDatabases, GeneticDisease-Free SurvivalGene Expression ProfilingHeterograftsHomeodomain ProteinsHumansAntineoplastic Agentsbeta CateninBridged Bicyclo Compounds, HeterocyclicCTNNB1 protein, humanHomeodomain ProteinsHOXB9 protein, humanICG 001N-AcetylgalactosaminyltransferasesPyrimidinonesUDP-N-acetyl-D-galactosamine polypeptide N-acetylgalactosaminyltransferase 14, humanGalNAc-T14HOXB9invasionmetastasisWNT/TCF pathway

Identifiers

PMID26544896
PMCPMC4747198
OpenAlexW2170205697

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.