Evidence map›Paper›PMID 33934437›Full record

ArticleCancer science2021

CEBPγ facilitates lamellipodia formation and cancer cell migration through CERS6 upregulation.

Hanxiao Shi, Atsuko Niimi, Toshiyuki Takeuchi, Kazuya Shiogama, Yasuyoshi Mizutani, Taisuke Kajino, Kenichi Inada, Tetsunari Hase, Takahiro Hatta, Hirofumi Shibata and 8 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

15 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
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  4. Mechanisms of GPM6A in Malignant Tumors.Cancer reports (Hoboken, N.J.) · 2025
    Review
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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

18 authors at 6 institutions in 1 country.

Hanxiao ShiDepartment of Molecular Oncology, School of Medicine, Fujita Health University, Toyoake, Japan.
Atsuko NiimiDepartment of Molecular Oncology, School of Medicine, Fujita Health University, Toyoake, Japan.
Toshiyuki TakeuchiDepartment of Molecular Oncology, School of Medicine, Fujita Health University, Toyoake, Japan.
Kazuya ShiogamaDepartment of Morphology and Cell Function, School of Medical Sciences, Fujita Health University, Toyoake, Japan.
Yasuyoshi MizutaniDepartment of Molecular Oncology, School of Medicine, Fujita Health University, Toyoake, Japan.
Taisuke KajinoDivision of Molecular Diagnostics, Aichi Cancer Center Research Institute, Nagoya, Japan.
Kenichi InadaDiagnostic Pathology, Bantane Hospital, Fujita Health University, Toyoake, Japan.
Tetsunari HaseDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takahiro HattaDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Hirofumi ShibataDepartment of Respiratory Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takayuki FukuiDepartment of Thoracic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Toyofumi Fengshi Chen-YoshikawaDepartment of Thoracic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Kazuki NaganoDepartment of Pathophysiological Laboratory Science, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Takashi MurateDepartment of Pathophysiological Laboratory Science, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Yoshiyuki KawamotoCollege of Life and Health Sciences, Chubu University, Kasugai, Japan.
Shuta TomidaCenter for Comprehensive Genomic Medicine, Okayama University Hospital, Okayama, Japan.
Takashi TakahashiDivision of Molecular Carcinogenesis, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0003-0615-7001
Motoshi SuzukiDepartment of Molecular Oncology, School of Medicine, Fujita Health University, Toyoake, Japan.ORCID https://orcid.org/0000-0003-0682-5006
Fujita Health University · JPNagoya University · JPAichi Cancer Center · JPChubu University · JPFujita Health University Hospital · JPOkayama University Hospital · JP

Funding

Aichi Cancer Research FoundationJapan Society for the Promotion of Science 18H02698Japan Society for the Promotion of Science 18K07030Japan Society for the Promotion of Science 18K07193
6 · The paper itself

Abstract

Ceramide synthase 6 (CERS6) promotes lung cancer metastasis by stimulating cancer cell migration. To examine the underlying mechanisms, we performed luciferase analysis of the CERS6 promoter region and identified the Y-box as a cis-acting element. As a parallel analysis of database records for 149 non-small-cell lung cancer (NSCLC) cancer patients, we screened for trans-acting factors with an expression level showing a correlation with CERS6 expression. Among the candidates noted, silencing of either CCAAT enhancer-binding protein γ (CEBPγ) or Y-box binding protein 1 (YBX1) reduced the CERS6 expression level. Following knockdown, CEBPγ and YBX1 were found to be independently associated with reductions in ceramide-dependent lamellipodia formation as well as migration activity, while only CEBPγ may have induced CERS6 expression through specific binding to the Y-box. The mRNA expression levels of CERS6, CEBPγ, and YBX1 were positively correlated with adenocarcinoma invasiveness. YBX1 expression was observed in all 20 examined clinical lung cancer specimens, while 6 of those showed a staining pattern similar to that of CERS6. The present findings suggest promotion of lung cancer migration by possible involvement of the transcription factors CEBPγ and YBX1.

Indexed as

Cell MovementPseudopodiaCarcinoma, Non-Small-Cell LungCCAAT-Enhancer-Binding ProteinsCell Line, TumorHumansLung NeoplasmsMembrane ProteinsNeoplasm InvasivenessPromoter Regions, Geneticrac1 GTP-Binding ProteinRNA, MessengerSphingosine N-AcyltransferaseTranscriptional ActivationUp-RegulationY-Box-Binding Protein 1CCAAT-enhancer-binding protein-gammaCCAAT-Enhancer-Binding ProteinsCERS6 protein, humanMembrane Proteinsrac1 GTP-Binding ProteinRAC1 protein, humanRNA, MessengerSphingosine N-AcyltransferaseY-Box-Binding Protein 1YBX1 protein, humanCEBPγCERS6lung cancermetastasisYBX1

Identifiers

PMID33934437
PMCPMC8253294
OpenAlexW3157186015

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.