Evidence map›Paper›PMID 28272394›Full record

ArticleScientific reports2017

Amigo2-upregulation in Tumour Cells Facilitates Their Attachment to Liver Endothelial Cells Resulting in Liver Metastases.

Yusuke Kanda, Mitsuhiko Osaki, Kunishige Onuma, Ayana Sonoda, Masanobu Kobayashi, Junichi Hamada, Garth L Nicolson, Takahiro Ochiya, Futoshi Okada

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

30 citing papers in PubMed, 51 citations in OpenAlex.

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  14. Adhesion molecule Amigo2 is involved in the fasciculation process of the fasciculus retroflexus.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
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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

9 authors at 3 institutions in 2 countries.

Yusuke KandaDivision of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Mitsuhiko OsakiDivision of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Kunishige OnumaDivision of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Ayana SonodaDivision of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Masanobu KobayashiHealth Sciences University of Hokkaido, School of Nursing and Social Services, Ishikari-Tobetsu, Japan.
Junichi HamadaHealth Sciences University of Hokkaido, School of Nursing and Social Services, Ishikari-Tobetsu, Japan.
Garth L NicolsonDepartment of Molecular Pathology, The Institute for Molecular Medicine, South Laguna Beach, CA, USA.
Takahiro OchiyaDivision of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tsukiji, Chuo-ku, Tokyo, Japan.
Futoshi OkadaDivision of Pathological Biochemistry, Tottori University Faculty of Medicine, Yonago, Japan.
Tottori University · JPHealth Sciences University of Hokkaido · JPInstitute for Molecular Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since liver metastasis is the main cause of death in cancer patients, we attempted to identify the driver gene involved. QRsP-11 fibrosarcoma cells were injected into the spleens of syngeneic mice to isolate tumour sub-populations that colonize the liver. Cells from liver metastatic nodules were established and subsequently injected intrasplenically for selection. After 12 cycles, the cell subline LV12 was obtained. Intravenous injection of LV12 cells produced more liver metastases than QRsP-11 cells, whereas the incidence of lung metastases was similar to that of QRsP-11 cells. LV12 cells adhered to liver-derived but not to lung-derived endothelial cells. DNA chip analysis showed that amphoterin-induced gene and open reading frame 2 (Amigo2) was overexpressed in LV12 cells. siRNA-mediated knockdown of Amigo2 expression in LV12 cells attenuated liver endothelial cell adhesion. Ex vivo imaging showed that suppression of Amigo2 in luciferase-expressing LV12 cells reduced attachment/metastasis to liver to the same level as that observed with QRsP-11 cells. Forced expression of Amigo2 in QRsP-11 cells increased liver endothelial cell adhesion and liver metastasis. Additionally, Amigo2 expression in human cancers was higher in liver metastatic lesions than in primary lesions. Thus, Amigo2 regulated tumour cell adhesion to liver endothelial cells and formation of liver metastases.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBiomarkers, TumorCell AdhesionCell Line, TumorColonic NeoplasmsDisease Models, AnimalEndothelial CellsFemaleHumansLiver NeoplasmsMembrane ProteinsMiceNerve Tissue ProteinsPrognosisStomach NeoplasmsAmigo2 protein, mouseBiomarkers, TumorMembrane ProteinsNerve Tissue Proteins

Identifiers

PMID28272394
PMCPMC5341090
OpenAlexW2592199419

What OpenQuestion holds

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LicenceCC BY
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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.