Evidence map›Paper›PMID 30765861›Full record

ArticleOncogene2019

Interferon-stimulated gene 15 modulates cell migration by interacting with Rac1 and contributes to lymph node metastasis of oral squamous cell carcinoma cells.

Yu-Lin Chen, Wan-Lin Wu, Chuan-Wei Jang, Yi-Chen Yen, Ssu-Han Wang, Fang-Yu Tsai, Ying-Ying Shen, Ya-Wen Chen

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

25 citing papers in PubMed, 41 citations in OpenAlex.

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  11. STING-dependent interferon signatures restrict osteoclast differentiation and bone loss in mice.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

8 authors at 1 institution in 1 country.

Yu-Lin ChenNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Wan-Lin WuNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Chuan-Wei JangNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Yi-Chen YenNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Ssu-Han WangNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Fang-Yu TsaiNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan.
Ying-Ying ShenPathology Core Laboratory, National Health Research Institutes, Miaoli, Taiwan.
Ya-Wen ChenNational Institute of Cancer Research, National Health Research Institutes, Miaoli, Taiwan. ywc@nhri.org.tw.ORCID http://orcid.org/0000-0002-6080-8859
National Health Research Institutes · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In an effort to understand the underlying mechanisms of lymph node metastasis in oral squamous cell carcinoma (OSCC), through in vivo selection, LN1-1 cells were previously established from OEC-M1 cells and showed enhanced lymphangiogenesis and lymphatic metastasis capabilities. In the current study, we use a stable isotope labeling with amino acids in cell culture (SILAC) and liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based proteomic platform to compare LN1-1 to OEC-M1 cells. Interferon-stimulated gene 15 (ISG15) was found highly expressed in LN1-1 cells. Immunohistochemical analysis and meta-analysis of publicly available microarray datasets revealed that the ISG15 level was increased in human OSCC tissues and associated with poor disease outcome. Knockdown of ISG15 had minimal effects on tumor growth but did decrease tumor lymphangiogenesis and lymphatic metastasis of LN1-1 cells. Consistent with the in vivo assay, ISG15 knockdown did not impair cell growth but diminished cell migration, invasion, and transendothelial migration in vitro. ISG15-induced cell migration was independent of ISGylation and associated with membrane protrusion. Ectopic expression of ISG15 increased Rac1 activity and knockdown of Rac1 impaired ISG15-enhanced migration. Furthermore, Rac1 colocalized with ISG15 to a region of membrane protrusion and ISG15 coimmunoprecipitated with Rac1, especially with the Rac1-GDP form. Importantly, as shown by proximity ligation assays, ISG15 and Rac1 physically interacted with each other. Our results indicated that ISG15 affects cell migration by interacting with Rac1 and regulating Rac1 activity and contributes to lymphatic metastasis in OSCC.

Indexed as

Lymphatic MetastasisAnimalsCarcinoma, Squamous CellCell Line, TumorCell MovementCell ProliferationCytokinesGene Expression Regulation, NeoplasticHumansKeratinocytesMaleMiceMice, Inbred BALB CMice, NudeMouth NeoplasmsNeoplasm InvasivenessCytokinesISG15 protein, humanrac1 GTP-Binding ProteinRAC1 protein, humanUbiquitins

Identifiers

PMID30765861
OpenAlexW2911400017

What OpenQuestion holds

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Read underepoch 390

Registered trials

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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.