Evidence map›Paper›PMID 25238261›Full record

ArticleOncotarget2014

Interferon-stimulated gene 15 (ISG15) is a trigger for tumorigenesis and metastasis of hepatocellular carcinoma.

Chong Li, Ji Wang, Hong Zhang, Mingao Zhu, Feifei Chen, Yufeng Hu, Hudan Liu, Hong Zhu

Abstract read
In one paragraph

Article in Oncotarget, 2014. 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
–field-weighted citation impact
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.

  1. Review
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  3. International journal of molecular medicine · 2026
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9 more citing papers are in PubMed but not listed here.

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.

Chong LiDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, China. CAS Key Laboratory of Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences (CAS), Beijing, China.
Ji WangDepartment of Oncology, the Second Affiliated Hospital of Soochow University, Suzhou, China.
Hong ZhangDepartment of Oncology, the Second Affiliated Hospital of Soochow University, Suzhou, China.
Mingao ZhuDepartment of Oncology, the Second Affiliated Hospital of Soochow University, Suzhou, China.
Feifei ChenDepartment of Oncology, the Second Affiliated Hospital of Soochow University, Suzhou, China.
Yufeng HuSchool of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hudan LiuSchool of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Hong ZhuDepartment of Oncology, the First Affiliated Hospital of Soochow University, Suzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most common cancers worldwide with poor prognosis. IFN-stimulated genes 15 (ISG15) is an ubiquitin-like molecule that is strongly upregulated by type I interferons as a primary response to diverse microbial and cellular stress stimuli. However, the role of ISG15 in HCC remains unclear. In this study, we investigated the function of ISG15 during HCC progression and related mechanism using clinicopathological data, cell line and xenograft model. Our results indicated that ISG15 is highly expressed in HCC tissues and multiple HCC cell lines. ISG15 expression is significantly associated with the differentiation grade, metastatic of tumor and survival of HCC patients. However, the expression of ISG15 is not affected by HBV infection. ISG15 promotes the proliferation and migration of hepatocarcinoma cells through maintaining Survivin protein stabilization via sequestering XIAP from interacting with Survivin. Knowing down ISG15 with SiRNA inhibited the xenografted tumor growth and prolonged the lifespan of tumor-bearing mice. All these results support that ISG15 high expression is an intrinsic feature for HCC and a trigger for tumorigenesis and metastasis. ISG15 may be a prognostic biomarker and the inhibition of ISG15 could provide a therapeutic advantage for HCC patients over-expressing ISG15.

Indexed as

AdultAgedAnimalsCarcinoma, HepatocellularCell DifferentiationCell MovementCell ProliferationCell Transformation, NeoplasticCytokinesFemaleG2 Phase Cell Cycle CheckpointsHep G2 CellsHumansInhibitor of Apoptosis ProteinsKaplan-Meier EstimateLiver NeoplasmsBIRC5 protein, humanCytokinesInhibitor of Apoptosis ProteinsISG15 protein, humanSurvivinUbiquitinsXIAP protein, humanX-Linked Inhibitor of Apoptosis Protein

Identifiers

PMID25238261
PMCPMC4226694

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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.