Evidence map›Paper›PMID 26967558›Full record

ArticleOncotarget2016

EBV reactivation as a target of luteolin to repress NPC tumorigenesis.

Chung-Chun Wu, Chih-Yeu Fang, Hui-Yu Hsu, Hsin-Ying Chuang, Yu-Jhen Cheng, Yen-Ju Chen, Sheng-Ping Chou, Sheng-Yen Huang, Su-Fang Lin, Yao Chang and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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
2.5field-weighted citation impact, top 9% 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, 37 citations in OpenAlex.

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  7. Luteolin Isolated fromBioMed research international · 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

12 authors at 3 institutions in 1 country.

Chung-Chun WuNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Chih-Yeu FangNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Hui-Yu HsuNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Hsin-Ying ChuangNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Yu-Jhen ChengNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Yen-Ju ChenNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Sheng-Ping ChouNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Sheng-Yen HuangNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Su-Fang LinNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
Yao ChangNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Tainan, Taiwan.
Ching-Hwa TsaiDepartment of Microbiology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Jen-Yang ChenNational Institute of Cancer Research, National Health Research Institutes, Zhunan, Taiwan.
National Health Research Institutes · TWNational Taiwan University · TWWan Fang Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nasopharyngeal carcinoma (NPC) is a malignancy derived from the epithelial cells of the nasopharynx. Although a combination of radiotherapy with chemotherapy is effective for therapy, relapse and metastasis after remission remain major causes of mortality. Epstein-Barr virus (EBV) is believed to be one of causes of NPC development. We demonstrated previously that EBV reactivation is important for the carcinogenesis of NPC. We sought, therefore, to determine whether EBV reactivation can be a target for retardation of relapse of NPC. After screening, we found luteolin is able to inhibit EBV reactivation. It inhibited EBV lytic protein expression and repressed the promoter activities of two major immediate-early genes, Zta and Rta. Furthermore, luteolin was shown to reduce genomic instability induced by recurrent EBV reactivation in NPC cells. EBV reactivation-induced NPC cell proliferation and migration, as well as matrigel invasiveness, were also repressed by luteolin treatment. Tumorigenicity in mice, induced by EBV reactivation, was decreased profoundly following luteolin administration. Together, these results suggest that inhibition of EBV reactivation is a novel approach to prevent the relapse of NPC.

Indexed as

AnimalsCarcinogenesisCarcinomaCell Line, TumorEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHumansImmediate-Early ProteinsLuteolinMiceNasopharyngeal CarcinomaNasopharyngeal NeoplasmsTrans-ActivatorsVirus ActivationBRLF1 protein, Human herpesvirus 4BZLF1 protein, Herpesvirus 4, HumanImmediate-Early ProteinsLuteolinTrans-ActivatorsEpstein-Barr virusluteolinnasopharyngeal carcinomareactivationrelapse

Identifiers

PMID26967558
PMCPMC4951347
OpenAlexW2294015830

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.