Evidence map›Paper›PMID 31636070›Full record

ArticleAntimicrobial agents and chemotherapy2019

Anti-inflammatory Compound Shows Therapeutic Safety and Efficacy against Flavivirus Infection.

Fu-Kai Chuang, Shih-Ming Huang, Ching-Len Liao, An-Rong Lee, Shu-Pei Lien, Yu-Lung Chiu, Tsung-Hsien Chang, Pei-Ling Tsai, Ren-Jye Lin, Chih-Chin Shih and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 18 citations in OpenAlex.

  1. 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

13 authors at 3 institutions in 1 country.

Fu-Kai ChuangPenghu Branch of Tri-Service General Hospital, Penghu, Taiwan, Republic of China.
Shih-Ming HuangDepartment of Biochemistry, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Ching-Len LiaoNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli, Taiwan, Republic of China.
An-Rong LeeSchool of Pharmacy, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Shu-Pei LienNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli, Taiwan, Republic of China.
Yu-Lung ChiuSchool of Public Health, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Tsung-Hsien ChangDepartment of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Pei-Ling TsaiNational Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli, Taiwan, Republic of China.
Ren-Jye LinNational Mosquito-Borne Diseases Control Research Center, National Health Research Institute, Miaoli, Taiwan, Republic of China.
Chih-Chin ShihDepartment of Pharmacology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Yi-Jing TsaiDepartment of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan, Republic of China.
Gu-Jiun LinDepartment of Biology and Anatomy, National Defense Medical Center, Taipei, Taiwan, Republic of China.ORCID 0000-0003-4302-8196
Li-Chen YenDepartment of Microbiology and Immunology, National Defense Medical Center, Taipei, Taiwan, Republic of China yenlichen1030@gmail.com.
National Defense Medical Center · TWNational Health Research Institutes · TWTri-Service General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flaviviruses comprise several medically important viruses, including Japanese encephalitis virus, West Nile virus, dengue virus (DENV), yellow fever virus, and Zika virus (ZIKV). A large outbreak of DENV and ZIKV occurred recently, leading to many cases of illness and death. However, despite decades of effort, we have no clinically specific therapeutic drugs against DENV and ZIKV. Previous studies showed that inflammatory responses play a critical role in dengue and Zika virus pathogenesis. Thus, in this study, we examined a series of novel anti-inflammatory compounds and found that treatment with compound 2d could dose dependently reduce viral protein expression and viral progeny production in HEK-293 and Raw264.7 cells infected with four serotypes of DENV and ZIKV. In addition, considering medication safety, compound 2d could not suppress cyclooxygenase-1 (COX-1) enzymatic activities and thus could prevent the side effect of bleeding. Moreover, compound 2d significantly inhibited COX-2 enzymatic activities and prostaglandin E

Indexed as

AnimalsAnti-Inflammatory AgentsAntiviral AgentsCelecoxibCyclooxygenase 1Cyclooxygenase 2 InhibitorsDengueDengue VirusDisease Models, AnimalDose-Response Relationship, DrugHEK293 CellsHumansMiceMice, 129 StrainRAW 264.7 CellsSafetyAnti-Inflammatory AgentsAntiviral AgentsCelecoxibCyclooxygenase 1Cyclooxygenase 2 Inhibitorsanti-inflammatory compoundantiviral agentsdengue virusflavivirus

Identifiers

PMID31636070
PMCPMC7187576
OpenAlexW2981569901

What OpenQuestion holds

Textmetadata
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.