Evidence map›Paper›PMID 30026862›Full record

ArticleTheranostics2018

Comparative profiling of analog targets: a case study on resveratrol for mouse melanoma metastasis suppression.

Xiao Chen, Wei Li, Chengchao Xu, Jie Wang, Bo Zhu, Qilai Huang, Dianhua Chen, Jianfei Sheng, Yong Zou, Yew Mun Lee and 6 more

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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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

16 authors at 3 institutions in 2 countries.

Xiao ChenThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Wei LiThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Chengchao XuDepartment of Biological Science, National University of Singapore, Singapore, 117543, Singapore.
Jie WangThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Bo ZhuThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Qilai HuangThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Dianhua ChenThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Jianfei ShengSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Yong ZouSchool of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Yew Mun LeeDepartment of Biological Science, National University of Singapore, Singapore, 117543, Singapore.
Renxiang TanThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Pingping ShenThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Yin Kwan WongDepartment of Biological Science, National University of Singapore, Singapore, 117543, Singapore.
Qingsong LinDepartment of Biological Science, National University of Singapore, Singapore, 117543, Singapore.
Jigang WangArtemisinin Research Center, China Academy of Chinese Medical Sciences, Beijing, 100700, China.
Zichun HuaThe State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, 210023, China.
Nanjing University · CNNational University of Singapore · SGSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many plant-specialized metabolites have remedial properties and provide an endless chemical resource for drug discovery. However, most of these metabolites have promiscuous binding targets in mammalian cells and elicit a series of responses that collectively change the physiology of the cells. To explore the potential of these multi-functional and multi-targeted drugs, it is critical to understand the direct relationships between their key chemical features, the corresponding binding targets and the relevant biological effects, which is a prerequisite for future drug modification and optimization.

Indexed as

Gene Expression ProfilingAnimalsAntineoplastic Agents, PhytogenicCell MovementEpigenesis, GeneticMelanomaMice, Inbred C57BLNeoplasm MetastasisResveratrolStructure-Activity RelationshipAntineoplastic Agents, PhytogenicResveratrolcancer metastasis.chemical proteomicsCPATresveratroltarget identification

Identifiers

PMID30026862
PMCPMC6037041
OpenAlexW2808295228

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.