Evidence map›Paper›PMID 28767652›Full record

ArticlePloS one2017

Comparative studies of three cholesteryl ester transfer proteins and their interactions with known inhibitors.

Ziyun Wang, Manabu Niimi, Qianzhi Ding, Zhenming Liu, Ling Wang, Jifeng Zhang, Jun Xu, Jianglin Fan

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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 5 institutions in 3 countries.

Ziyun WangDepartment of Molecular Pathology, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Manabu NiimiDepartment of Molecular Pathology, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.
Qianzhi DingSchool of Pharmaceutical Sciences & Institute of Human Virology, Sun Yat-Sen University, Guangzhou, China.
Zhenming LiuState Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, China.
Ling WangSchool of Pharmaceutical Sciences & Institute of Human Virology, Sun Yat-Sen University, Guangzhou, China.
Jifeng ZhangCardiovascular Center, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, United States of America.
Jun XuSchool of Pharmaceutical Sciences & Institute of Human Virology, Sun Yat-Sen University, Guangzhou, China.
Jianglin FanDepartment of Molecular Pathology, Interdisciplinary Graduate School of Medicine, University of Yamanashi, Yamanashi, Japan.ORCID http://orcid.org/0000-0002-1737-6130
Sun Yat-sen University · CNPeking University · CNUniversity of Michigan · USUniversity of Yamanashi · JPXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates bidirectional transfers of cholesteryl esters and triglycerides between low-density lipoproteins and high-density lipoproteins (HDL). Because low levels of plasma CETP are associated with increased plasma HDL-cholesterol, therapeutic inhibition of CETP activity is considered an attractive strategy for elevating plasma HDL-cholesterol, thereby hoping to reduce the risk of cardiovascular disease. Interestingly, only a few laboratory animals, such as rabbits, guinea pigs, and hamsters, have plasma CETP activity, whereas mice and rats do not. It is not known whether all CETPs in these laboratory animals are functionally similar to human CETP. In the current study, we compared plasma CETP activity and characterized the plasma lipoprotein profiles of these animals. Furthermore, we studied the three CETP molecular structures, physicochemical characteristics, and binding properties with known CETP inhibitors in silico. Our results showed that rabbits exhibited higher CETP activity than guinea pigs and hamsters, while these animals had different lipoprotein profiles. CETP inhibitors can inhibit rabbit and hamster CETP activity in a similar manner to human CETP. Analysis of CETP molecules in silico revealed that rabbit and hamster CETP showed many features that are similar to human CETP. These results provide novel insights into understanding CETP functions and molecular properties.

Indexed as

AnimalsAnticholesteremic AgentsBenzodiazepinesBinding SitesCholesterolCholesterol Ester Transfer ProteinsCholesterol, HDLCricetinaeGuinea PigsLipoproteins, LDLMaleMolecular Dynamics SimulationOxazolidinonesPhylogenyProtein Structure, TertiaryRabbitsanacetrapibAnticholesteremic AgentsBenzodiazepinesCholesterolCholesterol Ester Transfer ProteinsCholesterol, HDLevacetrapibLipoproteins, LDLOxazolidinonesTriglycerides

Identifiers

PMID28767652
PMCPMC5540280
OpenAlexW2741548739

What OpenQuestion holds

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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.