Evidence map›Paper›PMID 34102609›Full record

ArticleAging2021

Inhibition of CDK9 attenuates atherosclerosis by inhibiting inflammation and phenotypic switching of vascular smooth muscle cells.

Shushi Huang, Wu Luo, Gaojun Wu, Qirui Shen, Zaishou Zhuang, Daona Yang, Jinfu Qian, Xiang Hu, Yan Cai, Nipon Chattipakorn and 2 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Aging, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Shushi HuangChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Wu LuoChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Gaojun WuDepartment of Cardiology, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Qirui ShenChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Zaishou ZhuangAffiliated Cangnan Hospital, Wenzhou Medical University, Cangnan, Zhejiang 325000, China.
Daona YangAffiliated Cangnan Hospital, Wenzhou Medical University, Cangnan, Zhejiang 325000, China.
Jinfu QianChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Xiang HuDepartment of Endocrinology, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Yan CaiAffiliated Cangnan Hospital, Wenzhou Medical University, Cangnan, Zhejiang 325000, China.
Nipon ChattipakornCardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Weijian HuangDepartment of Cardiology, The First Affiliated Hospital, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Guang LiangChemical Biology Research Center, School of Pharmaceutical Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China.
Wenzhou Medical University · CNFirst Affiliated Hospital of Wenzhou Medical University · CNChiang Mai University · THHangzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have demonstrated a key role of vascular smooth muscle cell (VSMC) dysfunction in atherosclerosis. Cyclin-dependent kinases 9 (CDK9), a potential biomarker of atherosclerosis, was significantly increased in coronary artery disease patient serum and played an important role in inflammatory diseases. This study was to explore the pharmacological role of CDK9 inhibition in attenuating atherosclerosis.

methodsA small-molecule CDK9 inhibitor, LDC000067, was utilized to treat the high fat diet (HFD)-fed ApoE

resultsThe results showed that inflammation and phenotypic switching of VSMCs were observed in HFD-induced atherosclerosis in ApoE

conclusionThese results indicate that inhibition of CDK9 may be a novel therapeutic target for the prevention of atherosclerosis.

Indexed as

AnimalsApolipoproteins EAtherosclerosisCyclin-Dependent Kinase 9Diet, High-FatHumansInflammationLipoproteins, LDLMaleMiceMuscle, Smooth, VascularMyocytes, Smooth MuscleNF-kappa BPhenotypeProtein Kinase InhibitorsRNA, Small InterferingApolipoproteins ECDK9 protein, humanCyclin-Dependent Kinase 9Lipoproteins, LDLNF-kappa Boxidized low density lipoproteinProtein Kinase InhibitorsRNA, Small InterferingatherosclerosisCDK9inflammationpharmacological inhibitionphenotypic switchingvascular smooth muscle cells

Identifiers

PMID34102609
PMCPMC8221363
OpenAlexW3169436064

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.