Evidence map›Paper›PMID 28795305›Full record

ArticleMolecular and cellular biochemistry2018

microRNA-133a attenuates cardiomyocyte hypertrophy by targeting PKCδ and Gq.

Se-Yeon Lee, Chang Youn Lee, Onju Ham, Jae Yoon Moon, Jiyun Lee, Hyang-Hee Seo, Sunhye Shin, Sang Woo Kim, Seahyoung Lee, Soyeon Lim and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. MicroRNAs in Cardiac Hypertrophy.International journal of molecular sciences · 2019
    Review
  5. Article
  6. Article
  7. Review
  8. Article
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

11 authors at 4 institutions in 1 country.

Se-Yeon LeeBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Republic of Korea.
Chang Youn LeeDepartment of Integrated Omics for Biomedical Sciences, Yonsei University, Seoul, Republic of Korea.
Onju HamBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Republic of Korea.
Jae Yoon MoonDepartment of Cardiology, CHA Bundang Medical Center, CHA University, Seongnam, Gyeoggi-do, Republic of Korea.
Jiyun LeeBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Republic of Korea.
Hyang-Hee SeoBrain Korea 21 PLUS Project for Medical Science, Yonsei University, Seoul, Republic of Korea.
Sunhye ShinDepartment of Integrated Omics for Biomedical Sciences, Yonsei University, Seoul, Republic of Korea.
Sang Woo KimInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung, Gangwon-do, Republic of Korea.
Seahyoung LeeInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung, Gangwon-do, Republic of Korea.
Soyeon LimInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung, Gangwon-do, Republic of Korea. slim724@cku.ac.kr.
Ki-Chul HwangInstitute for Bio-Medical Convergence, College of Medicine, Catholic Kwandong University, Gangneung, Gangwon-do, Republic of Korea. kchwang@cku.ac.kr.
Yonsei University · KRCatholic Kwandong University · KRCatholic Kwandong University International St. Mary's Hospital · KRCHA University Bundang Medical Center · KR

Funding

Ministry of Health and Welfare A120478Ministry of Science, ICT and Future Planning NRF-2015M3A9E6029519
6 · The paper itself

Abstract

During the past decade, microRNAs have continuously been suggested as a promising therapeutic tool due to their beneficial effects, such as their multi-targets and multi-functions in pathologic conditions. As a pathologic phenotype is generally regulated by multiple signaling pathways, in this study we identified a microRNA regulating multiple target genes within cardiac hypertrophic signaling pathways. microRNA-133a is known to play a crucial role in cardiac hypertrophy. However, the role of microRNA-133a, which may regulate several signaling pathways in norepinephrine-induced cardiac hypertrophy via multi-targeting, has not been investigated. In the current study, we showed that microRNA-133a can protect cardiomyocyte hypertrophy against norepinephrine stimulation in neonatal rat ventricular cardiomyocytes via new targets, PKCδ and Gq, all of which are related to downstream signaling pathways of the α

Indexed as

Signal TransductionAnimalsCardiomegalyGTP-Binding Protein alpha Subunits, Gq-G11MicroRNAsMyocytes, CardiacProtein Kinase C-deltaRatsReceptor, Adenosine A1GTP-Binding Protein alpha Subunits, Gq-G11MicroRNAsMIRN133 microRNA, ratPrkcd protein, ratProtein Kinase C-deltaReceptor, Adenosine A1Cardiomyocyte hypertrophyGqmicroRNA-133aNorepinephrinePKCδ

Identifiers

PMID28795305
OpenAlexW2744301454

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.