Evidence map›Paper›PMID 32374060›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

H19/TET1 axis promotes TGF-β signaling linked to endothelial-to-mesenchymal transition.

Tiefeng Cao, Ying Jiang, Da Li, Xiaoli Sun, Yuanyuan Zhang, Lingfeng Qin, George Tellides, Hugh S Taylor, Yingqun Huang

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

27 citing papers in PubMed, 41 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

9 authors at 4 institutions in 2 countries.

Tiefeng CaoDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Ying JiangDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Da LiDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Xiaoli SunDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Yuanyuan ZhangDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Lingfeng QinDepartment of Surgery, Yale University School of Medicine, New Haven, CT, USA.
George TellidesDepartment of Surgery, Yale University School of Medicine, New Haven, CT, USA.
Hugh S TaylorDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Yingqun HuangDepartment of Obstetrics, Gynecology, & Reproductive Sciences, Yale University School of Medicine, New Haven, CT, USA.
Yale University · USAffiliated Hospital of Nantong University · CNChina Medical University · CNJiangsu Province Hospital · CN

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
H19 Long Noncoding RNA in Hepatic Gluconeogenesis RegulationR01DK119386 · NIDDK · YALE UNIVERSITY · PI HUANG, YINGQUN · 2018 to 2020
$1.2M
NCATS NIH HHS UL1 TR001863NIDDK NIH HHS R01 DK119386
6 · The paper itself

Abstract

While emerging evidence suggests the link between endothelial activation of TGF-β signaling, induction of endothelial-to-mesenchymal transition (EndMT), and cardiovascular disease (CVD), the molecular underpinning of this connection remains enigmatic. Here, we report aberrant expression of H19 lncRNA and TET1 in endothelial cells (ECs) of human atherosclerotic coronary arteries. Using primary human umbilical vein endothelial cells (HUVECs) and aortic endothelial cells (HAoECs) we show that TNF-α, a known risk factor for endothelial dysfunction and CVD, induces H19 expression which in turn activates TGF-β signaling and EndMT via a TET1-dependent epigenetic mechanism. We also show that H19 regulates TET1 expression at the posttranscriptional level. Further, we provide evidence that this H19/TET1-mediated regulation of TGF-β signaling and EndMT occurs in mouse pulmonary microvascular ECs in vivo under hyperglycemic conditions. We propose that endothelial activation of the H19/TET1 axis may play an important role in EndMT and perhaps CVD.

Indexed as

AnimalsCells, CulturedCoronary VesselsEpithelial-Mesenchymal TransitionHumansHuman Umbilical Vein Endothelial CellsMiceMice, Inbred C57BLMice, KnockoutMixed Function OxygenasesProto-Oncogene ProteinsRNA, Long NoncodingRNA Processing, Post-TranscriptionalSignal TransductionTransforming Growth Factor betaH19 long non-coding RNAMixed Function OxygenasesProto-Oncogene ProteinsRNA, Long NoncodingTET1 protein, humanTransforming Growth Factor betaatherosclerosiscardiovascularEndMTepigeneticLncRNA

Identifiers

PMID32374060
PMCPMC7364839
OpenAlexW3022030418

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.