Evidence map›Paper›PMID 35936222›Full record

ArticleOxidative medicine and cellular longevity2022

Silencing TUFM Inhibits Development of Monocrotaline-Induced Pulmonary Hypertension by Regulating Mitochondrial Autophagy via AMPK/mTOR Signal Pathway.

Ruyuan Wei, Xin Lv, Changcun Fang, Chuanzhen Liu, Zengshan Ma, Kai Liu

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Mitophagy in cardiovascular diseases: a literature review.Cardiovascular diagnosis and therapy · 2026
    Review
  2. Article
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  11. Review
  12. Article
  13. The role and mechanism of AMPK in pulmonary hypertension.Therapeutic advances in respiratory disease
    Review
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

6 authors at 1 institution in 1 country.

Ruyuan WeiCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0001-8966-7757
Xin LvCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0002-7919-5589
Changcun FangCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0003-4184-1562
Chuanzhen LiuCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0003-1426-5045
Zengshan MaCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0002-3631-4795
Kai LiuCheeloo College of Medicine, Shandong University, Jinan City, Shandong Province, 250012, China.ORCID https://orcid.org/0000-0002-4475-0730
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary arterial hypertension (PAH) is an extremely malignant cardiovascular disease which mainly involves the uncontrollable proliferation of the pulmonary arterial smooth muscular cells (PASMCs). Recent studies have confirmed that mitochondria play an important role in the pathogenesis of pulmonary hypertension through sensing cell hypoxia, energy metabolism conversion, and apoptosis. As a mitochondrial membrane protein, TUFM has been regarded to be related to mitochondrial autophagy (mitophagy), apoptosis, and oxidative stress. Considering these factors are closely associated with the pathogenesis of PAH, we hypothesize that TUFM might play a role in the development of PAH. Our preliminary examination has showed TUFM mainly expressed in the PASMCs, and the subsequent test indicated an increased TUFM expression in the SMCs of pulmonary arteriole in monocrotaline- (MCT-) induced PAH rat model compared with the normal rat. The TUFM knockdown (Sh-TUFM) or overexpressed (OE-TUFM) rats were used to establish PAH by treating with MCT. A notable lower pulmonary arterial systolic pressure together with slightly morphological changes of pulmonary arteriole was observed in the Sh-TUFM group compared with the single MCT-induced PAH group. Increased levels of P62 and Bax and reduced LC3II/I, BECN1, and Bcl2 were detected in the Sh-TUFM group, while the expressions of these proteins in the OE-TUFM group were contrast to the results of the Sh-TUFM group. To elucidate the possible mechanism underlying biological effect of TUFM in PAH, PASMCs were treated with silence or overexpression of TUFM and then exposed to hypoxia condition. An obviously high levels of P62 and Bax along with a decreased LC3 II/I, BECN1, ULK1, Atg12, Atg13, and Bcl2 levels were noticed in cells with silence of TUFM. Moreover, the phosphorylated AMPK and mTOR which was well known in mitophagy modulating vary by the alternation of TUFM. These observations suggested that TUFM silence inhibits the development of MCT-induced PAH via AMPK/mTOR pathway.

Indexed as

Hypertension, PulmonaryPulmonary Arterial HypertensionAMP-Activated Protein KinasesAnimalsAutophagybcl-2-Associated X ProteinCell ProliferationDisease Models, AnimalMitochondriaMonocrotalineMyocytes, Smooth MuscleRatsRats, Sprague-DawleySignal TransductionTOR Serine-Threonine KinasesAMP-Activated Protein Kinasesbcl-2-Associated X ProteinMonocrotalinemTOR protein, ratTOR Serine-Threonine Kinases

Identifiers

PMID35936222
PMCPMC9348918
OpenAlexW4288067285

What Socratic holds

Textmetadata
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 Socratic graph.