Evidence map›Paper›PMID 39520538›Full record

ArticleCellular and molecular life sciences : CMLS2024

Dapagliflozin targets SGLT2/SIRT1 signaling to attenuate the osteogenic transdifferentiation of vascular smooth muscle cells.

Long Li, Huimin Liu, Quanyou Chai, Junyi Wei, Yuqiao Qin, Jingyao Yang, He Liu, Jia Qi, Chunling Guo, Zhaoyang Lu

Abstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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

10 authors.

Long Li *Institute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China.
Huimin Liu *Institute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China. flysharon@zju.edu.cn.
Quanyou Chai *Institute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China.
Junyi WeiDepartment of Hematology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Yuqiao QinDepartment of Hematology, The Second Hospital of Shanxi Medical University, Taiyuan, China.
Jingyao YangDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, 030001, China.
He LiuInstitute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China.
Jia QiDepartment of Pharmacy, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Chunling GuoInstitute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China. guochunling2018@d.sxmu.edu.cn.
Zhaoyang LuInstitute of Immunology and Department of Cardiology at Sir Run-Run Shaw Hospital, Zhejiang University School of Medicine, 866 Yuhangtang Road, Hangzhou, Zhejiang, 310058, China. luzhaoyang@zju.edu.cn.ORCID http://orcid.org/0000-0003-3367-2674

Funding

National Natural Science Foundation of China 81302768National Natural Science Foundation of China 81800171National Natural Science Foundation of China 81900275National Natural Science Foundation of China 82270435
6 · The paper itself

Abstract

Vascular calcification is a complication that is frequently encountered in patients affected by atherosclerosis, diabetes, and chronic kidney disease (CKD), and that is characterized by the osteogenic transdifferentiation of vascular smooth muscle cells (VSMCs). At present, there remains a pressing lack of any effective therapies that can treat this condition. The sodium-glucose transporter 2 (SGLT2) inhibitor dapagliflozin (DAPA) has shown beneficial effects in cardiovascular disease. The role of this inhibitor in the context of vascular calcification, however, remains largely uncharacterized. Our findings revealed that DAPA treatment was sufficient to alleviate in vitro and in vivo osteogenic transdifferentiation and vascular calcification. Interestingly, our study demonstrated that DAPA exerts its anti-calcification effects on VSMCs by directly targeting SGLT2, with the overexpression of SGLT2 being sufficient to attenuate these beneficial effects. DAPA was also able to limit the glucose levels and NAD

Indexed as

Benzhydryl CompoundsCell TransdifferentiationGlucosidesMuscle, Smooth, VascularMyocytes, Smooth MuscleOsteogenesisSignal TransductionSirtuin 1Sodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsVascular CalcificationAnimalsCells, CulturedGlucoseHumansMaleBenzhydryl CompoundsdapagliflozinGlucoseGlucosidesSirtuin 1Sodium-Glucose Transporter 2Sodium-Glucose Transporter 2 InhibitorsCalorie restrictionDapagliflozinSGLT2SIRT1Vascular calcification

Identifiers

PMID39520538
PMCPMC11550308

What OpenQuestion holds

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Registered trials

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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.