Literature DB >> 20626398

PI3K inhibitors in cardiovascular disease.

Andreas Eisenreich1, Ursula Rauch.   

Abstract

Cardiovascular diseases, including atherosclerotic disease and its thrombotic complications are one main cause of hospitalization and mortality in the world. The family of phosphoinositide 3-kinases (PI3Ks) play an important role in the pathogenesis of cardiovascular diseases by regulating essential cellular functions, such as cell migration, translational responses, and cell survival, and thereby, modulating several essential biologic processes, such as metabolism, vascular homeostasis and thrombogenicity. PI3Ks can be divided into three classes, of which the class I-group is the best characterized. This group consists of four isoforms, named PI3Kα, β, δ, and γ. Each isoform has distinct functions under normal as well as pathophysiologic conditions. The development of several pharmacologic isoform-selective, isoform-preferring, and pan-PI3K inhibitors enlarged and potentiated the knowledge about the effect of the different PI3K isoforms on specific biologic processes as well as their role under pathophysiologic conditions. Moreover, this offered the possibility for novel therapeutic strategies targeting PI3K isoforms in cardiovascular diseases. Therefore, this review will focus on the pathophysiologic role of class I PI3Ks in cardiovascular diseases as well as on the therapeutic potential of pharmacological PI3K inhibitors for the treatment of this scourge of humanity.
© 2010 Blackwell Publishing Ltd.

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Year:  2011        PMID: 20626398     DOI: 10.1111/j.1755-5922.2010.00206.x

Source DB:  PubMed          Journal:  Cardiovasc Ther        ISSN: 1755-5914            Impact factor:   3.023


  22 in total

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3.  Kisspeptin cell-specific PI3K signaling regulates hypothalamic kisspeptin expression and participates in the regulation of female fertility.

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Review 4.  Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases.

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Review 5.  Differential regulatory functions of three classes of phosphatidylinositol and phosphoinositide 3-kinases in autophagy.

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6.  Alternatively spliced tissue factor and full-length tissue factor protect cardiomyocytes against TNF-α-induced apoptosis.

Authors:  U Boltzen; A Eisenreich; S Antoniak; A Weithaeuser; H Fechner; W Poller; H P Schultheiss; N Mackman; U Rauch
Journal:  J Mol Cell Cardiol       Date:  2012-01-31       Impact factor: 5.000

7.  Metformin modulates apoptosis and cell signaling of human podocytes under high glucose conditions.

Authors:  Sebastian Langer; Reinhold Kreutz; Andreas Eisenreich
Journal:  J Nephrol       Date:  2016-01-05       Impact factor: 3.902

Review 8.  Signaling pathways and targeted therapy for myocardial infarction.

Authors:  Qing Zhang; Lu Wang; Shiqi Wang; Hongxin Cheng; Lin Xu; Gaiqin Pei; Yang Wang; Chenying Fu; Yangfu Jiang; Chengqi He; Quan Wei
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Journal:  Arthritis Res Ther       Date:  2015-03-09       Impact factor: 5.156

10.  Differentially Expressed Circular Non-coding RNAs in Atherosclerotic Aortic Vessels and Their Potential Functions in Endothelial Injury.

Authors:  Houwei Li; Xue Liu; Na Sun; Tianshuo Wang; Jia Zhu; Shuang Yang; Xia Song; Ruishuai Wang; Xinhui Wang; Yixiu Zhao; Yan Zhang
Journal:  Front Cardiovasc Med       Date:  2021-07-07
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