Literature DB >> 23495693

Therapeutic applications of PI3K inhibitors in cardiovascular diseases.

Alessandra Ghigo1, Fulvio Morello, Alessia Perino, Emilio Hirsch.   

Abstract

PI3Ks are signaling enzymes engaged by different types of membrane receptors and activated in cardiovascular diseases such as hypertension, atherosclerosis, thrombosis and heart failure. Studies performed on genetically modified animals have provided proof-of-concept that general or isoform-specific blockade of these enzymes can modify disease development and progression. Hence, therapeutic inhibition of PI3Ks with novel pharmacological compounds constitutes a promising area of drug development. In particular, inhibitors of PI3Ks have the potential to reduce blood pressure, restrain the development of atherosclerosis and/or stabilize atherosclerotic plaques, blunt platelet aggregation, prevent left ventricular remodeling and preserve myocardial contractility in heart failure. This review summarizes the rationale of PI3K inhibition in the most prevalent cardiovascular diseases, and the available data on the therapeutic effects of PI3K inhibitors in their preclinical models. Implications for future drug development and human therapy are also discussed.

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Year:  2013        PMID: 23495693     DOI: 10.4155/fmc.13.11

Source DB:  PubMed          Journal:  Future Med Chem        ISSN: 1756-8919            Impact factor:   3.808


  10 in total

Review 1.  Molecules in medicine mini-review: isoforms of PI3K in biology and disease.

Authors:  Bart Vanhaesebroeck; Maria A Whitehead; Roberto Piñeiro
Journal:  J Mol Med (Berl)       Date:  2015-12-10       Impact factor: 4.599

2.  Profound blockade of T cell activation requires concomitant inhibition of different class I PI3K isoforms.

Authors:  Belén Blanco; M Carmen Herrero-Sánchez; Concepción Rodríguez-Serrano; Mercedes Sánchez-Barba; M Consuelo Del Cañizo
Journal:  Immunol Res       Date:  2015-06       Impact factor: 2.829

Review 3.  Therapeutic Targeting of PDEs and PI3K in Heart Failure with Preserved Ejection Fraction (HFpEF).

Authors:  Valentina Sala; Jean Piero Margaria; Alessandra Murabito; Fulvio Morello; Alessandra Ghigo; Emilio Hirsch
Journal:  Curr Heart Fail Rep       Date:  2017-06

Review 4.  Phosphoinositide 3-Kinases as Potential Targets for Thrombosis Prevention.

Authors:  Natasha M Setiabakti; Pia Larsson; Justin R Hamilton
Journal:  Int J Mol Sci       Date:  2022-04-27       Impact factor: 6.208

5.  The phosphoinositide 3-kinase signaling pathway is involved in the control of modified low-density lipoprotein uptake by human macrophages.

Authors:  Daryn R Michael; Thomas S Davies; Lucia Laubertová; Hayley Gallagher; Dipak P Ramji
Journal:  Lipids       Date:  2015-02-08       Impact factor: 1.880

Review 6.  PI3K inhibitors in thrombosis and cardiovascular disease.

Authors:  Tom N Durrant; Ingeborg Hers
Journal:  Clin Transl Med       Date:  2020-01-31

7.  Terlipressin relieves intestinal and renal injuries induced by acute mesenteric ischemia via PI3K/Akt pathway.

Authors:  Zi-Meng Liu; Han-Jin Lai; Xiang-Dong Guan; Shi-Hong Wen; Jian-Tong Shen; Yao Nie; Ning Liu; Xu-Yu Zhang
Journal:  Int J Med Sci       Date:  2020-09-28       Impact factor: 3.738

8.  Mechanistic Insights of Qingre Jiedu Recipe Based on Network Pharmacology Approach against Heart Failure.

Authors:  Xuan Li; Mingyan Shao; Zhen Liu; Xiaoqian Sun; Lingwen Cui; Xiangning Liu; Gang Wang; Linghui Lu; Yan Wu; Chun Li
Journal:  Evid Based Complement Alternat Med       Date:  2022-01-31       Impact factor: 2.629

9.  Calycosin as a Novel PI3K Activator Reduces Inflammation and Fibrosis in Heart Failure Through AKT-IKK/STAT3 Axis.

Authors:  Xiaoping Wang; Weili Li; Yawen Zhang; Qianbin Sun; Jing Cao; NanNan Tan; Shuangjie Yang; Linghui Lu; Qian Zhang; Peng Wei; Xiao Ma; Wei Wang; Yong Wang
Journal:  Front Pharmacol       Date:  2022-02-21       Impact factor: 5.810

10.  Anti-Ischemic Effects of PIK3IP1 Are Mediated through Its Interactions with the ETA-PI3Kγ-AKT Axis.

Authors:  Jei Hyoung Park; Kyoung Jin Nho; Ji Young Lee; Yung Joon Yoo; Woo Jin Park; Chunghee Cho; Do Han Kim
Journal:  Cells       Date:  2022-07-11       Impact factor: 7.666

  10 in total

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