دورية أكاديمية

A comprehensive review on phosphatidylinositol-3-kinase (PI3K) and its inhibitors bearing pyrazole or indazole core for cancer therapy.

التفاصيل البيبلوغرافية
العنوان: A comprehensive review on phosphatidylinositol-3-kinase (PI3K) and its inhibitors bearing pyrazole or indazole core for cancer therapy.
المؤلفون: Bastos IM; LAQV-REQUIMTE and Department of Chemistry, University of Aveiro, 3810-193, Aveiro, Portugal., Rebelo S; Institute of Biomedicine-iBiMED, Department of Medical Sciences, University of Aveiro, 3810-193, Aveiro, Portugal., Silva VLM; LAQV-REQUIMTE and Department of Chemistry, University of Aveiro, 3810-193, Aveiro, Portugal. Electronic address: verasilva@ua.pt.
المصدر: Chemico-biological interactions [Chem Biol Interact] 2024 Aug 01; Vol. 398, pp. 111073. Date of Electronic Publication: 2024 May 31.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Elsevier Country of Publication: Ireland NLM ID: 0227276 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1872-7786 (Electronic) Linking ISSN: 00092797 NLM ISO Abbreviation: Chem Biol Interact Subsets: MEDLINE
أسماء مطبوعة: Publication: Limerick : Elsevier
Original Publication: Amsterdam, Elsevier.
مواضيع طبية MeSH: Indazoles*/chemistry , Indazoles*/pharmacology , Indazoles*/therapeutic use , Pyrazoles*/chemistry , Pyrazoles*/pharmacology , Pyrazoles*/therapeutic use , Neoplasms*/drug therapy , Phosphoinositide-3 Kinase Inhibitors*/pharmacology , Phosphoinositide-3 Kinase Inhibitors*/chemistry , Phosphoinositide-3 Kinase Inhibitors*/therapeutic use , Antineoplastic Agents*/chemistry , Antineoplastic Agents*/pharmacology , Antineoplastic Agents*/therapeutic use, Humans ; Protein Kinase Inhibitors/chemistry ; Protein Kinase Inhibitors/pharmacology ; Protein Kinase Inhibitors/therapeutic use ; Animals ; Phosphatidylinositol 3-Kinases/metabolism ; Phosphatidylinositol 3-Kinases/chemistry ; Phosphatidylinositol 3-Kinase/metabolism ; Signal Transduction/drug effects
مستخلص: Cancer is a complex and multifaceted group of diseases with a high mortality rate characterized by uncontrolled proliferation of abnormal cells. Dysregulation of normal signalling pathways in cancer contributes to the different hallmarks of this disease. The signalling pathway of which phosphatidylinositol 3-kinase (PI3K) is a part is not an exception. In fact, dysregulated activation of PI3K signalling pathways can result in unbridled cellular proliferation and enhanced cell survival, thereby fostering the onset and advancement of cancer. Therefore, there is substantial interest in developing targeted therapies specifically aimed at inhibiting the PI3K enzyme and its associated pathways. Also, the therapeutic interest on pyrazoles and indazoles has been growing due to their various medicinal properties, namely, anticancer activity. Derivatives of these compounds have been studied as PI3K inhibitors, and they showed promising results. There are already some PI3K inhibitors approved by Food and Drug Administration (FDA), such as Idelalisib (Zydelig®) and Alpelisib (Piqray®). In this context, this review aims to address the importance of PI3K in cellular processes and its role in cancer. Additionally, it aims to report a comprehensive literature review of PI3K inhibitors, containing the pyrazole and indazole scaffolds, published in the last fifteen years, focusing on structure-activity relationship aspects, thus providing important insights for the design of novel and more effective PI3K inhibitors.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.)
فهرسة مساهمة: Keywords: Cancer; Indazoles; PI3K inhibitors; Phosphatidylinositol-3-kinase (PI3K); Pyrazoles; Structure-activity relationship
المشرفين على المادة: 0 (Indazoles)
0 (Pyrazoles)
0 (Phosphoinositide-3 Kinase Inhibitors)
0 (Antineoplastic Agents)
0 (Protein Kinase Inhibitors)
EC 2.7.1.- (Phosphatidylinositol 3-Kinases)
EC 2.7.1.137 (Phosphatidylinositol 3-Kinase)
تواريخ الأحداث: Date Created: 20240601 Date Completed: 20240704 Latest Revision: 20240730
رمز التحديث: 20240730
DOI: 10.1016/j.cbi.2024.111073
PMID: 38823538
قاعدة البيانات: MEDLINE
الوصف
تدمد:1872-7786
DOI:10.1016/j.cbi.2024.111073