Literature DB >> 30557630

KIT as a therapeutic target for non-oncological diseases.

Asuncion Martinez-Anton1, Delphine Gras1, Arnaud Bourdin2, Patrice Dubreuil3, Pascal Chanez4.   

Abstract

KIT is a receptor tyrosine kinase that after binding to its ligand stem cell factor activates signaling cascades linked to biological processes such as proliferation, differentiation, migration and cell survival. Based on studies performed on SCF and/or KIT mutant animals that presented anemia, sterility, and/or pigmentation disorders, KIT signaling was mainly considered to be involved in the regulation of hematopoiesis, gametogenesis, and melanogenesis. More recently, novel animal models and ameliorated cellular and molecular techniques have led to the discovery of a widen repertoire of tissue compartments and functions that are being modulated by KIT. This is the case for the lung, heart, nervous system, gastrointestinal tract, pancreas, kidney, liver, and bone. For this reason, the tyrosine kinase inhibitors that were originally developed for the treatment of hemato-oncological diseases are being currently investigated for the treatment of non-oncological disorders such as asthma, rheumatoid arthritis, and alzheimer's disease, among others. The beneficial effects of some of these tyrosine kinase inhibitors have been proven to depend on KIT inhibition. This review will focus on KIT expression and regulation in healthy and pathologic conditions other than cancer. Moreover, advances in the development of anti-KIT therapies, including tyrosine kinase inhibitors, and their application will be discussed.
Copyright © 2018. Published by Elsevier Inc.

Entities:  

Keywords:  KIT; Non-oncological diseases; SCF; Tyrosine kinase inhibitors

Mesh:

Substances:

Year:  2018        PMID: 30557630     DOI: 10.1016/j.pharmthera.2018.12.008

Source DB:  PubMed          Journal:  Pharmacol Ther        ISSN: 0163-7258            Impact factor:   12.310


  6 in total

1.  'Youthful' phenotype of c-Kit+ cardiac fibroblasts.

Authors:  Fareheh Firouzi; Oscar Echeagaray; Carolina Esquer; Natalie A Gude; Mark A Sussman
Journal:  Cell Mol Life Sci       Date:  2022-07-16       Impact factor: 9.207

2.  Differentiation of fetal hematopoietic stem cells requires ARID4B to restrict autocrine KITLG/KIT-Src signaling.

Authors:  In-Chi Young; Bogang Wu; Jaclyn Andricovich; Sung-Ting Chuang; Rong Li; Alexandros Tzatsos; Ray-Chang Wu; Mei-Yi Wu
Journal:  Cell Rep       Date:  2021-11-23       Impact factor: 9.423

Review 3.  Mastocytosis and Mast Cell Activation Disorders: Clearing the Air.

Authors:  Clayton Webster Jackson; Cristina Marie Pratt; Chase Preston Rupprecht; Debendra Pattanaik; Guha Krishnaswamy
Journal:  Int J Mol Sci       Date:  2021-10-19       Impact factor: 5.923

4.  CircRNA-3302 promotes endothelial-to-mesenchymal transition via sponging miR-135b-5p to enhance KIT expression in Kawasaki disease.

Authors:  Chao Ni; Huixian Qiu; Shuchi Zhang; Qihao Zhang; Ruiyin Zhang; Jinhui Zhou; Jinshun Zhu; Chao Niu; Rongzhou Wu; Chuxiao Shao; Abdullah Al Mamun; Bo Han; Maoping Chu; Chang Jia
Journal:  Cell Death Discov       Date:  2022-06-29

5.  Association of extracellular vesicle inflammatory proteins and mortality.

Authors:  Nicole Noren Hooten; Stephanie Torres; Nicolle A Mode; Alan B Zonderman; Paritosh Ghosh; Ngozi Ezike; Michele K Evans
Journal:  Sci Rep       Date:  2022-08-18       Impact factor: 4.996

Review 6.  Overview of current targeted therapy in gallbladder cancer.

Authors:  Xiaoling Song; Yunping Hu; Yongsheng Li; Rong Shao; Fatao Liu; Yingbin Liu
Journal:  Signal Transduct Target Ther       Date:  2020-10-07
  6 in total

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