دورية أكاديمية

Protein tyrosine phosphatase receptor type E (PTPRE) regulates the activation of wild-type KIT and KIT mutants differently

التفاصيل البيبلوغرافية
العنوان: Protein tyrosine phosphatase receptor type E (PTPRE) regulates the activation of wild-type KIT and KIT mutants differently
المؤلفون: Shaoting Zhang, Liangying Zhang, Zongying Jiang, Yue Guo, Hui Zhao, Jianmin Sun
المصدر: Biochemistry and Biophysics Reports, Vol 26, Iss , Pp 100974- (2021)
بيانات النشر: Elsevier, 2021.
سنة النشر: 2021
المجموعة: LCC:Biology (General)
LCC:Biochemistry
مصطلحات موضوعية: KIT, PTPRE, GISTs, Mastocytosis, Mutation, Biology (General), QH301-705.5, Biochemistry, QD415-436
الوصف: Activation of receptor tyrosine kinases needs tight control by tyrosine phosphatases to keep their normal function. In this study, we investigated the regulation of activation of the type III receptor tyrosine kinase KIT by protein tyrosine phosphatase receptor type E (PTPRE). We found that PTPRE can associate with wild-type KIT and inhibit KIT activation in a dose-dependent manner, although the activation of wild-type KIT is dramatically inhibited even when PTPRE is expressed at low level. The D816V mutation of KIT is the most frequently found oncogenic mutation in mastocytosis, and we found that PTPRE can associate and inhibit the activation of KIT/D816V in a dose dependent manner, but the inhibition is much weaker compared with wild-type KIT. Similar to mastocytosis, KIT mutations are the main oncogenic mutations in gastrointestinal stromal tumors (GISTs) although GISTs carry different types of KIT mutations. We further studied the regulation of the activation of GISTs-type KIT mutants and other mastocytosis-type KIT mutants by PTPRE. Indeed, PTPRE can almost block the activation of GISTs-type KIT mutants, while the activation of mastocytosis-type KIT mutants is more resistant to the inhibition of PTPRE. Taken together, our results suggest that PTPRE can associate with KIT, and inhibit the activation of both wild-type KIT and GISTs-type KIT mutants, while the activation of mastocytosis-type KIT mutants is more resistant to PTPRE.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2405-5808
Relation: http://www.sciencedirect.com/science/article/pii/S2405580821000686; https://doaj.org/toc/2405-5808
DOI: 10.1016/j.bbrep.2021.100974
URL الوصول: https://doaj.org/article/c17f8ec197a54aadbcaf5bff2fbb87fd
رقم الأكسشن: edsdoj.17f8ec197a54aadbcaf5bff2fbb87fd
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:24055808
DOI:10.1016/j.bbrep.2021.100974