دورية أكاديمية

Caffeine Inhibits Migration in Glioma Cells through the ROCK-FAK Pathway

التفاصيل البيبلوغرافية
العنوان: Caffeine Inhibits Migration in Glioma Cells through the ROCK-FAK Pathway
المؤلفون: Ying Chen, Wei-Chung Chou, You-Ming Ding, Ya-Chieh Wu
المصدر: Cellular Physiology and Biochemistry, Vol 33, Iss 6, Pp 1888-1898 (2014)
بيانات النشر: Cell Physiol Biochem Press GmbH & Co KG, 2014.
سنة النشر: 2014
المجموعة: LCC:Physiology
LCC:Biochemistry
مصطلحات موضوعية: Caffeine, Rho associated kinase, Focal adhesion kinase, Glioma, Physiology, QP1-981, Biochemistry, QD415-436
الوصف: Aims: Glioma is the most malignant brain tumor that has the ability to migrate and invade the CNS. In this study, we investigated the signaling mechanism of caffeine on the migration of glioma cells. Methods: The effect of caffeine on cell migration was evaluated using Transwell and wound healing assays. The expression of the focal adhesion complex as it related to cell migration was assayed using Western blotting and immunostaining. Results: Caffeine decreased the migration of rat C6 and human U87MG glioma cells and down-regulated the expression of phosphorylated focal adhesion kinase (p-FAK) and p-paxillin. Caffeine also decreased p-FAK staining at the edge of glioma cells and disassembled actin stress fibers. Additionally, caffeine elevated expression of phosphorylated myosin light chain (p-MLC), an effect that could be blocked by Y27632, a rho-associated protein kinase (ROCK) inhibitor, but not myosin light chain kinase inhibitor, ML-7. Y27632 also inhibited the caffeine-reduced expression of p-FAK and p-paxillin as well as cell migration. Conclusion: Caffeine decreased the migration of glioma cell through the ROCK-focal adhesion complex pathway; this mechanism may be useful as part of clinical therapy in the future.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1015-8987
1421-9778
Relation: http://www.karger.com/Article/FullText/362966; https://doaj.org/toc/1015-8987; https://doaj.org/toc/1421-9778
DOI: 10.1159/000362966
URL الوصول: https://doaj.org/article/5a95d0fdd83a407891163706a89c7a8d
رقم الأكسشن: edsdoj.5a95d0fdd83a407891163706a89c7a8d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:10158987
14219778
DOI:10.1159/000362966