دورية أكاديمية

Research Status of the Orphan G Protein Coupled Receptor 158 and Future Perspectives

التفاصيل البيبلوغرافية
العنوان: Research Status of the Orphan G Protein Coupled Receptor 158 and Future Perspectives
المؤلفون: Xianan Fu, Shoupeng Wei, Tao Wang, Hengxin Fan, Ying Zhang, Clive Da Costa, Sebastian Brandner, Guang Yang, Yihang Pan, Yulong He, Ningning Li
المصدر: Cells, Vol 11, Iss 8, p 1334 (2022)
بيانات النشر: MDPI AG, 2022.
سنة النشر: 2022
المجموعة: LCC:Cytology
مصطلحات موضوعية: GPCR, GPR158, cancer, psychological disorders, Cytology, QH573-671
الوصف: G-protein-coupled receptors (GPCRs) remain one of the most successful targets for therapeutic drugs approved by the US Food and Drug Administration (FDA). Many novel orphan GPCRs have been identified by human genome sequencing and considered as putative targets for refractory diseases. Of note, a series of studies have been carried out involving GPCR 158 (or GPR158) since its identification in 2005, predominantly focusing on the characterization of its roles in the progression of cancer and mental illness. However, advances towards an in-depth understanding of the biological mechanism(s) involved for clinical application of GPR158 are lacking. In this paper, we clarify the origin of the GPR158 evolution in different species and summarize the relationship between GPR158 and different diseases towards potential drug target identification, through an analysis of the sequences and substructures of GPR158. Further, we discuss how recent studies set about unraveling the fundamental features and principles, followed by future perspectives and thoughts, which may lead to prospective therapies involving GPR158.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2073-4409
Relation: https://www.mdpi.com/2073-4409/11/8/1334; https://doaj.org/toc/2073-4409
DOI: 10.3390/cells11081334
URL الوصول: https://doaj.org/article/17d2f3b12d1e4596a56853faaccebb14
رقم الأكسشن: edsdoj.17d2f3b12d1e4596a56853faaccebb14
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20734409
DOI:10.3390/cells11081334