دورية أكاديمية

Blocking the PD-1/PD-L1 pathway in glioma: a potential new treatment strategy

التفاصيل البيبلوغرافية
العنوان: Blocking the PD-1/PD-L1 pathway in glioma: a potential new treatment strategy
المؤلفون: Song Xue, Man Hu, Veena Iyer, Jinming Yu
المصدر: Journal of Hematology & Oncology, Vol 10, Iss 1, Pp 1-10 (2017)
بيانات النشر: BMC, 2017.
سنة النشر: 2017
المجموعة: LCC:Diseases of the blood and blood-forming organs
LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: PD-1, PD-L1, Expression, Immunosuppressive, Treatment, Glioma, Diseases of the blood and blood-forming organs, RC633-647.5, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract Gliomas are the most common type of primary brain tumor in adults. High-grade neoplasms are associated with poor prognoses, whereas low-grade neoplasms are associated with 5-year overall survival rates of approximately 85%. Despite considerable progress in treatment modalities, the outcomes remain dismal. As is the case with many other tumors, gliomas express or secrete several immunosuppressive molecules that regulate immune cell function. Programmed death-ligand 1 (PD-L1) is a coinhibitory ligand that is predominantly expressed by tumor cells. The binding of PD-L1 to its receptor PD-1 has been demonstrated to induce an immune escape mechanism and to play a critical role in tumor initiation and development. Encouraging results following the blockade of the PD-1/PD-L1 pathway have validated PD-L1 or PD-1 as a target for cancer immunotherapy. Studies have reported that the PD-1/PD-L1 pathway plays a key role in glioma progression and in the efficacy of immunotherapies. Thus, progress in research into PD-L1 will enable us to develop a more effective and individualized immunotherapeutic strategy for gliomas. In this paper, we review PD-L1 expression, PD-L1-mediated immunosuppressive mechanisms, and the clinical applications of PD-1/PD-L1 inhibitors in gliomas. Potential treatment strategies and the challenges that may occur during the clinical development of these agents for gliomas are also reviewed.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1756-8722
Relation: http://link.springer.com/article/10.1186/s13045-017-0455-6; https://doaj.org/toc/1756-8722
DOI: 10.1186/s13045-017-0455-6
URL الوصول: https://doaj.org/article/ed2e4b0ca2f74836856bd839bd765798
رقم الأكسشن: edsdoj.2e4b0ca2f74836856bd839bd765798
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:17568722
DOI:10.1186/s13045-017-0455-6