نجلاء حامد ابراهيم شعلان
أستاذ مساعد
Evaluation of the expression and role of adenosine receptor and programmed death ligand-1 in bladder urothelial carcinoma
• 2024
معلومات البحث
المؤلفون
Ghada A. Abd El-Fattah, Naglaa H. Shalan, Rasha M. El Sawi
الكلمات المفتاحية
Not Available
المجلة العلمية
Not Available
الناشر
Not Available
المجلد
Not Available
العدد
Not Available
الصفحات
Not Available
publication.type
Local
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Immune-checkpoint molecules are important regulators of physiologic
inflammatory responses, and are highly effective in behavior of many cancers.
They are involved in production of antitumor immune response. This study aims to
evaluate the expression and role of both programmed death ligand-1 (PDL-1) and
adenosine receptor (A2aR) antibodies in bladder urothelial cancer.
Materials and methods
This was a retrospective study on 45 bladder urothelial cancers obtained from
archives of Pathology Department, Faculty of Medicine, Benha University and from
International Medical Center Hospital (IMC) during the period from January 2015 to
December 2019. Immunohistochemical expression of A2aR was evaluated and
compared with those of PDL-1. A2aR expression was also correlated with tumorinfiltrating
CD8+T cells. Relations to demographic data of the patients were
evaluated.
inflammatory responses, and are highly effective in behavior of many cancers.
They are involved in production of antitumor immune response. This study aims to
evaluate the expression and role of both programmed death ligand-1 (PDL-1) and
adenosine receptor (A2aR) antibodies in bladder urothelial cancer.
Materials and methods
This was a retrospective study on 45 bladder urothelial cancers obtained from
archives of Pathology Department, Faculty of Medicine, Benha University and from
International Medical Center Hospital (IMC) during the period from January 2015 to
December 2019. Immunohistochemical expression of A2aR was evaluated and
compared with those of PDL-1. A2aR expression was also correlated with tumorinfiltrating
CD8+T cells. Relations to demographic data of the patients were
evaluated.
