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Immuno-histochemical evaluation of2WT13 expression in Astrocytic tumors and its relationship with cellular proliferation index 2Ki673/ Eman Mohamed Momtaz Moussa ; Supervised Ahmed Mahmoud Abdelaziz , Rasha Ahmed Khairy , Somia Abdulatif Mahmoud Soliman

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Eman Mohamed Momtaz Moussa , 2020Description: 128 P. : charts , facimiles ; 25cmOther title:
  • دراسة كيميائية هستومناعية للتعبيرعن "دابليو تى وان" فى الاورام النجمية و علاقته بمؤشر التكاثر للخلايا "كى اى67" [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pathology Summary: Background:Astrocytic gliomas are the most common glial neoplasms, accounting for 60% of them. Although Wilms{u2019} tumor gene (WT1) was initially known as a tumor marker in Wilms{u2019} tumor, its mutation has recently been detected in gliomas. Expanding data indicate that WT1 mutation plays a contributive role in gliomagenesis and is overexpressed in most glioblastomas.Lately, clinical trials of cancer immunotherapy targeting WT1 protein have shown promising results in glioblastomas mostly in resistant cases, recommending that WT1 can be a possible target for immunotherapy in high-grade gliomas. Objectives:The goal of the current study was to further specify WT1 expression across different histological grades of astrocytomas to increase its diagnostic lucidity and reliability in routine diagnostic work,besides its correlation with Ki-67 labeling index and the clinico-pathological parameters of the tumors as well. Material and methods:This was a retrospective study on 46 cases of astrocytomas.Immunohistochemical expression of WT1& Ki-67 was assessed in the tumor cells. Results:Forty-six astrocytomas were assessed for WT1 by immunohistochemistry. WT1 immunoexpression was detected in all astrocytomas (100%). WT1 score correlated with the tumor histological grades (P < 0.001) with higher score in higher grade. WT1 score showed a significant correlation with K-67 labeling index as well(P < 0.001). WT1 score was valuable in differentiating high- and low-grade astrocytomas
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.27.M.Sc.2020.Em.I (Browse shelf(Opens below)) Not for loan 01010110082627000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.27.M.Sc.2020.Em.I (Browse shelf(Opens below)) 82627.CD Not for loan 01020110082627000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Pathology

Background:Astrocytic gliomas are the most common glial neoplasms, accounting for 60% of them. Although Wilms{u2019} tumor gene (WT1) was initially known as a tumor marker in Wilms{u2019} tumor, its mutation has recently been detected in gliomas. Expanding data indicate that WT1 mutation plays a contributive role in gliomagenesis and is overexpressed in most glioblastomas.Lately, clinical trials of cancer immunotherapy targeting WT1 protein have shown promising results in glioblastomas mostly in resistant cases, recommending that WT1 can be a possible target for immunotherapy in high-grade gliomas. Objectives:The goal of the current study was to further specify WT1 expression across different histological grades of astrocytomas to increase its diagnostic lucidity and reliability in routine diagnostic work,besides its correlation with Ki-67 labeling index and the clinico-pathological parameters of the tumors as well. Material and methods:This was a retrospective study on 46 cases of astrocytomas.Immunohistochemical expression of WT1& Ki-67 was assessed in the tumor cells. Results:Forty-six astrocytomas were assessed for WT1 by immunohistochemistry. WT1 immunoexpression was detected in all astrocytomas (100%). WT1 score correlated with the tumor histological grades (P < 0.001) with higher score in higher grade. WT1 score showed a significant correlation with K-67 labeling index as well(P < 0.001). WT1 score was valuable in differentiating high- and low-grade astrocytomas

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