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Histopathologic study and immunohistochemical expression of WT1 protein in different types and grades of astrocytic tumors / Nashwah Samir M. Abdalmoneim Alhariry ; Supervised Badawia Bayoumy Ibrahim , Mustafa M. Sami Salem , Amal Ahmad M. Hareedy

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nashwah Samir M. Abdalmoneim Alhariry , 2015Description: 116 P. : charts , facsimiles ; 25cmOther title:
  • دراسه هستوباثولوجيه والتعبيرالهستوكيميائى المناعى للبروتين دبليوتى1 في مختلف أنواع ودرجات الاورام النجميه [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pathology Summary: Background:Wilms{u2019} tumour gene product (WT1) is an embryonic zinc-finger transcription factor, which was originally identified as a tumor suppressor gene and documented as a target for gene therapy of many solid tumors including astrocytic tumors. Aim of work: The aim of this study is the assessment of immunohistochemical expression of WT1 protein, in different histologic types and grades of astrocytic tumors. WT1 protein expression will be correlated with various clinical data (such as age, sex).Material and Methods: The material of this study consisted of 80 paraffin blocks of astrocytoma cases collected from Nasser Institute for Research and Treatment from January 2012 toDecember 2013.Results: WT1 was expressed in (25/28) grade I astrocytomas, all grade II astrocytomas (14/14), (13/16) grade III astrocytomas and (21/22) grade IV with highly significant relationship (P-value<0.001) between grade I and grade IV, grade III and grade IV. Expression was the highest in older ages (significantp-value = 0.034),in male cases (insignificantp-value = 0.298) and in areas of perivascular proliferation and the astrocytic tumors subtypes (gemistocytic astrocytoma, pleomorphic xanthoastrocytoma, protoplasmic astrocytoma and glioblastoma). Conclusion:Many factors affect the expression of WT1 in astrocytomas, rather than the tumor grade, which include tumor vasculature, patient age and the tumor subtype. Recommendations:Further studies are recommended for assessment of WT1 expression in astrocytomas in relation to other brain tumors for detection of its specificity and sensitivity for astrocytic tumors and correlation of WT1 expression with the extent of tumor vasculature and each of astrocytoma histologic subtype and patients{u2019} age.
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.27.Ph.D.2015.Na.H (Browse shelf(Opens below)) Not for loan 01010110068633000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.27.Ph.D.2015.Na.H (Browse shelf(Opens below)) 68633.CD Not for loan 01020110068633000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Pathology

Background:Wilms{u2019} tumour gene product (WT1) is an embryonic zinc-finger transcription factor, which was originally identified as a tumor suppressor gene and documented as a target for gene therapy of many solid tumors including astrocytic tumors. Aim of work: The aim of this study is the assessment of immunohistochemical expression of WT1 protein, in different histologic types and grades of astrocytic tumors. WT1 protein expression will be correlated with various clinical data (such as age, sex).Material and Methods: The material of this study consisted of 80 paraffin blocks of astrocytoma cases collected from Nasser Institute for Research and Treatment from January 2012 toDecember 2013.Results: WT1 was expressed in (25/28) grade I astrocytomas, all grade II astrocytomas (14/14), (13/16) grade III astrocytomas and (21/22) grade IV with highly significant relationship (P-value<0.001) between grade I and grade IV, grade III and grade IV. Expression was the highest in older ages (significantp-value = 0.034),in male cases (insignificantp-value = 0.298) and in areas of perivascular proliferation and the astrocytic tumors subtypes (gemistocytic astrocytoma, pleomorphic xanthoastrocytoma, protoplasmic astrocytoma and glioblastoma). Conclusion:Many factors affect the expression of WT1 in astrocytomas, rather than the tumor grade, which include tumor vasculature, patient age and the tumor subtype. Recommendations:Further studies are recommended for assessment of WT1 expression in astrocytomas in relation to other brain tumors for detection of its specificity and sensitivity for astrocytic tumors and correlation of WT1 expression with the extent of tumor vasculature and each of astrocytoma histologic subtype and patients{u2019} age.

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