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العنوان
The prognostic significance of FOXC1 and MAP7 genes expression in acute myeloid leukemia cases among Egyptian population /
الناشر
Safa Mohamed Nabawy ,
المؤلف
Safa Mohamed Nabawy
هيئة الاعداد
باحث / Safa Mohamed Nabawy
مشرف / Lobna Ahmed Abdelazim Refaat
مشرف / Reham Ahmed Rashed
مشرف / Hussam Mohamed Naser Aldin
تاريخ النشر
2020
عدد الصفحات
144 P. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
علم الأورام
تاريخ الإجازة
12/4/2020
مكان الإجازة
جامعة القاهرة - معهد الأورام القومى - Clinical Pathology
الفهرس
Only 14 pages are availabe for public view

from 167

from 167

Abstract

Forkhead box (FOX) proteins are a group of transcriptional factors implicated in different cellular functions such as differentiation, proliferation and senescence. In addition to its role in physiological processes, deregulation of FOX proteins is also involved in the development and progression of tumors raising the possibility that FOX proteins could be used as diagnostic markers and therapeutic targets for cancer. Microtubules are a major component of the eukaryotic cytoskeleton that Microtubules play important roles in virtually every cellular process, such as cell division, cell motility, intracellular organization and trafficking of organelles. Misregulation of such MAPs (Microtubule associated proteins) could interfere with chromosome segregation or cell polarity and potentially contribute to oncogenesis. Aim of the work: To study the diagnostic and prognostic significance of MAP7 and FOXC1 expression in newly diagnosed AML.Methods: Prospective study on 80 AML patients treated at medical oncology departments. FOXC1 and MAP 7genes expression was evaluated by real time RT-PCR using taqman primer probe assay All patients received current standard of care treatment for AML at NCI, Cairo University, Egypt. Results: The median age of the AML patients was {uF0BB}42 years ranging between 18 -65 years. We found that FOXC1was highly expressedin 65/80 (81.3%) of AML patients and high FOXC1 expression was associated with intermediate cytogenetic risk 32(59.3%). The most frequent FAB subtype among high FOXC1 expressers was M2 followed by M4 and M1. High FOXC1 was significantly associated with worse OS (P=0.041), PFS (P=0.024)