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Ex-vivo modeling of leukemic stem cell niche : Sub - classifying CD34⁺ population according to quiescence / Nesreen Hamdi Mahmoud ; Supervised Iman Ahmed Maher Mansour , Nadia Ibrahim Sewilam

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Nesreen Hamdi Mahmoud , 2014Description: 145 P. : charts , facsimiles ; 25cmOther title:
  • علي حسب درجة سكونها CD 34⁺التمثيل الخارجي للبيئة المحيطة بالخلايا الجذعية في حالات اللوكيميا الحادة لتقسيم الخلايا الجذعية اللوكيميا الحادة [Added title page title]
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Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology Summary: Acute myeloid leukemia is a paradigm of cancer stem (or leukemia initiating) cells. Stem cell niche acts as a sanctuary for the stem cells that allow their survival, self-renewal and regulated proliferation. In parallel with leukemogenic events in the hematopoietic system, the niche is converted into an environment with dominant signals that favor cell proliferation and growth. Using ex-vivo culture, the present study simulated the bone marrow niche. Mononuclear cells from bone marrow aspirates of AML cases and controls were co-cultured on confluent mesenchymal stem cell layer. We estimated the percent of cells in G0 phase of the cell cycle and percentage of CD34⁺38- cells in the 3 layers of the ex-vivo culture. In AML cases, the distribution of the CD34⁺38- cells, revealed a significant difference between the 3 layers (p < 0.001), with a significantly lower percent in layer 3. A statistically significant difference between layer 3 of the cases and of the controls (p < 0.026), was also detected. No statistically significant difference in mean percentage of quiescent cells (PI⁺ Ki-67- ) was found on comparing the percentage of G0 cells in layer 1 and 2 of cases to those of control subjects. It was concluded that mesenchymal cell interaction with leukemic cells resulted in an altered distribution of the CD34⁺38- cell compartment when compared to normal but did not affect the cycling status of the cells
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.Ph.D.2014.Ne.E (Browse shelf(Opens below)) Not for loan 01010110065115000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.07.Ph.D.2014.Ne.E (Browse shelf(Opens below)) 65115.CD Not for loan 01020110065115000

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

Acute myeloid leukemia is a paradigm of cancer stem (or leukemia initiating) cells. Stem cell niche acts as a sanctuary for the stem cells that allow their survival, self-renewal and regulated proliferation. In parallel with leukemogenic events in the hematopoietic system, the niche is converted into an environment with dominant signals that favor cell proliferation and growth. Using ex-vivo culture, the present study simulated the bone marrow niche. Mononuclear cells from bone marrow aspirates of AML cases and controls were co-cultured on confluent mesenchymal stem cell layer. We estimated the percent of cells in G0 phase of the cell cycle and percentage of CD34⁺38- cells in the 3 layers of the ex-vivo culture. In AML cases, the distribution of the CD34⁺38- cells, revealed a significant difference between the 3 layers (p < 0.001), with a significantly lower percent in layer 3. A statistically significant difference between layer 3 of the cases and of the controls (p < 0.026), was also detected. No statistically significant difference in mean percentage of quiescent cells (PI⁺ Ki-67- ) was found on comparing the percentage of G0 cells in layer 1 and 2 of cases to those of control subjects. It was concluded that mesenchymal cell interaction with leukemic cells resulted in an altered distribution of the CD34⁺38- cell compartment when compared to normal but did not affect the cycling status of the cells

Issued also as CD

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