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العنوان
Utilizing Biotechnological tools to study Galectins and EMT Gene Expression in Breast Cancer Patients \
المؤلف
Abd-Elfatah, Mahmoud Moustafa.
هيئة الاعداد
باحث / محمود مصطفى عبد الفتاح السيد
مشرف / نجوى حسن على حسن
مشرف / إيمان جودة فرحات
مشرف / رهام حسان جمعة حلوه
تاريخ النشر
2024.
عدد الصفحات
242 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
علم الحيوان والطب البيطري
تاريخ الإجازة
1/1/2024
مكان الإجازة
جامعة عين شمس - كلية العلوم - علم الحيوان
الفهرس
Only 14 pages are availabe for public view

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from 242

Abstract

Introduction:
Breast cancer is a prevalent malignant disease characterized by abnormal cell growth in the breast tissue. It affects women of various age groups from adolescence to post-menopause. Galectins, which belong to a family of carbohydrate-binding proteins, are well-known for their multifaceted and profound influence on a wide range of essential cellular functions and biological processes. Investigating how galectins influence breast cancer progression may offer insights for prognostic and targeted therapeutic advancements.
Patients and Methods:
We designed and manufactured custom kits for RNA extraction and qRT-PCR, which we used to analyze gene expression of galectins and EMT markers in 40 breast cancer patients, present in National Cancer Institute (NCI), Cairo University (CU).
Results:
Our successful development of custom kits for this study, using triphasic phenol reagent and purified Taq polymerase and MMLV enzymes, played a pivotal role in facilitating the investigation. These kits served as an essential tool in our research, allowed us to conduct a comprehensive investigation on galectins gene expression and EMT markers in samples of breast cancer patients. The results of our study showed a consistent downregulation in gene expression across all the studied galectin genes, except for LGALS-7, which exhibited a remarkable upregulation of 47.5%. We identified a strong correlation between the gene expression of individual members within the galectin family. Furthermore, our investigation showed a parallel downregulation in EMT markers. Importantly, the study showed correlation between the gene expression of galectins and EMT markers, suggesting a compelling relation between these two molecular aspects.
Conclusion:
Our custom kits enabled us to make a gene profiling study. Galectins mostly showed downregulation, except LGALS-7 which was upregulated. We also observed reduced EMT markers and a strong galectin-EMT association.