Genetic Polymorphisms of Glutathione S-transferase GSTM1 and GSTT1 among Acute Myeloid Leukemic Patients, National Cancer Institute, University of Gezira, Sudan (2018)
تعدد أشكال الوراثة من GSTT1 و GSTM1 كعامل خطر لزيادة حدوث سرطان الدم النخاعي الحاد - المعهد القومى للسرطان جامعة الجزيرة - السودان (2018)
Salah Alzaki, Ozaz Yagoub , مصطفى إبراهيم عباس البشير
كلية علوم المختبرات الطبية-جامعة الجزيرة · السودان
الموضوعات
طب
الملخص
Leukaemias in general population result from interaction between genetic and environmental factors and time. The interplay of xenobiotics exposure, endogenous physiology, and genetic variability of multiple loci may facilitate knowledge about leukaemia etiology and the identification of individuals who are at increased risk of developing leukaemias. This is hospital based case control study aimed to determine the genetics polymorphism of GSTT1 and GSTM1 as risk factor to develop acute myeloid leukemia. The sample were collected from diagnosed patients who attended the National Cancer Institute –Gezira state during the period of (2017 -2018). The study included: 20 cases and 20 healthy volunteers matched for sex and age whose were selected according to inclusion and exclusion criteria .Three ml of blood was collected in EDTA tubes, then the complete blood count (CBC) was done by automated hematology analyzer and followed by DNA extraction and then amplification by PCR using predesigned primers the products visualized by using gel documentation system. Data analysis was done by statistical package for social science computer program. The study results showed the frequency of null, GSTM1 and GSTT1 deletion genotype was 55%, 20% and 15%, respectively in AML patient where as 30%, 15% and 45% respectively in controls. No statistical significant differences in GSTM1 deletion, GSTT1 deletion and null genotypes between AML patients as compared to controls (p-value 0.202, 0.189 and 0.582) retrospectively .Also there was no statistical significant among different age groups and genders (p.value 0.704and 0.269) retrospectively. The CBC parameters show highly statistical significant difference between the cases and controls (p.value 0.00) except the WBCs show no statistical significant difference between cases and control (p.value 0.064). The Study recommended that use advance technique for future screening and involving other GST family among different age groups, and use this polymorphism as prognostic marker and chemotherapy response marker. The study recommended that use advance technique for future screening and involving other GST family among different age groups.
روابط وملفات
التعريف والنوع
- رقم الوثيقة
- eb6a49fb-3647-4520-9982-0b6d275577fb
- رقم العقد
- 0
- نوع الوسائط
- Crawler
- نوع المحتوى
- الرسائل العلمية
- صيغة المصدر
- رسائل ماجيستير
- نوع الملف
- pdf image
- أسماء الملفات
- eb6a49fb-3647-4520-9982-0b6d275577fb_1.pdf
بيانات النشر
- ترجمة العنوان
- تعدد أشكال الوراثة من GSTT1 و GSTM1 كعامل خطر لزيادة حدوث سرطان الدم النخاعي الحاد - المعهد القومى للسرطان جامعة الجزيرة - السودان (2018)
- ألقاب المؤلفين
- [{"name_ar":" Salah Alzaki","title_ar":"اشراف","title_en":"Supervision"},{"name_ar":"Ozaz Yagoub ","title_ar":"اشراف","title_en":"Supervision"},{"name_ar":"مصطفى إبراهيم عباس البشير ","title_ar":"اعداد","title_en":"Preparation"}]
- اللغة
- English
المصدر والدورية
- اسم المصدر
- Genetic Polymorphisms of Glutathione S-transferase GSTM1 and GSTT1 among Acute Myeloid Leukemic Patients, National Cancer Institute, University of Gezira, Sudan (2018)
المحتوى والصفحات
- عدد الصفحات
- 0
إشراف وإعداد
- الإشراف
- Salah Alzaki, Ozaz Yagoub
- الإعداد
- مصطفى إبراهيم عباس البشير
الاقتباسات الببليوغرافية
APA
MLA