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Identifying Novel Targetable Chromosomal Alterations in Ovarian Cancer: Using Germline Copy Numbr Variation Association Analysis

المصدر: المجلة العلمية لجامعة الملك فيصل - العلوم الأساسية والتطبيقية
الناشر: جامعة الملك فيصل
المؤلف الرئيسي: Abd Elmoneim, Hanan Mohamed (Author)
مؤلفين آخرين: Mohammed, Rehab Kamal (Co-Author) , Abd El-Meguid, Reda Fikry (Co-Author) , Tawfik, Heba Mohammed (Co-Author) , Abd Elghany, Manal Ismail (Co-Author)
المجلد/العدد: مج23, ع2
محكمة: نعم
الدولة: السعودية
التاريخ الميلادي: 2022
التاريخ الهجري: 1444
الشهر: ديسمبر
الصفحات: 12 - 19
ISSN: 1658-0311
رقم MD: 1351196
نوع المحتوى: بحوث ومقالات
اللغة: الإنجليزية
قواعد المعلومات: science
مواضيع:
كلمات المؤلف المفتاحية:
Copy Number Variations | EYA2 | Ovarian Cancer | WNK1
رابط المحتوى:
صورة الغلاف QR قانون
حفظ في:
LEADER 02632nam a22002657a 4500
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041 |a eng 
044 |b السعودية 
100 |9 684209  |a Abd Elmoneim, Hanan Mohamed  |e Author 
245 |a Identifying Novel Targetable Chromosomal Alterations in Ovarian Cancer:  |b Using Germline Copy Numbr Variation Association Analysis 
260 |b جامعة الملك فيصل  |c 2022  |m 1444  |g ديسمبر 
300 |a 12 - 19 
336 |a بحوث ومقالات  |b Article 
520 |b The heterogeneity of ovarian cancer (Ov Ca) is attributed to multiple genetic and epigenetic changes, rendering it difficult to detect the most relevant molecular alterations. Identifying copy number variations (CNVs) will be helpful in screening patients with a familial history and will ultimately facilitate early diagnosis. This work aims to determine germline CNVs that may be associated with risks for different subtypes of ovarian cancer. Using Affymetrix genome-wide human SNP 6.0 arrays, 138 germline DNA samples of non-familial ovarian cancer were analysed using Golden Helix (SVS7) software. CNVs overlapping the EYA2 (20q13.12) and WNK1 (12p13.33) genes are the top hits with a significant p-value (<0.05). Deletion is more frequent in normal and low-grade carcinomas. Commonly, ovarian cancer is copy neutral (CN2) or has copy number gains (CN3). Amplification at these locations is associated with high-grade cases, which have worse overall survival rates. A CN3 in the WNK1 gene is associated with a higher expression of mRNA. It could be concluded that ovarian cancer is associated with CN3s where the segments of DNA overlap WNK1 and EYA2. The oncogenic effect of WNK1 and EYA2 on ovaries may serve as prognostic markers for ovarian cancer. 
653 |a الأورام الخبيثة  |a سرطان المبيض  |a علم الوراثة  |a الأحماض النووية  |a التداخلات الجينية 
692 |b Copy Number Variations  |b EYA2  |b Ovarian Cancer  |b WNK1 
700 |9 716358  |a Mohammed, Rehab Kamal  |e Co-Author 
700 |9 716361  |a Abd El-Meguid, Reda Fikry  |e Co-Author 
700 |9 716363  |a Tawfik, Heba Mohammed  |e Co-Author 
700 |9 716365  |a Abd Elghany, Manal Ismail  |e Co-Author 
773 |c 003  |e Scientific Journal of King Faisal University - Basic and Applied Sciences  |f almajalat aleilmiat lijamieat almalik fysl. aleulum al'asasiat waltatbiqia  |l 002  |m مج23, ع2  |o 0184  |s المجلة العلمية لجامعة الملك فيصل - العلوم الأساسية والتطبيقية  |v 023  |x 1658-0311 
856 |u 0184-023-002-003.pdf 
930 |d y  |p y  |q n 
995 |a science 
999 |c 1351196  |d 1351196 

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