فراواني پايين جهش بنيان گذار 185delAG در ژن BRCA1 در بيماران ايراني مبتلا به سرطان پستان

مهدی پور, پروین ، حسینی اصل, سید سعید ، صوابی, آرزو ، حبیبی, لاله ، الوندی, احسان ، عطری, مرتضی (1385) فراواني پايين جهش بنيان گذار 185delAG در ژن BRCA1 در بيماران ايراني مبتلا به سرطان پستان. Journal of Cancer Molecules ــ 2 (3). ص.ص.123-127. شاپا 1816-0735

پیش نمایش
متنی - نسخه چاپ شده

آدرس اینترنتی رسمی : http://www.mupnet.com

عنوان انگليسي

Low Frequency of 185delAG Founder Mutation of BRCA1 Gene in Iranian Breast Cancer Patients

خلاصه انگلیسی

AIM: The mutations in two breast cancer susceptibility genes, BRCA1 and BRCA2, are frequently associated with familial breast cancer. In this study, we aimed to investigate the probable founder mutations of BRCA1 and BRCA2 genes in Iranian breast cancer patients. METHODS: The total 400 patients affected with primary breast cancer were included in this study. Mutation detection was carried out on the basis of a PCR-based amplification, and two founder mutations for BRCA1 (185delAG and 5382insC) and one for BRCA2 (6174delT) were screened and considered by pedigree analysis. RESULTS: The positive family histories of breast cancer and other malignancies were recorded in 27.5% and 52% of patient pedigrees, respectively. The most frequent occurrence of breast cancer across four generations revealed to be 50% in the 1st degree in the 3rd generation, 68.8% in the 2nd degree in the 2nd generation, and 59.5% in the 3rd degree in the 3rd generation. Only 185delAG mutation in the BRCA1 gene was found in 2/400 (0.5%) of investigated pedigrees. There were two sisters of the same family. To our interest both sisters carried 185delAG mutation in the BRCA1 gene, which had a complete penetrance. However, the mutation was observed with two different organ targeting, at almost an early age of onset (proband: 45 yr, her sister: 30 yr). CONCLUSION: Considering the importance of genetic counseling and recording, the adequate information for the pedigrees of cancer patients put forward the principle approaches in cancer clinics to facilitate early detection for preventing challenges.

نوع سند :مقاله
زبان سند : انگلیسی
نویسنده مسئول :پروین مهدی پور
نویسنده :سید سعید حسینی اصل
نویسنده :آرزو صوابی
نویسنده :لاله حبیبی
نویسنده :احسان الوندی
نویسنده :مرتضی عطری
اطلاعات اضافی :indexed: CAplus, CEPS, TEPS, Sirus, Scopus, EMBASE, Google Scholar, DOAJ
کلید واژه ها:سرطان پستان، BRCA1، BRCA2، جهش بنيان گذار، شجره نامه
کلید واژه ها (انگلیسی):Breast cancer, BRCA1, BRCA2, Founder mutation, Pedigree
موضوعات :QY آسیب شناسی بالینی
WB پزشکی عملی
WP بیماریهای زنان
بخش های دانشگاهی :دانشكده پزشكي > گروه علوم پایه > بخش ژنتیک
کد شناسایی :2539
ارائه شده توسط : دکتر سید سعید حسینی اصل
ارائه شده در تاریخ :27 خرداد 1392 07:38
آخرین تغییر :07 مهر 1393 06:37

فقط پرسنل کتابخانه صفحه کنترل اسناد

Document Downloads

More statistics for this item...