کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3285519 | 1209231 | 2006 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Novel Findings in Swedish Patients With MYH-Associated Polyposis: Mutation Detection and Clinical Characterization
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کلمات کلیدی
D-HPLCMYH-associated polyposisHGMDPTTRT-PCRFAPAfApBERAPCMLPAFAP, Familial Adenomatous Polyposis - آدنوماتوز پلی پوز خانوادگیadenomatous polyposis coli - آدنوماتوز پولیپوزیس کولی یا آدنوماتوس پولیپوزیس کولای protein truncation test - تست کوتاهکردن پروتئینBase-excision repair - تعمیر پایه پایهmultiplex ligation-dependent probe amplification - تقویت پروب وابسته چندگانهMYH - خیلی ممنونColorectal cancer - سرطان روده بزرگconfidence interval - فاصله اطمینانmap - نقشهreverse transcriptase polymerase chain reaction - واکنش زنجیره ای پلی مراز ترانس کریتاز معکوسHuman Gene Mutation Database - پایگاه داده جهش ژنتیکی انسانSingle nucleotide polymorphism - پلیمورفیسم تک نوکلئوتیدیattenuated familial adenomatous polyposis - پولیپوز آدنوماتوز فامیلی تضعیف شده استSNP - چندریختی تک-نوکلئوتیدCRC - کد افزونگی دورهای Denaturing high-performance liquid chromatography - کروماتوگرافی مایع با کارایی بالا
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
بیماریهای گوارشی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
Background & Aims: Biallelic mutations in the base-excision repair gene MYH have recently been associated with recessive inheritance of multiple colorectal adenomas. An investigation and characterization of MYH mutations in Swedish patients were therefore carried out. Methods: A set of 15 unrelated adenomatous polyposis coli (APC)-mutation negative patients from the Swedish Polyposis Registry was screened for germline mutations in the MYH gene. The patients were clinically characterized and compared with 43 APC-mutation positive probands diagnosed during the same period. Results: Disease-causing biallelic MYH mutations were identified in 6 patients (40%). The mean age at diagnosis was 47.8 years versus 34.1 years in APC-mutation positive patients (P = .015). Colorectal cancer at diagnosis of polyposis was present in 67% (4/6) of the patients, and all were right-sided, compared with only 19% versus 12.5% right-sided cancer in APC-mutation positive patients. Upper gastrointestinal manifestations were diagnosed in 1 of 5 compared with 23 of 27 in APC-mutation positive patients (odds ratio, 23; 95% confidence interval, 2-263; P = .0086). One family exhibited apparent dominant inheritance of colorectal adenomatous polyposis. Two new pathogenic mutations, MYH p.G175E and p.P391L, were identified. The mutations are argued to introduce profound changes in substrate-recognizing domains of the protein. Conclusions: Biallelic MYH mutations, including 2 novel mutations, were found in a substantial number of the patients with multiple colorectal adenomas who were negative for APC-mutation. The examined MYH-mutation positive patients were found to have higher risks of colorectal cancer at diagnosis, right-sided location of cancers, and a significantly lower incidence of upper gastrointestinal manifestations, compared with APC-mutation positive patients.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Clinical Gastroenterology and Hepatology - Volume 4, Issue 4, April 2006, Pages 499-506
Journal: Clinical Gastroenterology and Hepatology - Volume 4, Issue 4, April 2006, Pages 499-506
نویسندگان
Gunilla Kanter-Smoler, Jan Björk, Kaisa Fritzell, Yvonne Engwall, Birgitta Hallberg, Göran Karlsson, Henrik Grönberg, Per Karlsson, Arne Wallgren, Jan Wahlström, Rolf Hultcrantz, Margareta Nordling,