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Loss of expression of DNA mismatch repair proteins is rare in pancreatic and small intestinal neuroendocrine tumors.错配修复蛋白缺失在胰腺和小肠神经内分泌肿瘤中很少见。
Arch Pathol Lab Med. 2011 Dec;135(12):1539-44. doi: 10.5858/arpa.2010-0560-OA.
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Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.由于TACSTD1基因3'外显子缺失导致的林奇综合征家族中MSH2基因的可遗传体细胞甲基化和失活。
Nat Genet. 2009 Jan;41(1):112-7. doi: 10.1038/ng.283. Epub 2008 Dec 21.
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Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).林奇综合征（遗传性非息肉病性结直肠癌）的筛查
N Engl J Med. 2005 May 5;352(18):1851-60. doi: 10.1056/NEJMoa043146.
4
Frequent promoter methylation of tumor-related genes in sporadic and men2-associated pheochromocytomas.散发性和与MEN2相关的嗜铬细胞瘤中肿瘤相关基因的频繁启动子甲基化
Exp Clin Endocrinol Diabetes. 2005 Jan;113(1):1-7. doi: 10.1055/s-2004-830522.
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Microsatellite instability and gene mutations in transforming growth factor-beta type II receptor are absent in small bowel carcinoid tumors.小肠类癌肿瘤不存在微卫星不稳定性和转化生长因子-βⅡ型受体基因突变。
Cancer. 2005 Jan 15;103(2):229-36. doi: 10.1002/cncr.20750.
6
MSH2 mutation carriers are at higher risk of cancer than MLH1 mutation carriers: a study of hereditary nonpolyposis colorectal cancer families.与错配修复基因1（MLH1）突变携带者相比，错配修复基因2（MSH2）突变携带者患癌风险更高：一项遗传性非息肉病性结直肠癌家族研究。
J Clin Oncol. 2001 Oct 15;19(20):4074-80. doi: 10.1200/JCO.2001.19.20.4074.

HNPCC-associated pheochromocytoma: expanding the tumor spectrum.

作者信息

Riff Brian P, Katona Bryson W, Wilkerson Myra, Nathanson Katherine L, Metz David C

机构信息

Division of Gastroenterology University of Pennsylvania Philadelphia, PA Division of Pathology and Laboratory Medicine Geisinger Health System Wilkes-Barre, PA Division of Medical Genetics University of Pennsylvania Philadelphia, PA Division of Gastroenterology University of Pennsylvania Philadelphia, PA

出版信息

Pancreas. 2015 May;44(4):676-8. doi: 10.1097/MPA.0000000000000311.

DOI:10.1097/MPA.0000000000000311
PMID:25872134
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4399001/
Abstract
摘要