دورية أكاديمية

Low frequency of defective mismatch repair in a population-based series of upper urothelial carcinoma

التفاصيل البيبلوغرافية
العنوان: Low frequency of defective mismatch repair in a population-based series of upper urothelial carcinoma
المؤلفون: Isfoss Björn L, Isinger Anna P, Ericson Kajsa M, Nilbert Mef C
المصدر: BMC Cancer, Vol 5, Iss 1, p 23 (2005)
بيانات النشر: BMC, 2005.
سنة النشر: 2005
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract Background Upper urothelial cancer (UUC), i.e. transitional cell carcinomas of the renal pelvis and the ureter, occur at an increased frequency in patients with hereditary nonpolyposis colorectal cancer (HNPCC). Defective mismatch repair (MMR) specifically characterizes HNPCC-associated tumors, but also occurs in subsets of some sporadic tumors, e.g. in gastrointestinal cancer and endometrial cancer. Methods We assessed the contribution of defective MMR to the development of UUC in a population-based series from the southern Swedish Cancer Registry, through microsatellite instability (MSI) analysis and immunohistochemical evaluation of expression of the MMR proteins MLH1, PMS2, MSH2, and MSH6. Results A MSI-high phenotype was identified in 9/216 (4%) successfully analyzed patients and a MSI-low phenotype in 5/216 (2%). Loss of MMR protein immunostaining was found in 11/216 (5%) tumors, and affected most commonly MSH2 and MSH6. Conclusion This population-based series indicates that somatic MMR inactivation is a minor pathway in the development of UUC, but tumors that display defective MMR are, based on the immunohistochemical expression pattern, likely to be associated with HNPCC.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1471-2407
49729535
Relation: http://www.biomedcentral.com/1471-2407/5/23; https://doaj.org/toc/1471-2407
DOI: 10.1186/1471-2407-5-23
URL الوصول: https://doaj.org/article/64c4bbbde22f49729535c6ae5e1bcf1b
رقم الأكسشن: edsdoj.64c4bbbde22f49729535c6ae5e1bcf1b
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:14712407
49729535
DOI:10.1186/1471-2407-5-23