Widespread Mismatch Repair Protein Expression in Canine Cutaneous Mast Cell Tumors

被引:6
作者
Munday, J. S. [1 ]
French, A. F. [2 ]
Gibson, I. R. [3 ]
Gwynne, K. [4 ]
机构
[1] Massey Univ, Inst Vet Anim & Biomed Sci, Palmerston North, New Zealand
[2] New Zealand Vet Pathol Ltd, Palmerston North, New Zealand
[3] New Zealand Vet Pathol Ltd, Hamilton, New Zealand
[4] Medlab Cent, Palmerston North, New Zealand
关键词
Canines; HNPCC; Lynch syndrome mast cell tumor; MMR; Muir-Torre syndrome; neoplasia; skin; NONPOLYPOSIS COLORECTAL-CANCER; MICROSATELLITE INSTABILITY; C-KIT; MALIGNANT-MELANOMA; SKIN-CANCER; HMSH2; MICE; FEATURES; HNPCC; GENE;
D O I
10.1354/vp.46-2-227
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Cutaneous mast cell tumors (MCTs) are common canine neoplasms. Some dog breeds more frequently develop MCTs, suggesting a genetically mediated predisposition. In humans, the most common inherited cancer predisposition is caused by germline defects in the mismatch repair (MMR) genes. To investigate whether inherited defects in the MMR genes predispose some dogs to MCT development, MMR expression in 22 MCTs from young and predisposed breed dogs was compared with MMR expression in 22 MCTs from old dogs of non-MCT-predisposed breeds. MMR expression was investigated immunohistochemically using antibodies against MLH1, MSH2, and MSH6. Mast cells within all MCTs expressed MLH1, MSH2, and MSH6. There were no significant differences in the intensity of immunoreactivity or the percentage of cells expressing MMR proteins between MCTs from the 2 groups of dogs. There were no significant differences in MMR protein expression between grade II and grade III MCTs. These results do not support the hypothesis that inherited MMR defects predispose some dogs to MCT development.
引用
收藏
页码:227 / 232
页数:6
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