- 作者：Minoru Takata ; Takefumi Suzuki ; Shinichi Ansai ; Tetsunori Kimura ; Fumiaki Shirasaki ; Naohito Hatta and Toshiaki Saida
- 刊名：Journal of Dermatological Science
- 出版年：2005
- 期刊代码：153_09231811
- 类别：med
- 出版时间：2005
- 卷：40
- 期：1
- 页码：51-57
- 文件大小：506 K
Summary
Background:The histopathology of melanocytic tumors sometimes presents diagnostic problems. Applicable parameters other than routine pathology are needed.Objective:
We assessed the feasibility of multiplex ligation-dependent probe amplification (MLPA), a novel PCR-based genome profiling method, in the classification of melanocytic tumors.
Method:
We extracted DNA from paraffin-embedded tissue sections of 24 primary melanomas, 14 Spitz nevi and 17 common melanocytic nevi. We analyzed the copy number gains or losses of a total of 76 genes spanning almost all chromosome arms using commercially available MLPA kits.
Results:
Although four melanocytic nevi and three Spitz nevi did not yield sufficient DNA for reliable analysis due to small tumor size, the MLPA analysis was feasible and applicable to the remaining 88%of samples. We found multiple genetic aberrations in primary melanomas. The total number of aberrations in each tumor ranged from 1 to 32 (average, 12.04). All but two melanomas showed aberrations at more than three genetic loci. Seventeen (70.8%) of the 24 melanomas showed a copy number loss of either the CDKN2A or CDKN2B gene on chromosome 9p21. All the Spitz nevi and 7 (50%) of 14 common melanocytic nevi had copy number changes at one or two gene loci (average, 1.04). The receiver operator characteristic curve analysis showed that the threshold value of copy number aberrations corresponding to 98%specificity for melanoma was 2.42 and the sensitivity using this threshold value was 92.5%.
Conclusions:
MLPA could be used as an adjunctive diagnostic tool for melanocytic tumors.