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[Genomic profiling by comparative genomic hybridization: analysis of ten enucleated uveal melanoma cases].

作者信息

Abi-Ayad N, Couturier J, Devouassoux-Shisheboran M, Grange J-D, Kodjikian L, Calender A

机构信息

Service d'ophtalmologie, hôpital de la Croix-Rousse, 103, Grande rue de la Croix-Rousse, 69317 Lyon cedex 04, France.

出版信息

J Fr Ophtalmol. 2011 Jan;34(1):17-23. doi: 10.1016/j.jfo.2010.10.013. Epub 2010 Dec 8.

Abstract

AIM

To detect major chromosomal aberrations from enucleated uveal melanoma and relate them to hepatic metastasis and survival.

PATIENTS AND METHODS

Ten uveal melanomas enucleated between 2005 and 2008 in the Lyon Croix-Rousse Hospital were retrospectively analyzed using a 19 000-clone comparative genomic hybridization microarray.

RESULTS

The most frequent imbalances were the loss of chromosome 3 (8/10), gain of the 8q arm (7/10) or the entire chromosome 8 (2/10), and gain of the 6p arm (2/10). Most metastatic tumors (6/7) and all cases of death (5/5) concerned melanoma with monosomy 3 and gain of the 8q arm.

DISCUSSION AND CONCLUSION

Genome-wide array comparative genomic hybridization is a reliable tool for identifying uveal melanoma genomic imbalances. Gains of the 8q arm with monosomy 3 are frequent and are strongly associated with poor outcome. Gains of the 6p arm are rare and have a better prognosis. There is a mutually exclusive relationship between monosomy 3 and chromosome 6 abnormalities in our study. These results confirm previously published reports.

摘要

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