High frequency of JAZF1-JJAZ1 gene fusion in endometrial stromal tumors with smooth muscle differentiation by interphase FISH detection.

Détails

ID Serval
serval:BIB_E57D7ABEA2A7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
High frequency of JAZF1-JJAZ1 gene fusion in endometrial stromal tumors with smooth muscle differentiation by interphase FISH detection.
Périodique
American Journal of Surgical Pathology
Auteur⸱e⸱s
Oliva E., de Leval L., Soslow R.A., Herens C.
ISSN
0147-5185[print], 0147-5185[linking]
Statut éditorial
Publié
Date de publication
2007
Volume
31
Numéro
8
Pages
1277-1284
Langue
anglais
Résumé
The most common cytogenetic alteration observed in low-grade endometrial stromal tumors (EST) is the t(7;17)(p15;q21) translocation, resulting in the fusion of the JAZF1 and JJAZ1 genes. By reverse-transcription polymerase chain reaction, the translocation has been detected overall in one-third of ESTs, but only rarely in its variants. The purpose of this study was to develop a fluorescence in situ hybridization assay for detection of this translocation using archival paraffin-embedded samples of ESTs with smooth muscle differentiation and to assess the nature of the smooth muscle component of these tumors. Representative paraffin blocks of 9 endometrial stromal nodules and 1 low-grade endometrial stromal sarcoma were collected for the study. In 1 case, the block selected also contained areas of sex cordlike differentiation. A fluorescence in situ hybridization probe set was designed to detect the t(7;17)(p15;q12) on tissue sections. Six out of 10 collected ESTs were assessable. Fusion signals were detected in 3 out of 6 cases (50%) in both the conventional endometrial stromal and the smooth muscle components of the tumors. The tumor sample with sex cordlike differentiation harbored the fusion signal in all the 3 components. Our results support the contention that the endometrial stromal and smooth muscle components of these tumors have the same origin, either from a common precursor cell with pluripotential differentiation or from endometrial stromal cells that have undergone smooth muscle metaplasia. Our results indicate that the detection of this chromosomal abnormality can be used to diagnose ESTs with smooth muscle differentiation when the smooth muscle component is predominant.
Mots-clé
Cell Transformation, Neoplastic, Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 7, DNA, Neoplasm/analysis, Endometrial Stromal Tumors/genetics, Endometrial Stromal Tumors/pathology, Female, Gene Fusion, Humans, In Situ Hybridization, Fluorescence/methods, Middle Aged, Myocytes, Smooth Muscle/pathology, Neoplasm Proteins/genetics, Neoplasm Proteins/metabolism, Sarcoma, Endometrial Stromal/genetics, Sarcoma, Endometrial Stromal/pathology, Stromal Cells/pathology, Transcription Factors/genetics, Transcription Factors/metabolism, Translocation, Genetic
Pubmed
Création de la notice
27/10/2010 9:52
Dernière modification de la notice
20/08/2019 17:08
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