CCNE1 amplification and centrosome number abnormality in serous tubal intraepithelial carcinoma: further evidence supporting its role as a precursor of ovarian high-grade serous carcinoma

Aberration in chromosomal structure characterizes almost all cancers and has profound biological significance in tumor development. It can be facilitated by various mechanisms including overexpression of cyclin E1 and centrosome amplification. As ovarian high-grade serous carcinoma has pronounced ch...

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Veröffentlicht in:Modern pathology 2016-10, Vol.29 (10), p.1254-1261
Hauptverfasser: Kuhn, Elisabetta, Wang, Tian-Li, Doberstein, Kai, Bahadirli-Talbott, Asli, Ayhan, Ayse, Sehdev, Ann Smith, Drapkin, Ronny, Kurman, Robert J, Shih, Ie-Ming
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Sprache:eng
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Zusammenfassung:Aberration in chromosomal structure characterizes almost all cancers and has profound biological significance in tumor development. It can be facilitated by various mechanisms including overexpression of cyclin E1 and centrosome amplification. As ovarian high-grade serous carcinoma has pronounced chromosomal instability, in this study we sought to determine whether increased copy number of CCNE1 which encodes cyclin E1 and centrosome amplification (>2 copies) occurs in its putative precursor, serous tubal intraepithelial carcinoma. We found CCNE1 copy number gain/amplification in 8 (22%) of 37 serous tubal intraepithelial carcinomas and 12 (28%) of 43 high-grade serous carcinomas. There was a correlation in CCNE1 copy number between serous tubal intraepithelial carcinoma and high-grade serous carcinoma in the same patients (P
ISSN:0893-3952
1530-0285
DOI:10.1038/modpathol.2016.101