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在卵巢间质瘤的纤维瘤-卵泡膜瘤组中,4号、9号和12号染色体失衡较为常见。

Imbalances of chromosomes 4, 9, and 12 are recurrent in the thecoma-fibroma group of ovarian stromal tumors.

作者信息

Streblow Renae C, Dafferner Alicia J, Nelson Marilu, Fletcher Mavis, West William W, Stevens Rachel K, Gatalica Zoran, Novak Deborah, Bridge Julia A

机构信息

Departments of Pathology and Microbiology, University of Nebraska Medical Center, 983135 Nebraska Medical Center, Omaha, NE 68198-3135, USA.

出版信息

Cancer Genet Cytogenet. 2007 Oct 15;178(2):135-40. doi: 10.1016/j.cancergencyto.2007.07.009.

Abstract

Traditional cytogenetic studies of ovarian stromal tumors are few, although trisomy 12 has been frequently documented with fluorescence in situ hybridization (FISH). In the current study, karyotypic analysis of four ovarian stromal tumors and a review of the literature suggest that numerical abnormalities of chromosomes 4 and 9 might also be important, possibly as secondary changes. To determine the frequency of 4, 9, and 12 aneuploidy in a larger group of ovarian tumors, FISH studies were performed on eight fibromas, three thecomas, one fibrothecoma, and five cellular fibromas. Trisomy 12 was identified in all five cellular fibromas as well as in two fibromas and the fibrothecoma. Gain of chromosome 9 was confined to the cellular fibromas. Loss of chromosomes 4 and/or 9 was prominent in the fibromas. These findings confirm the presence of trisomy 12 as a nonrandom chromosomal abnormality in ovarian stromal tumors. Moreover, these conventional and molecular cytogenetic data indicate that gain of chromosome 9 in addition to gain of chromosome 12 is prominent in cellular fibroma. In contrast, loss of chromosomes 4 and/or 9 are recurrent in fibroma. In summary, imbalances of chromosomes 4 and 9 appear to represent important secondary abnormalities in the thecoma-fibroma ovarian tumor group.

摘要

卵巢间质瘤的传统细胞遗传学研究较少,尽管荧光原位杂交(FISH)已频繁证实12号染色体三体。在本研究中,对4例卵巢间质瘤的核型分析及文献回顾表明,4号和9号染色体的数目异常可能也很重要,可能是继发改变。为确定更大一组卵巢肿瘤中4、9和12号染色体非整倍体的频率,对8例纤维瘤、3例卵泡膜瘤、1例纤维卵泡膜瘤和5例细胞性纤维瘤进行了FISH研究。在所有5例细胞性纤维瘤以及2例纤维瘤和1例纤维卵泡膜瘤中均检测到12号染色体三体。9号染色体增加仅限于细胞性纤维瘤。4号和/或9号染色体缺失在纤维瘤中较为突出。这些发现证实12号染色体三体是卵巢间质瘤中一种非随机的染色体异常。此外,这些传统和分子细胞遗传学数据表明,除了12号染色体增加外,9号染色体增加在细胞性纤维瘤中也很突出。相比之下,4号和/或9号染色体缺失在纤维瘤中较为常见。总之,4号和9号染色体的失衡似乎代表了卵泡膜瘤-纤维瘤卵巢肿瘤组中重要的继发异常。

相似文献

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本文引用的文献

8
Monosomy 22 in a fibrothecoma.
Cancer Genet Cytogenet. 1997 Dec;99(2):129-31. doi: 10.1016/s0165-4608(97)00210-0.

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