Department of Human Genetics, McGill University, Montreal, Canada.
PLoS One. 2011;6(12):e28250. doi: 10.1371/journal.pone.0028250. Epub 2011 Dec 6.
Ovarian carcinomas exhibit extensive heterogeneity, and their etiology remains unknown. Histological and genetic evidence has led to the proposal that low grade ovarian serous carcinomas (LGOSC) have a different etiology than high grade carcinomas (HGOSC), arising from serous tumours of low malignant potential (LMP). Common regions of chromosome (chr) 3 loss have been observed in all types of serous ovarian tumours, including benign, suggesting that these regions contain genes important in the development of all ovarian serous carcinomas. A high-density genome-wide genotyping bead array technology, which assayed >600,000 markers, was applied to a panel of serous benign and LMP tumours and a small set of LGOSC, to characterize somatic events associated with the most indolent forms of ovarian disease. The genomic patterns inferred were related to TP53, KRAS and BRAF mutations. An increasing frequency of genomic anomalies was observed with pathology of disease: 3/22 (13.6%) benign cases, 40/53 (75.5%) LMP cases and 10/11 (90.9%) LGOSC cases. Low frequencies of chr3 anomalies occurred in all tumour types. Runs of homozygosity were most commonly observed on chr3, with the 3p12-p11 candidate tumour suppressor region the most frequently homozygous region in the genome. An LMP harboured a homozygous deletion on chr6 which created a GOPC-ROS1 fusion gene, previously reported as oncogenic in other cancer types. Somatic TP53, KRAS and BRAF mutations were not observed in benign tumours. KRAS-mutation positive LMP cases displayed significantly more chromosomal aberrations than BRAF-mutation positive or KRAS and BRAF mutation negative cases. Gain of 12p, which harbours the KRAS gene, was particularly evident. A pathology review reclassified all TP53-mutation positive LGOSC cases, some of which acquired a HGOSC status. Taken together, our results support the view that LGOSC could arise from serous benign and LMP tumours, but does not exclude the possibility that HGOSC may derive from LMP tumours.
卵巢癌表现出广泛的异质性,其病因仍不清楚。组织学和遗传学证据表明,低级别卵巢浆液性癌 (LGOSC) 的病因与高级别癌 (HGOSC) 不同,后者源于低恶性潜能的浆液性肿瘤 (LMP)。在所有类型的浆液性卵巢肿瘤中,包括良性肿瘤,都观察到染色体 (chr) 3 缺失的常见区域,这表明这些区域包含在所有卵巢浆液性癌发展中重要的基因。应用一种高密度全基因组基因分型珠阵列技术 (检测了超过 60 万个标记物),对一组浆液性良性和 LMP 肿瘤以及一小部分 LGOSC 进行了检测,以表征与卵巢疾病最惰性形式相关的体细胞事件。推断出的基因组模式与 TP53、KRAS 和 BRAF 突变有关。随着疾病病理学的发展,观察到基因组异常的频率逐渐增加:3/22(13.6%)良性病例、40/53(75.5%)LMP 病例和 10/11(90.9%)LGOSC 病例。所有肿瘤类型的 chr3 异常发生率都较低。杂合性缺失最常见于 chr3,3p12-p11 候选肿瘤抑制区是基因组中最常纯合的区域。一个 LMP 在 chr6 上发生了纯合缺失,产生了 GOPC-ROS1 融合基因,以前在其他癌症类型中被报道为致癌基因。良性肿瘤中未观察到体细胞 TP53、KRAS 和 BRAF 突变。KRAS 突变阳性的 LMP 病例与 BRAF 突变阳性或 KRAS 和 BRAF 突变阴性病例相比,显示出明显更多的染色体异常。12p 的增益尤其明显,该区域包含 KRAS 基因。一项病理学复查重新分类了所有 TP53 突变阳性的 LGOSC 病例,其中一些获得了 HGOSC 状态。总的来说,我们的结果支持 LGOSC 可能源自浆液性良性和 LMP 肿瘤的观点,但不能排除 HGOSC 可能源自 LMP 肿瘤的可能性。