Oct4 Expression in Immature Teratoma of the Ovary

神经上皮细胞 生物 畸胎瘤 病理 未成熟畸胎瘤 免疫组织化学 卵巢畸胎瘤 SOX2 卵巢 同源盒蛋白纳米 胚胎干细胞 干细胞 神经干细胞 生殖细胞肿瘤 医学 免疫学 内分泌学 细胞生物学 诱导多能干细胞 遗传学 基因 化疗
作者
Kaoru Abiko,Masaki Mandai,Junzo Hamanishi,Noriomi Matsumura,Tsukasa Baba,Akiko Horiuchi,Yoshiki Mikami,Shinya Yoshioka,Tomoko Wakasa,Tanri Shiozawa,Ikuo Konishi
出处
期刊:The American Journal of Surgical Pathology [Lippincott Williams & Wilkins]
卷期号:34 (12): 1842-1848 被引量:49
标识
DOI:10.1097/pas.0b013e3181fcd707
摘要

Immature teratoma of the ovary is an uncommon tumor comprising 1% of ovarian malignancies. The amount of immature neuroepithelium in the teratoma is an important prognostic factor. Although the current grading system based on this criterion is widely accepted, the biological significance of immature neuroepithelium is poorly understood. In this study, we used immunohistochemistry to evaluate the expression of Oct4 (also known as Oct3 or POU5F1), a transcription factor expressed in primordial germ cells and embryonic stem cells, along with that of PAX6, a transcription factor contributing to neurogenesis, and CD56, a known marker for tumors of neural origin, in 18 cases of pure immature teratoma of the ovary. Oct4 was expressed in the immature neuroepithelium of all 7 grade-3 cases and 2 grade-2 cases. It was not expressed in 4 grade-2 cases and all 5 grade-1 cases. These tumor cells lacked CD30 or α-fetoprotein expression, which supported the diagnosis of pure immature teratoma. PAX6 was expressed in the immature neuroepithelium of all immature teratomas, but not in Oct4-positive cells. CD56 was expressed in neural components of various maturities including PAX6-positive immature neuroepithelium, but not in Oct4-positive cells. These data suggest that the expression of these markers probably reflects the differentiation status of neural tissue in immature teratomas. The finding that Oct4 expression was exclusively detected in immature neuroepithelium of high-grade immature teratomas indicates that Oct4 might serve as a promising biomarker for the diagnosis of highly malignant cases of immature teratoma.
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