The Origin of Ovarian Carcinomas

间皮 上皮 生物 输卵管 移行上皮 病理 壶腹 肿瘤转化 恶性转化 解剖 癌症研究 癌变 内分泌学 癌症 医学 遗传学 大肠杆菌 腹膜 基因
作者
Nelly Auersperg
出处
期刊:International Journal of Gynecological Pathology [Lippincott Williams & Wilkins]
卷期号:30 (1): 12-21 被引量:127
标识
DOI:10.1097/pgp.0b013e3181f45f3e
摘要

It is currently a controversial issue whether epithelial ovarian cancers arise in the ovarian surface epithelium (OSE) or the fimbrial epithelium of the oviduct. The hypothesis presented here aims to reconcile these 2 views and provides a possible explanation for 2 questions arising: first, why tumors originating in the fimbriae and OSE, which are parts of different organs, express common features; second, why these epithelia are prone to neoplastic transformation whereas the remaining oviduct and the extraovarian mesothelium are not. We hypothesize that these questions relate to the common origin of the OSE and fimbriae in that region of the embryonic coelomic epithelium, which will eventually link the extraovarian mesothelium to the epithelium of the oviductal ampulla. OSE and fimbriae become separated during embryonic development but, like other transitional, interepithelial junctions in adults, this region might remain incompletely committed and thus prone to neoplastic progression. To define differentiation at the OSE-tubal junction, salpingo-oophorectomy specimens were stained immunohistochemically for mesenchymal differentiation markers of OSE and for epithelial markers and Pax8, characterizing oviductal fimbriae and ampullae. OSE and ampullae were distinctly different, but there was no sharp boundary between OSE and fimbriae. Rather, both mesenchymal and epithelial markers overlapped, and Pax8 and fimbrial epithelial markers diminished distally, near the OSE. The results support the hypothesis that the OSE and fimbriae are parts of a transitional epithelium of common origin rather than 2 independent sources of ovarian cancer, and suggest that their immature, incompletely determined phenotype contributes to their propensity to neoplastic transformation.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
yang发布了新的文献求助10
刚刚
叶若相怜完成签到,获得积分10
刚刚
失眠的云朵完成签到,获得积分10
刚刚
傲娇的迎曼完成签到,获得积分10
刚刚
flysteven92完成签到 ,获得积分10
刚刚
晨光完成签到,获得积分10
1秒前
Rainlistener完成签到,获得积分10
2秒前
廉洁发布了新的文献求助10
2秒前
赵念婉完成签到,获得积分10
3秒前
WJ1989完成签到,获得积分10
3秒前
研友_8Wz5MZ完成签到,获得积分10
3秒前
kangkang完成签到 ,获得积分10
4秒前
Alex完成签到 ,获得积分10
5秒前
ren完成签到,获得积分10
5秒前
5秒前
落日曜完成签到 ,获得积分10
5秒前
明理的南风完成签到,获得积分10
5秒前
Kay76完成签到,获得积分10
6秒前
Fang Xianxin完成签到,获得积分10
6秒前
Fly完成签到,获得积分10
6秒前
恒牙完成签到 ,获得积分10
6秒前
高山和鸟完成签到,获得积分10
7秒前
dou完成签到,获得积分10
7秒前
眼睛大天思完成签到,获得积分10
7秒前
望远山完成签到,获得积分10
8秒前
姗珊完成签到 ,获得积分10
8秒前
科研通AI2S应助鹿lu采纳,获得10
9秒前
fhl完成签到,获得积分20
9秒前
xsir完成签到 ,获得积分10
9秒前
zhan完成签到,获得积分10
9秒前
量子星尘发布了新的文献求助10
10秒前
Georges-09完成签到,获得积分10
10秒前
小圈圈梦魇完成签到,获得积分10
10秒前
10秒前
11秒前
zlg关注了科研通微信公众号
12秒前
FashionBoy应助yang采纳,获得10
12秒前
2026年我要发paper完成签到,获得积分10
13秒前
徐继军完成签到 ,获得积分10
13秒前
11发布了新的文献求助10
14秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Aerospace Standards Index - 2026 ASIN2026 3000
Polymorphism and polytypism in crystals 1000
Signals, Systems, and Signal Processing 610
Discrete-Time Signals and Systems 610
Research Methods for Business: A Skill Building Approach, 9th Edition 500
Social Work and Social Welfare: An Invitation(7th Edition) 410
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6051497
求助须知:如何正确求助?哪些是违规求助? 7861178
关于积分的说明 16268314
捐赠科研通 5196551
什么是DOI,文献DOI怎么找? 2780704
邀请新用户注册赠送积分活动 1763614
关于科研通互助平台的介绍 1645677