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首页> 外文期刊>Gynecological endocrinology: the official journal of the International Society of Gynecological Endocrinology >Novel insights on the malignant transformation of endometriosis into ovarian carcinoma
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Novel insights on the malignant transformation of endometriosis into ovarian carcinoma

机译:关于子宫内膜异位恶性转化为卵巢癌的新见解

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摘要

The malignant transformation of endometriosis is an uncommon event, which happens in 0.7-2.5% of the cases, and, when occurs, it usually involves the ovary. A 2 to 3-fold higher risk of ovarian endometrioid and clear cell carcinoma has been reported in women with endometriosis. Pathological studies have detected a morphological continuum of sequential steps from normal endometriotic cyst epithelium to atypical endometriosis and finally to invasive carcinoma. Ovarian endometrioid carcinoma harbors mutations of CTNNB1 in 16-53.3%, of PTEN in 14-20% and of ARID1A in 30-55% of the cases. Ovarian clear cell carcinoma harbors mutations of PIK3CA in 20-40% and of ARID1 in 15-75% of the cases. Whereas estrogen receptors and progesterone receptors are quite always absent, HNF-1b is often over-expressed in this histotype. Atypical endometriosis and endometriosis-related ovarian neoplasms share molecular alterations, such as PTEN mutations, ARID1A mutations and up-regulation of HNF-1b. Moreover, ARID1A mutations have been noted in clear cell tumors and contiguous atypical endometriosis, but not in distant endometriotic lesions. The loss of BAF250a protein expression is suggestive for the presence of ARID1A mutations, and represents an useful marker of malignant transformation of endometriosis.
机译:子宫内膜异位的恶性转化是罕见的事件,发生在0.7-2.5%的病例中,并且一旦发生,通常累及卵巢。据报道,患有子宫内膜异位症的女性患卵巢子宫内膜样癌和透明细胞癌的风险高2至3倍。病理学研究已发现从正常子宫内膜异位囊肿上皮到非典型子宫内膜异位,最后到浸润性癌的连续步骤的形态学连续体。卵巢子宫内膜样癌的CTNNB1突变占16-53.3%,PTEN突变占14-20%,而ARID1A突变占30-55%。卵巢透明细胞癌的PIK3CA突变占20-40%,而ARID1突变占15-75%。尽管雌激素受体和孕激素受体经常不存在,但在这种组织型中HNF-1b通常过表达。非典型子宫内膜异位症和与子宫内膜异位症相关的卵巢肿瘤具有分子改变,如PTEN突变,ARID1A突变和HNF-1b上调。此外,已经在透明细胞肿瘤和连续的非典型子宫内膜异位症中发现了ARID1A突变,但在远处的子宫内膜异位病灶中却没有发现。 BAF250a蛋白表达的丧失暗示ARID1A突变的存在,并且代表子宫内膜异位症恶性转化的有用标志。

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