Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Int J Gynecol Cancer. 2012 Oct;22(8):1310-5. doi: 10.1097/IGC.0b013e31826b5dcc.
ARID1A is a recently identified tumor suppressor participating in chromatin remodeling. Somatic inactivating mutations of ARID1A and loss of its expression occur frequently in ovarian clear cell and endometrioid carcinomas and in uterine endometrioid carcinomas. Because endometriotic epithelium is thought to be the cell of origin of most ovarian clear cell and endometrioid carcinomas, we undertook an analysis of ARID1A expression of these tumors arising within an endometriotic cyst (endometrioma).
Our immunohistochemical study set consisted of 47 endometriotic cysts containing clear cell carcinoma in 24 cases, well-differentiated ovarian endometrioid carcinoma in 20 cases, and mixed clear cell and endometrioid carcinoma in 3 cases.
ARID1A loss was observed in 31 (66%) of 47 carcinomas; and therefore, these cases were informative for determining the temporal sequence of loss of ARID1A expression in tumor progression. In 16 of the 47 cases, ARID1A immunoreactivity was retained in both the endometriotic cyst and the carcinoma; and thus, these cases were not informative. All of the 31 informative cases showed loss of ARID1A immunoreactivity in the carcinoma and in the endometriotic cyst epithelium in direct continuity with the carcinoma but not in the cyst epithelium that was not adjacent to the tumor.
Loss of ARID1A function as shown by loss of expression, presumably due to mutations, is an early molecular event in the development of most ovarian clear cell and endometrioid carcinomas arising in endometriomas.
ARID1A 是一种新发现的肿瘤抑制因子,参与染色质重塑。ARID1A 的体细胞失活突变及其表达缺失在卵巢透明细胞癌和子宫内膜样癌以及子宫子宫内膜样癌中频繁发生。因为子宫内膜异位症上皮被认为是大多数卵巢透明细胞癌和子宫内膜样癌的起源细胞,我们对这些起源于子宫内膜异位囊肿(子宫内膜瘤)的肿瘤进行了 ARID1A 表达分析。
我们的免疫组织化学研究组包括 47 个含有透明细胞癌的子宫内膜异位囊肿,其中 24 例为分化良好的卵巢子宫内膜样癌,3 例为混合性透明细胞和子宫内膜样癌。
在 47 例癌中,观察到 ARID1A 缺失 31 例(66%);因此,这些病例有助于确定 ARID1A 表达缺失在肿瘤进展中的时间顺序。在 47 例中有 16 例,子宫内膜异位囊肿和癌中保留了 ARID1A 免疫反应性;因此,这些病例没有信息。所有 31 例有信息的病例均显示,癌和直接与癌连续的子宫内膜异位囊肿上皮中 ARID1A 免疫反应性缺失,但与肿瘤不相邻的囊肿上皮中 ARID1A 免疫反应性未缺失。
ARID1A 功能丧失(表现为表达缺失,可能由于突变)是大多数起源于子宫内膜瘤的卵巢透明细胞癌和子宫内膜样癌发展中的早期分子事件。