Department of Obstetrics and Gynecology, Shimane University School of Medicine, Izumo, Japan.
Mod Pathol. 2012 Feb;25(2):282-8. doi: 10.1038/modpathol.2011.161. Epub 2011 Nov 18.
Recently, the ARID1A gene has been identified as a novel tumor suppressor in ovarian clear cell carcinoma. The prognostic significance of the loss of ARID1A expression is not known. The current study was designed to evaluate whether ARID1A was a prognostic factor for progression, survival, and chemoresistance in ovarian clear cell carcinoma. A total of 60 patients, who were surgically treated for primary ovarian clear cell adenocarcinoma, were enrolled. Surgical specimens were examined for ARID1A protein expression by immunohistochemistry. The correlations between the loss of ARID1A expression and clinicopathological characteristics, prognosis, and chemosensitivity were investigated. Loss of ARID1A expression was identified in 9 (15.0%) of 60 ovarian clear cell carcinoma samples. Loss of ARID1A staining intensity (0+) was more frequently found in cells of clear cell carcinomas than in high-grade serous carcinomas (P<0.01). Loss of ARID1A expression was significantly correlated with advanced FIGO stage and high CA125 levels (P=0.02, 0.01). There were no significant correlations between loss of ARID1A expression and patient age, status of residual tumor, Ki-67 labeling index, or the status of endometriosis. Loss of ARID1A correlated with shorter progression-free survival of patients with clear cell carcinomas treated with platinum-based chemotherapy (P<0.01). Loss of ARID1A expression tended to correlate with shorter overall survival in patients with ovarian clear cell carcinomas treated with platinum-based chemotherapy. When data were stratified for the multivariate analysis, only the loss of ARID1A expression remained a significant (P=0.03) predictor of reduced progression-free survival. Of the 60 patients with ovarian clear cell carcinomas, 14 patients had measurable residual tumor after primary cytoreductive surgery. Tumors with loss of ARID1A expression were more likely to be chemoresistant than tumors with positive ARID1A expression (100.0 vs 40.0%, P=0.04). This study demonstrates that loss of ARID1A in ovarian clear cell carcinoma is a negative prognostic factor in patients treated with platinum-based chemotherapy. Measurement of ARID1A expression may be a method to predict resistance to platinum-based chemotherapy in patients with ovarian clear cell carcinoma.
最近,ARID1A 基因被鉴定为卵巢透明细胞癌中的一种新型肿瘤抑制因子。ARID1A 表达缺失的预后意义尚不清楚。本研究旨在评估 ARID1A 是否是卵巢透明细胞癌进展、生存和化疗耐药的预后因素。共纳入 60 例接受初次卵巢透明细胞腺癌手术治疗的患者。免疫组化法检测 ARID1A 蛋白表达。研究 ARID1A 缺失表达与临床病理特征、预后和化疗敏感性的关系。在 60 例卵巢透明细胞癌样本中,有 9 例(15.0%)存在 ARID1A 表达缺失。ARID1A 染色强度(0+)缺失在透明细胞癌中比高级别浆液性癌更为常见(P<0.01)。ARID1A 表达缺失与 FIGO 分期较晚和 CA125 水平较高显著相关(P=0.02,0.01)。ARID1A 表达缺失与患者年龄、肿瘤残留状态、Ki-67 标记指数或子宫内膜异位症状态均无显著相关性。在接受铂类化疗的透明细胞癌患者中,ARID1A 缺失与无进展生存期缩短相关(P<0.01)。在接受铂类化疗的卵巢透明细胞癌患者中,ARID1A 表达缺失与总生存期缩短相关。在多变量分析中分层数据时,只有 ARID1A 表达缺失仍然是无进展生存期缩短的显著预测因子(P=0.03)。在 60 例卵巢透明细胞癌患者中,有 14 例患者在初次细胞减灭性手术后有可测量的残留肿瘤。与 ARID1A 表达阳性的肿瘤相比,ARID1A 缺失的肿瘤更有可能对化疗耐药(100.0%比 40.0%,P=0.04)。本研究表明,卵巢透明细胞癌中 ARID1A 的缺失是接受铂类化疗的患者的预后不良因素。ARID1A 表达的测量可能是预测卵巢透明细胞癌患者对铂类化疗耐药的一种方法。