Itamochi Hiroaki, Oumi Nao, Oishi Tetsuro, Shoji Tadahiro, Fujiwara Hiroyuki, Sugiyama Toru, Suzuki Mitsuaki, Kigawa Junzo, Harada Tasuku
Department of Obstetrics and Gynecology, Tottori University School of Medicine, 36-1 Nishicho, Yonago, Tottori, 683-8504, Japan.
Department of Obstetrics and Gynecology, Iwate Medical University, 19-1 Uchimaru, Morioka, Iwate, 020-8505, Japan.
Int J Clin Oncol. 2015 Oct;20(5):967-73. doi: 10.1007/s10147-015-0811-x. Epub 2015 Mar 6.
Recent studies have shown that somatic mutations in the AT-rich interactive domain 1A (SWI-like) gene (ARID1A) are the most common genetic changes in clear cell carcinoma of the ovary (CCC). A gene mutation of ARID1A was found in approximately half of CCC cases, and led to absence of the encoded protein and inactivation of the putative tumor suppressor. Here, we investigated whether ARID1A could be a prognostic biomarker for this disease.
We analyzed the protein expression of ARID1A in CCC from 112 patients by immunohistochemical staining, and evaluated the association of these molecular parameters with clinical outcome.
The loss of ARID1A expression was found in 39 % (44/112) of CCC, and was not associated with patient age, FIGO stage, and status of residual tumor. The 5-year survival rate for FIGO stage I or II patients with negative tumor expression of ARID1A was lower than those with positive tumor expression of ARID1A (74 % vs 91 %), but this difference was not observed in FIGO stage III or IV patients. Multivariable analysis revealed that ARID1A expression was an independent prognostic factor in FIGO stage I or II CCC patients.
ARID1A may be a biomarker that is predictive of the outcome of FIGO stage I and II CCC.
最近的研究表明,富含AT的相互作用结构域1A(SWI样)基因(ARID1A)的体细胞突变是卵巢透明细胞癌(CCC)中最常见的基因改变。在大约一半的CCC病例中发现了ARID1A基因突变,这导致编码蛋白缺失以及假定的肿瘤抑制因子失活。在此,我们研究了ARID1A是否可能是这种疾病的预后生物标志物。
我们通过免疫组织化学染色分析了112例患者的CCC中ARID1A的蛋白表达,并评估了这些分子参数与临床结局的相关性。
在39%(44/112)的CCC中发现ARID1A表达缺失,且与患者年龄、国际妇产科联盟(FIGO)分期及残留肿瘤状态无关。FIGO I期或II期肿瘤ARID1A表达阴性的患者5年生存率低于ARID1A表达阳性的患者(74%对91%),但在FIGO III期或IV期患者中未观察到这种差异。多变量分析显示,ARID1A表达是FIGO I期或II期CCC患者的独立预后因素。
ARID1A可能是预测FIGO I期和II期CCC结局的生物标志物。