Cho Hye-Yon, Kim Kidong, Kim Yong-Beom, Kim Haeryoung, No Jae Hong
*Department of Obstetrics and Gynecology, Hallym University Dongtan Sacred Heart Hospital; †Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital; and ‡Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Int J Gynecol Cancer. 2017 Mar;27(3):412-419. doi: 10.1097/IGC.0000000000000908.
This study evaluated the expression patterns of nuclear factor erythroid 2-related factor 2 (Nrf2) and Kelch-like ECH-associated protein 1 (Keap1) and assessed their clinical value as prognostic indicators in ovarian cancer.
The expression patterns of Nrf2 and Keap1 were determined in 100 epithelial ovarian cancers by immunohistochemistry analyses. The associations of Nrf2 and Keap1 expression with clinicopathological characteristics of patients were evaluated. All patients received platinum-based chemotherapy. Chemoresistance was defined as recurrence within 6 months of first-line chemotherapy.
Cytoplasmic expression of Nrf2 and Keap1 was observed in 95% and 72%, respectively, of all 100 epithelial ovarian cancers examined. Low Keap1 expression (intensity < 1) was strongly associated with disease recurrence (P = 0.046) and death (P = 0.002). Chemoresistance was associated with high Nrf2 expression (intensity = 3) (P = 0.833; hazard ratio [HR], 1.202; 95% confidence interval [CI], 0.217-6.667) and low Keap1 expression (P = 0.862; HR, 0.899; 95% CI, 0.270-2.994). However, these associations were not statistically significant. Survival analysis indicated that high Keap1 expression (intensity ≥ 1) was strongly predictive of better overall survival (P = 0.049) and disease-free survival (P = 0.004). Cox regression analysis indicated that Keap1 expression was an independent prognostic factor for overall survival (P = 0.012; HR, 0.349; 95% CI, 0.153-0.797). Although patients with high Nrf2 expression displayed better overall survival and disease-free survival, the association was not statistically significant.
High cytoplasmic Keap1 expression, which might prevent nuclear translocation of Nrf2 in ovarian cancer cells, was associated with lower disease recurrence and death rate. Survival analysis suggested a probable role of Keap1 expression in predicting the prognosis of ovarian cancer.
本研究评估核因子红细胞2相关因子2(Nrf2)和 Kelch样ECH相关蛋白1(Keap1)的表达模式,并评估它们作为卵巢癌预后指标的临床价值。
通过免疫组织化学分析确定100例上皮性卵巢癌中Nrf2和Keap1的表达模式。评估Nrf2和Keap1表达与患者临床病理特征的相关性。所有患者均接受铂类化疗。化疗耐药定义为一线化疗后6个月内复发。
在所有100例接受检查的上皮性卵巢癌中,分别有95%和72%观察到Nrf2和Keap1的细胞质表达。低Keap1表达(强度<1)与疾病复发(P = 0.046)和死亡(P = 0.002)密切相关。化疗耐药与高Nrf2表达(强度= 3)(P = 0.833;风险比[HR],1.202;95%置信区间[CI],0.217 - 6.667)和低Keap1表达(P = 0.862;HR,0.899;95% CI,0.270 - 2.994)相关。然而,这些关联无统计学意义。生存分析表明,高Keap1表达(强度≥1)强烈预测总体生存期(P = 0.049)和无病生存期(P = 0.004)更好。Cox回归分析表明,Keap1表达是总体生存的独立预后因素(P = 0.012;HR,0.349;95% CI,0.153 - 0.797)。尽管高Nrf2表达的患者总体生存期和无病生存期较好,但该关联无统计学意义。
高细胞质Keap1表达可能阻止Nrf2在卵巢癌细胞中的核转位,与较低的疾病复发率和死亡率相关。生存分析提示Keap1表达在预测卵巢癌预后中可能起作用。