Expression Patterns of Nrf2 and Keap1 in Ovarian Cancer Cells and their Prognostic Role in Disease Recurrence and Patient Survival.

Hye-Yon Cho, Kidong Kim, Yong-Beom Kim, Haeryoung Kim, Jae Hong No
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Abstract

Objective: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

Nrf2和Keap1在卵巢癌细胞中的表达模式及其在疾病复发和患者生存中的预后作用
目的:研究核因子红细胞2相关因子2 (Nrf2)和kelch样ech相关蛋白1 (Keap1)在卵巢癌中的表达规律,并评价其作为预后指标的临床价值。方法:采用免疫组化方法检测100例上皮性卵巢癌组织中Nrf2和Keap1的表达谱。评估Nrf2和Keap1表达与患者临床病理特征的关系。所有患者均接受铂类化疗。化疗耐药定义为一线化疗6个月内复发。结果:在100例上皮性卵巢癌中,Nrf2和Keap1的细胞质表达率分别为95%和72%。Keap1低表达(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Nrf2高表达相关(强度= 3)(P = 0.833;风险比[HR], 1.202;95%可信区间[CI], 0.217-6.667), Keap1低表达(P = 0.862;人力资源,0.899;95% ci, 0.270-2.994)。然而,这些关联在统计学上并不显著。生存分析显示,Keap1高表达(强度≥1)可显著预测总生存期(P = 0.049)和无病生存期(P = 0.004)。Cox回归分析显示,Keap1表达是影响总生存的独立预后因素(P = 0.012;人力资源,0.349;95% ci, 0.153-0.797)。虽然Nrf2高表达的患者表现出更好的总生存期和无病生存期,但这种相关性没有统计学意义。结论:Keap1在卵巢癌细胞质中的高表达与较低的疾病复发率和死亡率相关,并可能抑制Nrf2的核易位。生存分析提示Keap1表达可能对卵巢癌的预后有预测作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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