Tsakonas Georgios, Martín-Bernabé Alfonso, Rounis Konstantinos, Moreno-Ruiz Pablo, Botling Johan, De Petris Luigi, Ylipää Antti, Mezheyeuski Artur, Micke Patrick, Östman Arne, Ekman Simon
Thoracic Oncology Center, Theme Cancer, Karolinska University Hospital, Solna, 17164 Stockholm, Sweden.
Department of Oncology-Pathology, Karolinska Institutet, 17164 Stockholm, Sweden.
Cancers (Basel). 2021 Jun 24;13(13):3151. doi: 10.3390/cancers13133151.
Nuclear factor erythroid 2-related factor 2 (NRF2) protein expression promotes cancer progression in non-small cell lung cancer (NSCLC). However, its role in the clinical setting has not been established. We retrospectively analyzed data from 304 patients with surgically removed NSCLC. Multiplex antibody staining of NRF2 and thioredoxin reductase 1 (TrxR1) was conducted and scored in cytokeratin-positive (CK+) cells within the whole-tissue core as well as the tumor and stromal compartments of each tissue microarray (TMA) core. A high density of NRF2+/CK+ cells in the whole-tissue core compartment was correlated with a higher risk of central nervous system (CNS) relapse OR = 7.36 (95% CI: 1.64-33.06). The multivariate analysis showed an OR = 8.00 (95% CI: 1.70-37.60) for CNS relapse in NRF2+/CK+ high-density cases. The density of TrxR1+/CK+ cells failed to show any statistically significant risk of relapse. The OS analyses for NRF2+/CK+ and TrxR1+/CK+ cell density failed to show any statistical significance. This is the first study to report a correlation between NRF2+/CK+ cell density and the risk of CNS relapse in early-stage NSCLC. The results of our study may impact the follow-up strategy for early-stage NSCLC patients and eventually improve their prognosis.
核因子红细胞2相关因子2(NRF2)蛋白表达促进非小细胞肺癌(NSCLC)的癌症进展。然而,其在临床环境中的作用尚未明确。我们回顾性分析了304例接受手术切除的NSCLC患者的数据。对NRF2和硫氧还蛋白还原酶1(TrxR1)进行多重抗体染色,并在全组织核心以及每个组织微阵列(TMA)核心的肿瘤和基质区域的细胞角蛋白阳性(CK+)细胞中进行评分。全组织核心区域中高密度的NRF2+/CK+细胞与中枢神经系统(CNS)复发风险较高相关,OR = 7.36(95%CI:1.64 - 33.06)。多变量分析显示,NRF2+/CK+高密度病例发生CNS复发的OR = 8.00(95%CI:1.70 - 37.60)。TrxR1+/CK+细胞密度未显示出任何具有统计学意义的复发风险。对NRF2+/CK+和TrxR1+/CK+细胞密度的总生存期分析未显示出任何统计学意义。这是第一项报道NRF2+/CK+细胞密度与早期NSCLC中枢神经系统复发风险之间相关性的研究。我们的研究结果可能会影响早期NSCLC患者的随访策略,并最终改善他们的预后。