The serum activity of thioredoxin reductases 1 (TrxR1) is correlated with the poor prognosis in EGFR wild-type and ALK negative non-small cell lung cancer

被引:13
作者
Chen, Gong [1 ]
Chen, Qiong [1 ]
Zeng, Fanxu [1 ]
Zeng, Liang [1 ]
Yang, Haiyan [1 ]
Xiong, Yi [1 ]
Zhou, Chunhua [1 ]
Liu, Li [1 ]
Jiang, Wenjuan [1 ]
Yang, Nong [1 ]
Zhang, Yongchang [1 ]
机构
[1] Hunan Canc Hosp, Affiliated Canc Hosp, Xiangya Sch Med, Dept Med Oncol,Lung Canc & Gastrointestinal Unit, Changsha 410013, Hunan, Peoples R China
基金
中国国家自然科学基金; 湖南省自然科学基金;
关键词
thioredoxin reductases 1; bio-marker; EGFR wild type and ALK negative non-small-cell lung cancer; CEA; prognosis; DNA-REPAIR; KAPPA-B; EXPRESSION; RESISTANCE; ACTIVATION; MECHANISMS; INHIBITOR; APOPTOSIS; BIOMARKER;
D O I
10.18632/oncotarget.23252
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The thioredxin reductases 1 (TrxR1) is one of the major antioxidant and redox regulators in mammalian cells. Studies have shown that TrxR1 is over expressed in many malignancy diseases. However, few studies have evaluated the role of TrxR1 in non-small cell lung cancer (NSCLC). Methods: Serum levels of TrxR1 and CEA in 142 patients with EGFR wild type and ALK negative advanced NSCLC was measured by ELISA assay before first line standard doublet chemotherapy from June 2013 to February 2016 in Hunan Cancer Hospital. Clinical characteristics and Survival data were collected and analyzed according to serum TrxR1 levels. Results: No significant differences were founded from clinic pathological variables. With the cut-off value of 12U/mL, the lower serum TrxR1 activity patients had long progression-free survival (PFS) and overall survival (OS) compared with higher patients (PFS: 5.3m vs. 3.6m p=0.044, OS: 14.5m vs. 11m p<0.001). In subgroup, lower serum TrxR1 activity patients had long OS both in adenocarcinoma (ADC) (17m vs. 8m, p=0.003) and squamous cell carcinoma (SCC) (13m vs. 11m, p=0.035). While combining with TrxR1 activity and serum CEA concentrations, we founded that patients with lower serum TrxR1 activity and serum CEA concentrations had long OS compared with higher group patients (20m vs. 7m, p<0.001). Conclusions: Serum TrxR1 activity was not affected by clinic pathological variables. Measurement of serum TrxR1 activity might be an independent prognostic factor for EGFR wild type and ALK negative advanced NSCLC patients. Combination of serum TrxR1 activity and serum CEA concentrations need to be further profiled from bench to beside.
引用
收藏
页码:115270 / 115279
页数:10
相关论文
共 28 条
  • [1] Biaglow JE, 2005, CANCER BIOL THER, V4, P6
  • [2] Small molecule inhibitors of mammalian thioredoxin reductase
    Cai, Wenqing
    Zhang, Liangwei
    Song, Yanlin
    Wang, Baolin
    Zhang, Baoxin
    Cui, Xuemei
    Hu, Guanming
    Liu, Yaping
    Wu, Jincai
    Fang, Jianguo
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2012, 52 (02) : 257 - 265
  • [3] TrxR1 as a Potent Regulator of the Nrf2-Keap1 Response System
    Cebula, Marcus
    Schmidt, Edward E.
    Arner, Elias S. J.
    [J]. ANTIOXIDANTS & REDOX SIGNALING, 2015, 23 (10) : 823 - 853
  • [4] Biomarker Analyses and Final Overall Survival Results From a Phase III, Randomized, Open-Label, First-Line Study of Gefitinib Versus Carboplatin/Paclitaxel in Clinically Selected Patients With Advanced Non-Small-Cell Lung Cancer in Asia (IPASS)
    Fukuoka, Masahiro
    Wu, Yi-Long
    Thongprasert, Sumitra
    Sunpaweravong, Patrapim
    Leong, Swan-Swan
    Sriuranpong, Virote
    Chao, Tsu-Yi
    Nakagawa, Kazuhiko
    Chu, Da-Tong
    Saijo, Nagahiro
    Duffield, Emma L.
    Rukazenkov, Yuri
    Speake, Georgina
    Jiang, Haiyi
    Armour, Alison A.
    To, Ka-Fai
    Yang, James Chih-Hsin
    Mok, Tony S. K.
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (21) : 2866 - 2874
  • [5] Modulation of oxidative stress as an anticancer strategy
    Gorrini, Chiara
    Harris, Isaac S.
    Mak, Tak W.
    [J]. NATURE REVIEWS DRUG DISCOVERY, 2013, 12 (12) : 931 - 947
  • [6] Cancer drug resistance: an evolving paradigm
    Holohan, Caitriona
    Van Schaeybroeck, Sandra
    Longley, Daniel B.
    Johnston, Patrick G.
    [J]. NATURE REVIEWS CANCER, 2013, 13 (10) : 714 - 726
  • [7] Jemal A, 2009, CA-CANCER J CLIN, V59, P225, DOI [10.3322/caac.20006, 10.3322/caac.21254, 10.3322/caac.21332, 10.3322/caac.21551, 10.3322/caac.20073, 10.3322/caac.21387, 10.3322/caac.21654, 10.3322/caac.21601]
  • [8] Kakolyris S, 2001, CLIN CANCER RES, V7, P3087
  • [9] The mechanism of apoptosis induced by a novel thioredoxin reductase inhibitor in A549 cells:: Possible involvement of nuclear factor-κB-dependent pathway
    Lan, Linxiang
    Zhao, Fang
    Wang, Yan
    Zeng, Huihui
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 555 (2-3) : 83 - 92
  • [10] CISPLATIN SENSITIVITY RESISTANCE IN UV REPAIR-DEFICIENT CHINESE-HAMSTER OVARY CELLS OF COMPLEMENTATION GROUP-1 AND GROUP-3
    LEE, KB
    PARKER, RJ
    BOHR, V
    CORNELISON, T
    REED, E
    [J]. CARCINOGENESIS, 1993, 14 (10) : 2177 - 2180