Mutations in Keap1 Are a Potential Prognostic Factor in Resected Non-small Cell Lung Cancer

被引:70
作者
Takahashi, Tsuyoshi
Sonobe, Makoto [1 ]
Menju, Toshi
Nakayama, El
Mino, Nobuya
Iwakiri, Shotaro
Nagai, Shinjiro
Sato, Kiyoshi
Miyahara, Ryo
Okubo, Kenichi
Hirata, Toshiki
Date, Hiroshi
Wada, Hiromi [2 ]
机构
[1] Kyoto Univ, Fac Med, Dept Thorac Surg, Sakyo Ku, Kyoto 6068507, Japan
[2] Osaka Wada Clin, Osaka, Japan
关键词
Kelch-like ECH-associated protein 1 (Keap1); mutation; prognosis; disease-free survival rate; non-small cell lung cancer (NSCLC); CUL3-BASED E3 LIGASE; OXIDATIVE STRESS; CYSTEINE RESIDUES; NRF2; PROTEIN; UBIQUITINATION; RESISTANCE; GENES; CHEMOTHERAPY; ACTIVATION;
D O I
10.1002/jso.21520
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Mutations in Kelch-like ECH-associated protein 1 (Keap 1) have been reported to protect tumor cells from chemotherapeutic agents. However, their prognostic significance in nonsmall cell lung cancer (NSCLC) is still unclear. In this study, we examined the effect of Keep! gene mutations on survival and disease-free interval using resected primary NSCLC tissue. Methods: We retrospectively analyzed the tumors from 79 patients with completely resected pathological Stage I-II NSCLC for the presence of Keap1 gene mutations and examined the prognosis of the patients. = Results: Keap1 gene mutations were detected in four patients (5.1%). The postoperative 5-year survival rate for patients with Keap1 mutations was significantly lower than those without a mutation (25% vs. 76%, P = 0.038). The postoperative 5-year disease-free survival rate for patients with a mutant Keap1 tumor was slightly lower than for patients with Keap1 wild-type tumors (25% vs. 66%, P = 0.057). Conclusions: Keap1 gene mutations are likely to be associated with a worse prognosis and lower postoperative disease-free survival rates in pathological Stage I-II NSCLC. J. Surg. Oncol. 2010:101:500-506. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:500 / 506
页数:7
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