The Combination Of Weak Expression Of PRDX4 And Very High MIB-1 Labelling Index Independently Predicts Shorter Disease-free Survival In Stage I Lung Adenocarcinoma

被引:16
|
作者
Shioya, Akihiro [1 ]
Guo, Xin [1 ]
Motono, Nozomu [2 ]
Mizuguchi, Seiya [3 ]
Kurose, Nozomu [1 ,3 ]
Nakada, Satoko [1 ,3 ]
Aikawa, Akane [1 ,3 ]
Ikeda, Yoshitaka [4 ]
Uramoto, Hidetaka [2 ]
Yamada, Sohsuke [1 ,3 ]
机构
[1] Kanazawa Med Univ, Dept Pathol & Lab Med, 1-1 Daigaku, Uchinada, Ishikawa 9200293, Japan
[2] Kanazawa Med Univ, Dept Thorac Surg, Uchinada, Ishikawa, Japan
[3] Kanazawa Med Univ, Dept Pathol, Uchinada, Ishikawa, Japan
[4] Saga Univ, Dept Biomol Sci, Div Mol Cell Biol, Fac Med, Saga, Japan
来源
INTERNATIONAL JOURNAL OF MEDICAL SCIENCES | 2018年 / 15卷 / 10期
基金
中国国家自然科学基金;
关键词
lung adenocarcirtoma (LUAD); stage I; PRDX4; MIB-1; recurrence; PEROXIREDOXIN; 4; PROTECTS; IMMUNOHISTOCHEMICAL EXPRESSION; MUCIN ANTIGENS; OVEREXPRESSION; CLASSIFICATION; IDENTIFICATION; ASSOCIATION; PROGNOSIS; CARCINOMA; SURGERY;
D O I
10.7150/ijms.25734
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Oxidative stress plays pivotal roles in the progression of lung adenocarcinoma (LUAD) through cell signaling related closely to cancer growth. We previously reported that peroxiredoxin 4 (PRDX4), a secretory-type antioxidant enzyme, can protect against the development of various diseases, including potential malignancies. Since many patients with early-stage LUAD develop recurrence, even after curative complete resection, we investigated the association of the PRDX4 expression with the clinicopathological features and recurrence/prognosis using post-surgical samples of stage I-LUAD. Methods: The expression of PRDX4 and MIB-1, a widely accepted Ki67 protein, was immunohistochemically analysed in 206 paraffin-embedded tumour specimens of patients with stage I-LUAD. The PRDX4 expression was considered to be weak when less than 25% of the adenocarcinoma cells showed positive staining. Results: A weak PRDX4+ expression demonstrated a significantly close relationship with pathologically poor differentiation, highly invasive characteristics and recurrence. The decrease in PRDX4-positivity potentially induced cell growth in LUAD, which was correlated significantly with a very high MIB-1 labelling index (>= 17.3%). Univariate/multivariate analyses revealed that the subjects with both weak PRDX4+ expression and a very high MIB-1 index had significantly worse disease-free survival rates than other subjects. Conclusions: The combination of weak PRDX4 expression and a very high MIB-1 index can predict high proliferating activity and recurrence with a potential poor prognosis, especially in post-operative stage I-LUAD patients.
引用
收藏
页码:1025 / 1034
页数:10
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