Cytoplasmic clusterin expression is associated with longer survival in patients with resected non-small cell lung cancer

被引:42
作者
Albert, Jeffrey M.
Gonzalez, Adriana
Massion, Pierre P.
Chen, Heidi
Olson, Sandra J.
Shyr, Yu
Diaz, Roberto
Lambright, Eric S.
Sandler, Alan
Carbone, David P.
Putnam, Joe B., Jr.
Johnson, David H.
Lu, Bo
机构
[1] Vanderbilt Univ, Dept Radiat Oncol, Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Pathol, Nashville, TN 37212 USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37212 USA
[4] Vanderbilt Univ, Sch Med, Dept Prevent Med, Nashville, TN 37212 USA
[5] Vanderbilt Univ, Sch Med, Dept Thorac Surg, Vanderbilt Ingram Canc Ctr, Nashville, TN 37212 USA
关键词
D O I
10.1158/1055-9965.EPI-07-0146
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Clusterin is a glycoprotein that has been implicated in many processes, including apoptosis, cell cycle regulation, and DNA repair. Previous studies have examined the prognostic value of clusterin expression in various malignancies. In the present study, we examined clusterin staining in tumors resected from patients with non-small cell lung cancer (NSCLC). Materials and Methods: Tumor specimens were obtained for 113 patients with completely resected NSCLC from paraffin-embedded tissue microarrays and stained with an antibody specific for clusterin. Staining patterns were observed and graded based on intensity and then correlated with clinical data. Results: Positive cytoplasmic clusterin staining was observed in 44 patients, and weak/negative staining was observed in 62 patients. Patients who had tumors that stained positive for cytoplasmic clusterin had significantly longer survival in multivariate analysis (hazard ratio 0.487, 95% confidence interval 0.27-0.89). A correlation was also observed for recurrence-free survival, which approached statistical significance (hazard ratio 0.345, 95% confidence interval 0.12-1.02). In univariate analysis, patients with clusterin-positive tumors had a 63% 3-year survival, whereas patients with clusterin-negative tumors had a 42% 3-year survival (P = 0.0108); clusterin-positive tumors also had significantly less recurrence W = 0.0231). Conclusions: Cytoplasmic clusterin staining is present in a substantial number of NSCLC tumors and may be a biomarker for longer survival in patients with surgically resected NSCLC.
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收藏
页码:1845 / 1851
页数:7
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