Osteopontin but not osteonectin messenger RNA expression is a prognostic marker in curatively resected non-small cell lung cancer

被引:66
作者
Schneider, S
Yochim, J
Brabender, J
Uchida, K
Danenberg, KD
Metzger, R
Schneider, PM
Salonga, D
Hölscher, AH
Danenberg, PV
机构
[1] Univ So Calif, Kenneth Norris Jr Comprehens Canc Ctr, Keck Sch Med, Los Angeles, CA 90033 USA
[2] Univ So Calif, Dept Mol Biol & Biochem, Keck Sch Med, Los Angeles, CA 90033 USA
[3] Univ Cologne, Dept Visceral & Vasc Surg, Cologne, Germany
[4] Response Genet Inc, Los Angeles, CA USA
关键词
D O I
10.1158/1078-0432.CCR-0565-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The purpose of this study was to better define the role of osteopontin (OPN) and osteonectin [also known as secreted protein acidic and rich in cysteine (SPARC)] in lung tumorigenesis by comparing the expressions of these genes in lung tumor tissue and matched normal tissue and by determining the prognostic significance of the gene expressions. Experimental Design: Quantitative real-time reverse transcription-PCR was used to analyze OPN and SPARC mRNA expression in normal lung tissue and matching tumor samples from 82 patients with non-small cell lung cancer. Gene expression data for each patient were matched to survival data. Results: The overall median mRNA expression level of OPN was about 20-fold higher in tumor tissues than in matching normal lung tissues (P < 0.001), whereas SPARC gene expression was not significantly different in both tissue types. Forty of 82 patients had high ( ≥ 4.1) intratumoral OPN expression, and 15 of 82 patients had high ( ≥ 15.5) SPARC expression. High OPN expression in the tumor tissue was associated with inferior survival (P = 0.014), whereas high SPARC expression showed a trend toward longer survival (P = 0.095). The impact of high OPN and low SPARC expression on patient survival was additive (P = 0.001). Conclusions: The large increase in OPN expression in tumors compared with normal tissue and its association with survival suggest a role for OPN in lung tumorigenesis.
引用
收藏
页码:1588 / 1596
页数:9
相关论文
共 53 条
[1]  
Agrawal D, 2002, J NATL CANCER I, V94, P513
[2]   Eta-1 (osteopontin): An early component of type-1 (cell-mediated) immunity [J].
Ashkar, S ;
Weber, GF ;
Panoutsakopoulou, V ;
Sanchirico, ME ;
Jansson, M ;
Zawaideh, S ;
Rittling, SR ;
Denhardt, DT ;
Glimcher, MJ ;
Cantor, H .
SCIENCE, 2000, 287 (5454) :860-864
[3]  
BAUTISTA DS, 1994, J BIOL CHEM, V269, P23280
[4]  
BEHREND EI, 1994, CANCER RES, V54, P832
[5]  
BELLAHCENE A, 1995, AM J PATHOL, V146, P95
[6]  
Bellahcene A, 1997, B CANCER, V84, P17
[7]   DIVERSITY OF FUNCTION IS INHERENT IN MATRICELLULAR PROTEINS - AN APPRAISAL OF THROMBOSPONDIN-1 [J].
BORNSTEIN, P .
JOURNAL OF CELL BIOLOGY, 1995, 130 (03) :503-506
[8]   Enhanced growth of tumors in SPARC null mice is associated with changes the ECM [J].
Brekken, RA ;
Puolakkainen, P ;
Graves, DC ;
Workman, G ;
Lubkin, SR ;
Sage, EH .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (04) :487-495
[9]   Osteopontin expression in lung cancer [J].
Chambers, AF ;
Wilson, SM ;
Kerkvliet, N ;
OMalley, FP ;
Harris, JF ;
Casson, AG .
LUNG CANCER, 1996, 15 (03) :311-323
[10]   Isolation of and effector for metastasis-inducing DNAs from a human metastatic carcinoma cell line [J].
Chen, HJ ;
Ke, YQ ;
Oates, AJ ;
Barraclough, R ;
Rudland, PS .
ONCOGENE, 1997, 14 (13) :1581-1588