Heat shock protein 72 expression in osteosarcomas correlates with good response to neoadjuvant chemotherapy

被引:60
作者
Trieb, K
Lechleitner, T
Lang, S
Windhager, R
Kotz, R
Dirnhofer, S
机构
[1] Univ Innsbruck, Dept Pathol, A-6020 Innsbruck, Austria
[2] Univ Vienna, Dept Orthopaed, A-1010 Vienna, Austria
[3] Univ Vienna, Dept Pathol, A-1010 Vienna, Austria
关键词
osteosarcoma; heat shock protein; predictive marker; chemotherapy;
D O I
10.1016/S0046-8177(98)90412-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Although the therapeutic outcome of osteosarcoma patients has improved dramatically within the last 20 years because of combined neoadjuvant chemotherapy and surgery, the problem of drug resistance remains. Thus far, markers that can predict the response to chemotherapy at the time of biopsy are not available. Heat shock proteins (hsp) 60, 72, and 73 have been shown to pig a role in tumor immunity, and our study investigated their expression in human osteosarcomas and nonmalignant bone tumors before neoadjuvant chemotherapy. Immunohistochemical evaluations of hsp expression was performed on paraffin-embedded sections of 45 patients (17 female, 28 male, aged 6.5 to 62 years; mean, 19.4 years) with high-grade osteosarcoma at the time of biopsy, before preoperative chemotherapy. These results were correlated to histological response to chemotherapy, tumor size, age, alkaline phosphatase serum levels, and duration of symptoms. Thirty-four patients (15 male, 19 female, mean age 27 years) with osteoblastoma, osteoid-osteoma, or fibrous dysplasia served as nonmalignant controls. Hsp60 was uniformly found in the cytoplasm of both benign and malignant bone tumors. Nuclear hsp73 expression quatitatively increased in osteosarcoma cells. Hsp72 was significantly overexpressed in osteosarcomas (17 of 45, 38%) compared with nonmalignant bone tumors (1 of 34, 2.9%; P < .001). Hsp72-positive osteosarcomas responded better to neoadjuvant chemotherapy than hsp72-negative cases (P < .001), coexpress hsp60, and correlate with higher tumor size (P < .005) and location in the distal femur. No differences were observed relative to ge, gender, duration of symptoms, alkaline phosphatase levels, or hsp73 expression between hsp72-positive and hsp72-negative turners. Hsp72 expression seemed to be a predictive immunohistochemical marker for osteosarcoma, because it is the first marker to prospectively correlate to response to neoadjuvant chemotherapy. It therefore, may be of importance in preoperative therapy regimens for nonresponding high-risk patients. Copyright (C) 1998 by W.B. Saunders Company.
引用
收藏
页码:1050 / 1055
页数:6
相关论文
共 45 条
[1]  
BACCI G, 1987, CLIN ORTHOP RELAT R, P268
[2]  
BACCI G, 1991, CLIN ORTHOP RELAT R, P87
[3]   EXPRESSION OF P-GLYCOPROTEIN IN HIGH-GRADE OSTEOSARCOMAS IN RELATION TO CLINICAL OUTCOME [J].
BALDINI, N ;
SCOTLANDI, K ;
BARBANTIBRODANO, G ;
MANARA, MC ;
MAURICI, D ;
BACCI, G ;
BERTONI, F ;
PICCI, P ;
SOTTILI, S ;
CAMPANACCI, M ;
SERRA, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 333 (21) :1380-1385
[4]   WET AUTOCLAVE PRETREATMENT FOR ANTIGEN RETRIEVAL IN DIAGNOSTIC IMMUNOHISTOCHEMISTRY [J].
BANKFALVI, A ;
NAVABI, H ;
BIER, B ;
BOCKER, W ;
JASANI, B ;
SCHMID, KW .
JOURNAL OF PATHOLOGY, 1994, 174 (03) :223-228
[5]  
BENTZEN SM, 1988, CANCER-AM CANCER SOC, V62, P194, DOI 10.1002/1097-0142(19880701)62:1<194::AID-CNCR2820620129>3.0.CO
[6]  
2-8
[7]   Tumor size and prognosis in aggressively treated osteosarcoma [J].
Bieling, P ;
Rehan, N ;
Winkler, P ;
Helmke, K ;
Maas, R ;
Fuchs, N ;
Bielack, S ;
Heise, U ;
Jurgens, H ;
Treuner, J ;
Romanowski, R ;
Exner, U ;
Kotz, R ;
Winkler, K .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (03) :848-858
[8]   MECHANISM OF MULTIDRUG RESISTANCE [J].
BRADLEY, G ;
JURANKA, PF ;
LING, V .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 948 (01) :87-128
[9]  
CAMPANACCI M, 1981, CANCER, V48, P1569, DOI 10.1002/1097-0142(19811001)48:7<1569::AID-CNCR2820480717>3.0.CO
[10]  
2-X