Immunohistochemical analysis of inducible nitric oxide synthase (iNOS) and heat shock proteins (HSPs) in ameloblastomas

被引:28
作者
Kumamoto, H [1 ]
Suzuki, T [1 ]
Ooya, K [1 ]
机构
[1] Tohoku Univ, Grad Sch Dent, Dept Oral Med & Bioregulat, Div Oral Pathol,Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
ameloblastoma; heat shock protein (HSP); inducible nitric oxide synthase (iNOS);
D O I
10.1034/j.1600-0714.2002.00014.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background: To clarify the possible role of nitric oxide (NO) and stress proteins in ocogenesis and cytodifferentiation of odontogenic epithelium. Inducible NO synthase (iNOS) and heat shock proteins (HSPs) were analyzed in ameloblastomas as well as in tooth germs. Methods: Specimens of seven tooth germs, 36 benign ameloblastomas and five malignant ameloblastomas were examined by immunohistochemistry using antibodies against iNOS and 27-, 60- and 70-kDa HSPs (HSP27, HSP60 and HSP70). Results: Immunoreactivity for iNOS was detected in normal and neoplastic odontogenic epithelial cells and was higher in malignant ameloblastomas than in tooth germs and benign ameloblastomas. HSP27 was expressed constitutively in all odontogenic epithelial cells in tooth germs and benign and malignant ameloblastomas. Expression of HSP60 and HSP70 was detected in normal and neoplastic odontogenic epithelial cells and was prominent in cells neighboring the basement membrane. HSP60 reactivity showed no apparent difference between normal and neoplastic odontogenic epithelium, whereas HSP70 expression was slightly higher in benign and malignant ameloblastomas than in tooth germs. Conclusions: Activation of iNOS might be associated with malignant potential of epithelial odontogenic tumors. Elevated expression of HSP70 is considered to be involved in neoplastic transformation of odontogenic epithelial cells.
引用
收藏
页码:605 / 611
页数:7
相关论文
共 44 条
[1]   Relationship between p53 mutations and inducible nitric oxide synthase expression in human colorectal cancer [J].
Ambs, S ;
Bennett, WP ;
Merriam, WG ;
Ogunfusika, MO ;
Oser, SM ;
Harrington, AM ;
Shields, PG ;
Felley-Bosco, E ;
Hussain, SP ;
Harris, CC .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (01) :86-88
[2]  
Ambs S, 1998, CANCER RES, V58, P334
[3]  
Arrigo AP, 1998, BIOL CHEM, V379, P19
[4]   Are myoepithelial cells responsible for the widespread expression of inducible nitric oxide synthase in pleomorphic adenoma? An immunohistochemical study [J].
Brennan, PA ;
Umar, T ;
Zaki, GA ;
Langdon, JD ;
Spedding, A ;
Buckley, J ;
Downie, IP .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2000, 29 (06) :279-283
[5]   p53 accumulation in apoptotic macrophages is an energy demanding process that precedes cytochrome c release in response to nitric oxide [J].
Brockhaus, F ;
Brüne, B .
ONCOGENE, 1999, 18 (47) :6403-6410
[6]   Nitric oxide (NO):: an effector of apoptosis [J].
Brüne, B ;
von Knethen, A ;
Sandau, KB .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (10) :969-975
[7]   The Hsp70 and Hsp60 chaperone machines [J].
Bukau, B ;
Horwich, AL .
CELL, 1998, 92 (03) :351-366
[8]   ANALYSIS OF HEAT-SHOCK PROTEIN EXPRESSION IN MYELOID-LEUKEMIA CELLS BY FLOW-CYTOMETRY [J].
CHANT, ID ;
ROSE, PE ;
MORRIS, AG .
BRITISH JOURNAL OF HAEMATOLOGY, 1995, 90 (01) :163-168
[9]   HEAT-SHOCK PROTEIN-HSP70 IN PATIENTS WITH AXILLARY LYMPH NODE-NEGATIVE BREAST-CANCER - PROGNOSTIC IMPLICATIONS [J].
CIOCCA, DR ;
CLARK, GM ;
TANDON, AK ;
FUQUA, SAW ;
WELCH, WJ ;
MCGUIRE, WL .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) :570-574
[10]  
Cornford PA, 2000, CANCER RES, V60, P7099