Immunohistochemical demonstration of p73 protein in the early stages of DMBA-induced squamous-cell carcinogenesis in hamster buccal pouch

被引:11
作者
Chen, YK [1 ]
Hsue, SS [1 ]
Lin, LM [1 ]
机构
[1] Kaohsiung Med Univ, Sch Dent, Dept Oral Pathol, Kaohsiung, Taiwan
关键词
p73; DMBA carcinogenesis; hamster;
D O I
10.1016/S0003-9969(02)00054-7
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The identification of a new protein, p73, with structural and functional similarities to p53 protein suggests that a family of p53-like proteins is likely to exist. This study investigated the status of p73 protein in the early stages of 7,12-dimethyl benz[a]anthracene (DMBA)-induced carcinogenesis. Outbred young (6-week-old) male Syrian golden hamsters (Mesocricatus auratus; 40 animals) were randomly divided into four equal groups: a 3-week DMBA-treated experimental group, a 6-week DMBA-treated experimental group, a mineral oil-treated control group, and a non-treated control group. Following this, a total of 80 specimens of pouch mucosa were obtained from the 40 animals in the four groups. Positive nuclear staining for p73 protein was randomly distributed throughout the whole epithelial layer of the DMBA-treated specimens and was absent in controls. Positive p73 staining was observed in 8 of the 20 (40%) 3-week, and 14 of the 20 (70%) 6-week DMBA-treated specimens. None of the 3-week DMBA-treated specimens revealed more than 25% p73-positive keratinocytes, but, in 12 (60%) of the 6-week-treated specimens, more than 25% of the keratinocytes examined were p73-positive. This suggests that the longer the DMBA painting period, the higher the proportion of p73-stained pouch keratinocytes. Furthermore, a p73-dependent mechanism may be associated with the early stages of oral carcinogenesis. Such a mechanism could be very important to an understanding of the participation of p73 in the development of oral squamous-cell carcinomas. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:695 / 699
页数:5
相关论文
共 17 条
[1]  
AHOMADEGBE JC, 1995, ONCOGENE, V10, P1217
[2]   Tumour-suppressor genes - Killer in search of a motive? [J].
Clurman, B ;
Groudine, M .
NATURE, 1997, 389 (6647) :122-123
[3]   P73 expression in basal layers of head and neck squamous epithelium:: a role in differentiation and carcinogenesis in concert with p53 and p63? [J].
Fardioni-Laurens, L ;
Bosq, J ;
Janot, F ;
Vayssade, M ;
Le Bihan, ML ;
Kaghad, M ;
Caput, D ;
Bénard, J ;
Ahomadegbe, JC .
ONCOGENE, 2001, 20 (38) :5302-5312
[4]  
GIMENEZCONTI IB, 1993, J CELL BIOCHEM, P83
[5]   P53 IN TUMOR PATHOLOGY - CAN WE TRUST IMMUNOHISTOCHEMISTRY - REVISITED [J].
HALL, PA ;
LANE, DP .
JOURNAL OF PATHOLOGY, 1994, 172 (01) :1-4
[6]   CLINICAL IMPLICATIONS OF THE P53 TUMOR-SUPPRESSOR GENE [J].
HARRIS, CC ;
HOLLSTEIN, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (18) :1318-1327
[7]   USE OF AVIDIN-BIOTIN-PEROXIDASE COMPLEX (ABC) IN IMMUNOPEROXIDASE TECHNIQUES - A COMPARISON BETWEEN ABC AND UNLABELED ANTIBODY (PAP) PROCEDURES [J].
HSU, SM ;
RAINE, L ;
FANGER, H .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1981, 29 (04) :577-580
[8]   p73 is a human p53-related protein that can induce apoptosis [J].
Jost, CA ;
Marin, MC ;
Kaelin, WG .
NATURE, 1997, 389 (6647) :191-194
[9]   The p53 gene family [J].
Kaelin, WG .
ONCOGENE, 1999, 18 (53) :7701-7705
[10]   Monoallelically expressed gene related to p53 at 1p36, a region frequently deleted in neuroblastoma and other human cancers [J].
Kaghad, M ;
Bonnet, H ;
Yang, A ;
Creancier, L ;
Biscan, JC ;
Valent, A ;
Minty, A ;
Chalon, P ;
Lelias, JM ;
Dumont, X ;
Ferrara, P ;
McKeon, F ;
Caput, D .
CELL, 1997, 90 (04) :809-819