4NQO CARCINOGENESIS - A MOUSE MODEL OF ORAL CAVITY SQUAMOUS-CELL CARCINOMA

被引:117
作者
HAWKINS, BL
HENIFORD, BW
ACKERMANN, DM
LEONBERGER, M
MARTINEZ, SA
HENDLER, FJ
机构
[1] JAMES GRAHAM BROWN CANC CTR,DEPT SURG,LOUISVILLE,KY 40292
[2] JAMES GRAHAM BROWN CANC CTR,DEPT PATHOL,LOUISVILLE,KY 40292
[3] JAMES GRAHAM BROWN CANC CTR,DEPT MED,LOUISVILLE,KY 40292
[4] JAMES GRAHAM BROWN CANC CTR,DEPT BIOCHEM,LOUISVILLE,KY 40292
[5] UNIV LOUISVILLE,LOUISVILLE VET AFFAIRS MED CTR,LOUISVILLE,KY 40292
[6] ALLIANT HOSP,LOUISVILLE,KY
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 1994年 / 16卷 / 05期
关键词
D O I
10.1002/hed.2880160506
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. A murine model of oral cavity carcinogenesis is needed to study the molecular aspects of malignant transformation. 4-Nitroquinoline-1-oxide (4NQO), a water-soluble carcinogen, produces squamous cell carcinoma in rodents. Protocols were designed to investigate the temporal aspects of neoplastic transformation. Methods. 4NQO was applied topically to mouse palates for up to 16 weeks. Mice were observed and killed from 24 to 49 weeks, Results. A spectrum of lesions ranging from atypia to moderately differentiated invasive squamous cell carcinoma (SCC) was produced. The severity of the lesions corresponded to the duration of treatment and the length of observation. There was no gross or microscopic evidence of an inflammatory reaction to 4NQO. The lesions were focal and normal mucosa predominated in the treated mice. Conclusion. 4NQO reliably produced preneoplastic and malignant oral cavity lesions, which morphologically and histologically mimic human head and neck cancer. Lesions develop long after 4NQO exposure and without an inflammatory response. Thus, the model should be useful for molecular analysis of neoplastic transformation. (C) 1994 John Wiley & Sons, Inc.
引用
收藏
页码:424 / 432
页数:9
相关论文
共 20 条
[1]  
BAKER SR, 1986, OTOLARYNGOLOGY HEAD, P1281
[2]  
BROWN K, 1990, P NATL ACAD SCI USA, V87, P2403
[3]  
EVERSON JW, 1981, J ORAL PATHOL, V10, P129
[4]  
FUJINO H, 1965, J NATL CANCER I, V35, P907
[5]  
HENDLER FJ, 1989, CANCER CEL, V7, P347
[6]   VARIATION IN CELLULAR EGF RECEPTOR MESSENGER-RNA EXPRESSION DEMONSTRATED BY IN-SITU REVERSE-TRANSCRIPTASE POLYMERASE CHAIN-REACTION [J].
HENIFORD, BW ;
SHUMSIU, A ;
LEONBERGER, M ;
HENDLER, FJ .
NUCLEIC ACIDS RESEARCH, 1993, 21 (14) :3159-3166
[7]  
NAKAHARA W, 1957, Gan, V48, P129
[8]   THE N-2-GUANINE ADDUCT BUT NOT THE C8-GUANINE OR N-6-ADENINE ADDUCTS FORMED BY 4-NITROQUINOLINE 1-OXIDE BLOCKS THE 3'-5' EXONUCLEASE ACTION OF T4 DNA-POLYMERASE [J].
PANIGRAHI, GB ;
WALKER, IG .
BIOCHEMISTRY, 1990, 29 (08) :2122-2126
[9]   SUBJECTIVITY IN EVALUATING ORAL EPITHELIAL DYSPLASIA, CARCINOMA INSITU AND INITIAL CARCINOMA [J].
PINDBORG, JJ ;
REIBEL, J ;
HOLMSTRUP, P .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1985, 14 (09) :698-708
[10]   ORAL EPITHELIAL ATYPIA AND ACANTHOLYTIC DYSKERATOSIS IN RATS PAINTED WITH 4-NITROQUINOLINE N-OXIDE [J].
PRIME, SS ;
MALAMOS, D ;
ROSSER, T ;
SCULLY, C .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1986, 15 (05) :280-283