The mRNA expression of inducible nitric oxide synthase in DMBA-induced hamster buccal-pouch carcinomas:: an in situ RT-PCR study

被引:7
作者
Chen, YK [1 ]
Hsu, SS [1 ]
Lin, LM [1 ]
机构
[1] Kaohsiung Med Univ, Sch Dent, Dept Oral Pathol, Kaohsiung, Taiwan
关键词
DMBA-carcinogenesis; hamster; inducible nitric oxide synthase; mRNA; in situ reverse transcription-polymerase chain reaction;
D O I
10.1046/j.1365-2613.2002.00222.x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Three isoforms of nitric oxide synthase (NOS) have been identified: endothelial NOS, neuronal NOS, and inducible NOS (iNOS). The enhanced expression of iNOS at the protein level using immunohistochemical technique has been reported previously in chemically induced oral carcinomas in hamster buccal-pouch mucosa. However, the corresponding expression of iNOS at the mRNA level has not yet been demonstrated using in situ reverse transcription-polymerase chain reaction (IS RT-PCR). The purpose of the present study is to assess the iNOS mRNA expression level in 7,12-dimethylbenz[a]anthracene (DMBA)-induced hamster buccal-pouch carcinomas using IS RT-PCR. Thirty outbred, young (6-weeks old), male, Syrian golden hamsters (Mesocricatus auratus ) were randomly divided into one experimental group (10 animals), and two control groups (10 animals each). The pouches of a group of 10 animals of the experimental group were painted bilaterally with a 0.5% DMBA solution three times a week for 15 weeks. Each animal of one of the control groups was similarly treated with only mineral oil. Another control group of 10 animals remained untreated throughout the experiment. Invasive squamous-cell carcinomas with a 100% tumour incidence developed in all of the DMBA-treated buccal pouches. The mineral oil-treated and untreated pouches revealed no obvious changes. Inducible NOS mRNA was demonstrated amongst all the 15-week DMBA-treated hamster buccal-pouch mucosa animals, but not in the untreated animals and not in the animals for which the buccal-pouch was treated with mineral oil. Further study is necessary to evaluate the mechanism(s) which contribute to the increased iNOS mRNA expression for experimentally induced oral carcinogenesis.
引用
收藏
页码:133 / 137
页数:5
相关论文
共 18 条
  • [1] Ambs S, 1998, CANCER RES, V58, P334
  • [2] Expression of inducible nitric oxide synthase and p53 in oral epithelial dysplasia
    Brennan, PA
    Conroy, B
    Spedding, AV
    [J]. ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTOLOGY, 2000, 90 (05): : 624 - 629
  • [3] Correlation between type II nitric oxide synthase and p53 expression in oral squamous cell carcinoma
    Brennan, PA
    Palacios-Callender, M
    Umar, T
    Hughes, D
    Spedding, AV
    Zaki, GA
    Langdon, JD
    [J]. BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 2000, 38 (06) : 627 - 632
  • [4] Sequential expression of placental glutathione S-transferase (GST-P) during DMBA-induced hamster buccal pouch squamous cell carcinogenesis
    Chen, YK
    Lin, LM
    [J]. JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1996, 25 (07) : 388 - 394
  • [5] Immunohistochemical expression of inducible nitric oxide synthase in DMBA-induced hamster buccal pouch carcinogenesis
    Chen, YK
    Lin, LM
    [J]. ORAL ONCOLOGY, 2000, 36 (02): : 221 - 224
  • [6] D'Ambrosio SM, 2001, ENVIRON MOL MUTAGEN, V37, P46, DOI 10.1002/1098-2280(2001)37:1<46::AID-EM1005>3.0.CO
  • [7] 2-6
  • [8] GIMENEZCONTI IB, 1993, J CELL BIOCHEM, P83
  • [9] HEVEL JM, 1991, J BIOL CHEM, V266, P22789
  • [10] Klotz T, 1998, CANCER, V82, P1897, DOI 10.1002/(SICI)1097-0142(19980515)82:10<1897::AID-CNCR12>3.0.CO