Involvement of viral and chemical factors with oral cancer in Taiwan

被引:44
作者
Yang, YY
Koh, LW
Tsai, JH
Tsai, CH
Wong, EFC
Lin, SJ
Yang, CC
机构
[1] Chung Shan Med Univ, Sch Med Technol, Taichung 402, Taiwan
[2] Show Chwan Mem Hosp, Dept Med Res, Changhua, Taiwan
[3] Show Chwan Mem Hosp, Dept Obstet & Gynecol, Changhua, Taiwan
[4] Chung Shan Med Univ Hosp, Dept Surg, Taichung, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Pathol, Taichung, Taiwan
关键词
oral cancer; virus; arecoline;
D O I
10.1093/jjco/hyh037
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The association between oral squamous cell carcinoma (OSCC) and viral and chemical factors is uncertain. Therefore the correlation of viral and chemical factors with oral cancer in Taiwan was investigated. Methods: Thirty-seven paraffin-em bedded oral cancer biopsies and 36 normal oral tissue specimens were examined by the polymerase chain reaction method for six viruses: HPV, CMV, EBV, HSV-1, HSV-2 and HHV-8. To elucidate the role of arecoline in the oncogenesis of oral cancer, human buccal fibroblasts, oral submucosal fibroblasts and three cancer cell lines KB, GNM and TSCCa were used for MTT cytotoxity assay and flow cytometry DNA content analysis. Results: Two (5.4%) HSV-1-positive and four (10.8%) HPV-positive cases were recognized in oral cancer biopsies. Among the four HPV-positive tissues, two were further typed as HPV-16, one was identified as HPV-18- and HSV-1-positive; and one contained both HPV-16 and HPV-18. One sample presented HSV-1 only. Arecoline, at a concentration lower than 0.8 mug/ml, increased cell growth (all cell types); at higher concentrations (25-400 mug/ml) it was cytotoxic. The cell cycle was demonstrated to be altered either by low or high concentrations of arecoline treatment, depending on the cells treated. Conclusions: The data demonstrated that HPV, HSV-1 and betel quid chewing were significantly associated with OSCC, but HSV-2, CMV, EBV and HHV-8 were not. We suggest that the most determinative factor for oral cancer may be chemical in nature rather than viral infection.
引用
收藏
页码:176 / 183
页数:8
相关论文
共 29 条
[1]  
ASHBY J, 1979, LANCET, V1, P112
[2]   GENITAL HUMAN PAPILLOMAVIRUS INFECTION IN FEMALE UNIVERSITY-STUDENTS AS DETERMINED BY A PCR-BASED METHOD [J].
BAUER, HM ;
TING, Y ;
GREER, CE ;
CHAMBERS, JC ;
TASHIRO, CJ ;
CHIMERA, J ;
REINGOLD, A ;
MANOS, MM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (04) :472-477
[3]   HIGH PREVALENCE OF HUMAN PAPILLOMAVIRUS INFECTION AND POSSIBLE ASSOCIATION WITH BETEL QUID CHEWING AND SMOKING IN ORAL EPIDERMOID CARCINOMAS IN TAIWAN [J].
CHANG, KW ;
CHANG, CS ;
LAI, KS ;
CHOU, MJ ;
CHOO, KB .
JOURNAL OF MEDICAL VIROLOGY, 1989, 28 (01) :57-61
[4]   IDENTIFICATION OF HERPESVIRUS-LIKE DNA-SEQUENCES IN AIDS-ASSOCIATED KAPOSIS-SARCOMA [J].
CHANG, Y ;
CESARMAN, E ;
PESSIN, MS ;
LEE, F ;
CULPEPPER, J ;
KNOWLES, DM ;
MOORE, PS .
SCIENCE, 1994, 266 (5192) :1865-1869
[5]   Risk of oral cancer associated with human papillomavirus infection, betel quid chewing, and cigarette smoking in Taiwan - an integrated molecular and epidemiological study of 58 cases [J].
Chen, PCH ;
Kuo, C ;
Pan, CC ;
Chou, MY .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2002, 31 (06) :317-322
[6]   Biotinyl-tyramide-based in situ hybridization signal patterns distinguish human papillomavirus type and grade of cervical intraepithelial neoplasia [J].
Evans, MF ;
Mount, SL ;
Beatty, BG ;
Cooper, K .
MODERN PATHOLOGY, 2002, 15 (12) :1339-1347
[7]   CANCER CAUSES REVISITED - HUMAN PAPILLOMAVIRUS AND CERVICAL NEOPLASIA [J].
FRANCO, EL .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (11) :779-780
[8]  
HAMILTONDUTOIT SJ, 1991, AM J PATHOL, V138, P149
[9]   RELATION OF BURKITTS TUMOR-ASSOCIATED HERPES-TYPE VIRUS TO INFECTIOUS MONONUCLEOSIS [J].
HENLE, G ;
HENLE, W ;
DIEHL, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 59 (01) :94-&
[10]   GENOTOXIC AND NONGENOTOXIC EFFECTS OF BETEL QUID INGREDIENTS ON ORAL MUCOSAL FIBROBLASTS IN-VITRO [J].
JENG, JH ;
KUO, ML ;
HAHN, LJ ;
KUO, MYP .
JOURNAL OF DENTAL RESEARCH, 1994, 73 (05) :1043-1049