Immunohistochemical assessment of Viadent®-associated leukoplakia

被引:15
作者
Anderson, KM
Stoner, GD
Fieds, HW
Chacon, GE
Dohar, AL
Gregg, BR
Mallery, SR
机构
[1] Univ Tennessee, Dept Biol & Diagnost Sci, Coll Dent, Memphis, TN 38163 USA
[2] Amer Canc Soc, Ohio Div, Dublin, OH 43017 USA
[3] Ohio State Univ, Lucius Wing Endowed Chair, Dept Internal Med, Div Hematol & Oncol,James Canc Ctr, Columbus, OH 43210 USA
[4] Ohio State Univ, Coll Dent, Dept Orthodont, Columbus, OH 43210 USA
[5] Ohio State Univ, Coll Dent, Dept Oral Maxillofacial Surg & Pathol, Columbus, OH 43210 USA
关键词
bioactivation; carcinogen; immunohistochemistry; leukoplakia; mutagen; Phase I and II enzymes; sanguinarine; xenobiotics;
D O I
10.1016/j.oraloncology.2004.08.008
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Studies show an association between sanguinarine, the active ingredient in Viadent((R)) oral health care products, and oral premalignant lesions. The study was undertaken to quantitatively compare the staining profiles of sanguinarine-associated leukoplakia to normal and dysplastic specimens. Archived oral mucosal specimens were stained for tumor markers p16, p53, cyclin D1, Ki-67, and Bcl-x and analyzed through Simple PCl(R) image analysis software. Quantitative analyses showed trends towards intermediate staining in Viadent((R))-related specimens (Ki-67: normal: 18.12 +/- 2.15, Viaden((R)): 16.12 +/- 2.16, dysplasia: 14.53 +/- 2.04, p > 0.05; cyclin D1: normal: 15.65 +/- 3.68, Viadent((R)): 12.52 +/- 3.57, dysplasia: 1.94 +/- 3.93, p < 0.05; p16: normal: 55.04 +/- 4.16, Viadent((R)): 49.74 +/- 4.16, dysptasia: 45.03 +/- 4.45; p > 0.05; p53:normal: 2.65 +/- 0.37, Viadent((R)): 4.64 +/- 1.52, dysplasia: 8.71 +/- 1.37; p < 0.05 Kruskal Wallace, Tukey/Kramer). Our Viadent profiles, intermediate between normal and dysplasia, support a preneoplastic nature of this process. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:200 / 207
页数:8
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