Pillai M R, Phanidhara A, Kesari A L, Nair P, Nair M K
Division of Laboratory Medicine, Regional Cancer Centre, Thiruvananthapuram, India.
J Surg Oncol. 1999 May;71(1):10-5. doi: 10.1002/(sici)1096-9098(199905)71:1<10::aid-jso3>3.0.co;2-v.
Human papillomavirus infection has been suggested to play a role in the development of epithelial carcinomas, particularly those of the uterine cervix. Less information is available on the role of the virus in oral lesions. It has been proposed that the viral oncoproteins specifically complex with the products of cellular tumor suppressor gene, namely E6 with p53 and E7 with retinoblastoma gene product. Inactivation or mutation in p53 gene is also known to result in loss of control over the cell cycle and increases in tumor proliferation rates. The present study examines the role of HPV infection in relation to p53 and the extent of the tumor proliferative compartment reflected by cyclin D1 and Ki-67 expression during various phases of tumor progression in the oral epithelium.
Nonisotopic in situ hybridization (NISH) was performed to detect HPV 6/11 and 16/18. Expression of p53, cyclin D1, Ki-67, and the HPV 16/18 E6 protein were detected by immunocytochemistry.
There was significant correlation between the extent of histological abnormality and HPV infection. A correlation (r = 0.250, P = 0.0089) was evident between the presence of HPV 16 and occurrence of invasive cancer. Expression of the tumor suppressor p53 protein also showed significant positive correlation with histology (r = 0.475, P = 0.00004). The tumor proliferative fraction also increased with the extent of histological abnormality (r = 0.387, P = 0.0003 for cyclin D1 and r = 0.463, P = 0.0001 for Ki 67). Accumulation of p53 and increase in tumor proliferation also correlated to the presence of HPV infection (r = 0.511, P = 0.00003 for p53; r = 0.478, P = 0.00002 for cyclin D1 and r = 0.521, P = 0.00004 for Ki-67).
The present study thus demonstrates the importance of HPV infection in oral tissue. Expression of the high-risk HPV 16/18 E6 protein also appears to be a critical event along with aberrant p53 expression. These results are of significance to the molecular epidemiology of oral cancer and may also be used to supplement and elaborate the diagnosis of oral lesions.
有人提出人乳头瘤病毒感染在上皮癌,尤其是子宫颈癌的发生过程中起作用。关于该病毒在口腔病变中的作用,人们了解较少。有人提出病毒癌蛋白与细胞肿瘤抑制基因的产物特异性结合,即E6与p53结合,E7与视网膜母细胞瘤基因产物结合。已知p53基因的失活或突变会导致对细胞周期控制的丧失以及肿瘤增殖率的增加。本研究探讨了人乳头瘤病毒感染与p53的关系,以及在口腔上皮肿瘤进展的各个阶段,细胞周期蛋白D1和Ki-67表达所反映的肿瘤增殖区室的范围。
采用非同位素原位杂交(NISH)检测人乳头瘤病毒6/11和16/18。通过免疫细胞化学检测p53、细胞周期蛋白D1、Ki-67和人乳头瘤病毒16/18 E6蛋白的表达。
组织学异常程度与HPV感染之间存在显著相关性。HPV 16的存在与浸润性癌的发生之间存在明显的相关性(r = 0.250,P = 0.0089)。肿瘤抑制蛋白p53的表达与组织学也显示出显著的正相关性(r = 0.475,P = 0.00004)。肿瘤增殖分数也随着组织学异常程度的增加而增加(细胞周期蛋白D1的r = 0.387,P = 0.0003;Ki-67的r = 0.463,P = 0.0001)。p53的积累和肿瘤增殖的增加也与HPV感染的存在相关(p53的r = 0.511,P = 0.00003;细胞周期蛋白D1的r = 0.478,P = 0.00002;Ki-67的r = 0.521,P = 0.00004)。
本研究因此证明了HPV感染在口腔组织中的重要性。高危人乳头瘤病毒16/18 E6蛋白的表达以及异常的p53表达似乎也是关键事件。这些结果对于口腔癌的分子流行病学具有重要意义,也可用于补充和完善口腔病变的诊断。