Chang Kong-Chao, Su Ih-Jen, Tsai Sen-Tien, Shieh Dar-Bin, Jin Ying-Tai
Department of Pathology, National Cheng University Medical Center, Tainan, Taiwan.
Oncology. 2002;63(4):362-9. doi: 10.1159/000066227.
Betel quid (BQ) chewing has been a well-documented cause of oral epithelial lesions (OEL). Evolution from early hyperplastic lesions to the late or carcinomatous stage has been recognized. The pathobiological and molecular mechanism, however, remains to be elucidated. In this study, a total of 232 samples obtained from 153 cases of BQ-related OEL were retrospectively evaluated for the expression of p53 and bcl-2 in comparison with 26 cases of BQ-unrelated lesions (n = 29). The possible role of human papillomavirus (HPV) was also investigated. These BQ-related OELs included verrucous hyperplasia (VIH, n = 57, 24.6%), epithelial dysplasia (n = 23, 9.9%), verrucous carcinoma (VC, n = 5, 2.1%) and squamous cell carcinoma (SCC, n = 106, 45.7%). Fifty-four cases (35.3%) had multiple lesions. In comparison with the BQ-unrelated OELs, the characteristics of BQ-related OELs were a younger age, male predilection and multicentricity. In contrast to the tongue in BQ-unrelated OELs, the most common site for all types of BQ-related lesions was the buccal mucosa. Immunohistochemical studies of BQ-related lesions showed p53 staining in 30% of dysplasia and 38% of SCC, but a consistent absence in VH and VC. The cases with p53-positive SCC had a higher recurrence rate than p53-negative ones. Bcl-2 expression was negligible for all types of lesions. HPV-6/11 was detectable in 10% of dysplasia and 13% of SCC, but in neither VH nor VC. HPV-16/18, however, was consistently negative for all types of lesions. Our data suggest that p53, but not bcl-2, may play a role in tumor progression of BQ-related OELs, and that VH and VC are distinct and closely related histological lesions. The consistent absence of the malignant-type HPV in all BQ-related lesions suggests that HPV plays an insignificant role in the tumorigenesis of BQ-related oral cancers, although a cooperative role may exist between the benign-type HPV and BQ chewing.
嚼槟榔(BQ)是口腔上皮病变(OEL)的一个已被充分记录的病因。从早期增生性病变发展到晚期或癌变阶段已得到公认。然而,其病理生物学和分子机制仍有待阐明。在本研究中,回顾性评估了从153例与BQ相关的OEL中获取的总共232个样本中p53和bcl-2的表达情况,并与26例与BQ无关的病变(n = 29)进行了比较。还研究了人乳头瘤病毒(HPV)的可能作用。这些与BQ相关的OEL包括疣状增生(VIH,n = 57,24.6%)、上皮发育异常(n = 23,9.9%)、疣状癌(VC,n = 5,2.1%)和鳞状细胞癌(SCC,n = 106,45.7%)。54例(35.3%)有多处病变。与与BQ无关的OEL相比,与BQ相关的OEL的特征是年龄较轻、男性居多且多中心性。与与BQ无关的OEL中舌部为最常见部位不同,所有类型与BQ相关病变最常见的部位是颊黏膜。对与BQ相关病变的免疫组织化学研究显示,在30%的发育异常和38%的SCC中p53呈阳性染色,但在VH和VC中始终未检测到。p53阳性SCC病例的复发率高于p53阴性病例。所有类型病变中bcl-2的表达均微不足道。在10%的发育异常和13%的SCC中可检测到HPV-6/11,但在VH和VC中均未检测到。然而,所有类型病变中HPV-16/18始终为阴性。我们的数据表明,p53而非bcl-2可能在与BQ相关的OEL的肿瘤进展中起作用,并且VH和VC是不同但密切相关的组织学病变。所有与BQ相关病变中均始终未检测到恶性型HPV,这表明HPV在与BQ相关的口腔癌的肿瘤发生中作用不大,尽管良性型HPV与嚼槟榔之间可能存在协同作用。