McAlinden R L, Maxwell P, Napier S, Hamilton P, Cowan C G, Lundy F T, Lamey P J, Marley J J
School of Clinical Dentistry, The Queen's University of Belfast, Royal Group of Hospitals, Grosvenor Rd, Belfast BT12 6BP.
Oral Dis. 2000 Sep;6(5):318-26. doi: 10.1111/j.1601-0825.2000.tb00145.x.
To examine, for the first time Bcl-2 expression in sequential (autogenous) oral mucosal biopsies taken from the same sites in a gender, risk-factor matched, Caucasoid sample, over a 21-year period.
Retrospective immunocytochemical longitudinal study of archival serial biopsies.
Computer records were used to identify biopsy specimens derived from 12 patients. These were divided into four groups: (1) Histologically innocuous lesions which remained histologically innocuous. (2) Dysplastic lesions which remained dysplastic. (3) Histologically innocuous lesions which later progressed to squamous cell carcinoma (SCC). (4) Dysplastic lesions which later progressed to SCC. This represented 65 biopsies in total. Bcl-2 expression was studied using mouse antihuman BCL-2 oncoprotein clone 124 (Dako, Denmark).
Generally, there was a lack of Bcl-2 immunoreactivity in the epithelium, with one exception in dysplastic epithelium from a group (3) patient.
These findings suggest that in our series, Bcl-2 is not expressed early in oral premalignant lesions and appears to contradict previous reports. Possible explanations for this disparity are considered.
首次在一个性别、危险因素匹配的高加索样本中,对在21年期间从相同部位采集的连续(自体)口腔黏膜活检组织进行Bcl-2表达检测。
对存档系列活检组织进行回顾性免疫细胞化学纵向研究。
利用计算机记录识别来自12例患者的活检标本。这些标本被分为四组:(1)组织学上无害且一直保持无害的病变。(2)发育异常且一直保持发育异常的病变。(3)组织学上无害但后来进展为鳞状细胞癌(SCC)的病变。(4)发育异常但后来进展为SCC的病变。总共代表65次活检。使用小鼠抗人BCL-2癌蛋白克隆124(丹麦达科公司)研究Bcl-2表达。
一般来说,上皮细胞中缺乏Bcl-2免疫反应性,只有一名来自第(3)组患者的发育异常上皮细胞为例外。
这些发现表明,在我们的系列研究中,Bcl-2在口腔癌前病变早期不表达,这似乎与之前的报道相矛盾。文中考虑了这种差异的可能解释。