Department of Oral & Maxillofacial Surgery, Soroka Medical Center, Beer Sheva, Israel.
Big Biomedical Data Research Laboratory, Hebrew University, Hadassah School of Dental Medicine, Jerusalem, Israel.
J Oral Pathol Med. 2020 Nov;49(10):1068-1077. doi: 10.1111/jop.13102. Epub 2020 Sep 14.
The stroma of odontogenic cysts/tumors may confer them differential biological behavior. We aimed to investigate the immunoexpression of stem cell markers (Nanog, SOX2, Oct4, and CD34) in the stroma of odontogenic cysts and tumors. CD34 was investigated exclusively as a marker for stromal fibroblast/fibrocyte cells (CD34 + SFCs). CD34 + SFCs were also investigated ultrastructurally.
Ten cases each of primary odontogenic keratocyst (OKC), recurrent OKC, dentigerous cyst, ameloblastoma, unicystic ameloblastoma, odontogenic myxoma, and 7 syndromic OKC were included. Results were represented as the mean score (%) of positive cells/field for each marker for each study group. For CD34 + SFCs, results are presented as the mean number of cells/field for each type of lesion. Kruskal-Wallis and Spearman's correlation statistical tests were used; significance was set at P < .05.
All markers except Oct4 were expressed by stromal cells in all lesions. Expression of SOX2 was significantly higher in tumors than in cysts (P < .05). CD34 + SFCs were more frequent in cysts than in tumors. Ultrastructurally, CD34 + SFCs were identified for the first time in odontogenic lesions and showed characteristic bipolar/dendritic morphology.
Among examined stromal stem cell markers, only SOX2 distinguished tumors from cysts. CD34 + SFCs may also contribute to the biological behavior of odontogenic lesions.
牙源性囊肿/肿瘤的基质可能赋予它们不同的生物学行为。我们旨在研究干细胞标志物(Nanog、SOX2、Oct4 和 CD34)在牙源性囊肿和肿瘤基质中的免疫表达。CD34 仅作为基质成纤维细胞/纤维细胞(CD34+SFCs)的标志物进行研究。还对 CD34+SFCs 进行了超微结构研究。
纳入原发性牙源性角化囊肿(OKC)、复发性 OKC、含牙囊肿、成釉细胞瘤、单囊型成釉细胞瘤、牙源性黏液瘤和 7 例综合征性 OKC 各 10 例。结果表示为每个标志物在每个研究组中的阳性细胞/视野的平均评分(%)。对于 CD34+SFCs,结果表示为每种病变的每个细胞/视野的平均数量。使用 Kruskal-Wallis 和 Spearman 相关统计检验;显著性水平设为 P<0.05。
除 Oct4 外,所有标志物均在所有病变的基质细胞中表达。SOX2 在肿瘤中的表达明显高于囊肿(P<0.05)。与肿瘤相比,囊肿中 CD34+SFCs 更为常见。超微结构上,首次在牙源性病变中鉴定出 CD34+SFCs,并表现出特征性的双极/树突状形态。
在所检查的基质干细胞标志物中,只有 SOX2 能区分肿瘤和囊肿。CD34+SFCs 也可能有助于牙源性病变的生物学行为。