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首页> 外文期刊>Advanced Biomedical Research >Stem Cell Markers SOX-2 and OCT-4 Enable to Resolve the Diagnostic Dilemma between Ameloblastic Carcinoma and Aggressive Solid Multicystic Ameloblastoma
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Stem Cell Markers SOX-2 and OCT-4 Enable to Resolve the Diagnostic Dilemma between Ameloblastic Carcinoma and Aggressive Solid Multicystic Ameloblastoma

机译:干细胞标记SOX-2和OCT-4能够解决成潮细胞癌和侵袭性固体多囊性成釉细胞瘤之间的诊断难题

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摘要

Background: Ameloblastic carcinoma (ACA) is a malignant neoplasm with overlapping histopathological features of benign aggressive solid multicystic ameloblastoma (SMA). This often leads to misdiagnosis with direct implication on the management protocol. The need of the hour is to adopt reliable tissue biomarkers to differentiate these lesions accurately that will help to implement an appropriate treatment modality. Few studies to differentiate ACA and SMA in literature with a limitation of a single marker and lack of availability of cases have prompted us to undertake this study. Thereby, this study is aimed at resolving the diagnostic dilemma in differentiating ACA and aggressive SMA using SOX-2, OCT-4 and CD44. Materials and Methods: Tissue samples involved 40 archival cases of histopathologically confirmed cases of ACA ( n = 20) and SMA ( n = 20). The sections were subjected to immunohistochemical staining using antibodies to SOX-2, OCT-4 and CD44. Nuclear staining for SOX-2 and OCT-4 and membranous reactivity for CD44 was considered positive. Results: The expression of SOX-2 and OCT-4 in ACA was statistically significant when compared to SMA ( P 0.001). CD44 showed an insignificant statistical value of 0.077 in differentiating ACA and SMA. SOX-2 and OCT-4 expression in ACA showed a significant correlation coefficient of 0.616 at P 0.004. Conclusions: SOX-2 and OCT-4 could serve as independent novel markers in resolving the diagnostic dilemma between ACA and aggressive SMA.
机译:背景:成虫细胞癌(ACA)是具有良性侵袭性实体多囊性成釉细胞瘤(SMA)的组织病理学特征重叠的恶性肿瘤。这通常会导致误诊,直接影响管理协议。一个小时的需要是采用可靠的组织生物标记物来准确区分这些病变,这将有助于实施适当的治疗方式。很少有研究能够在文献中区分ACA和SMA,而单一标记物的局限性和缺乏病例的可用性促使我们进行这项研究。因此,本研究旨在解决使用SOX-2,OCT-4和CD44区分ACA和侵袭性SMA的诊断难题。材料和方法:组织样本涉及40例经病理组织学确认为ACA(n = 20)和SMA(n = 20)的档案病例。使用抗SOX-2,OCT-4和CD44的抗体对切片进行免疫组织化学染色。 SOX-2和OCT-4的核染色以及CD44的膜反应性被认为是阳性的。结果:与SMA相比,ACA中SOX-2和OCT-4的表达具有统计学意义(P <0.001)。 CD44在区分ACA和SMA时显示的统计学值小于0.077。 ACA中SOX-2和OCT-4的表达在P <0.004时具有0.616的显着相关系数。结论:SOX-2和OCT-4可以作为独立的新标记物,解决ACA和侵袭性SMA之间的诊断难题。

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