Assessment of MDM2 Gene Locus Amplification by Fluorescence In-Situ Hybridization in Juvenile Ossifying Fibroma.

IF 3.2 Q2 PATHOLOGY
Faraj Alotaiby, Saja A Alramadhan, Sarah G Fitzpatrick, Mohammed N Islam, Donald M Cohen, Indraneel Bhattacharyya
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Abstract

Juvenile ossifying fibroma (JOF) is an uncommon benign fibro-osseous lesion (BFOL) of the maxillofacial bones with a locally aggressive nature and a high recurrence rate. Murine Double Minute 2 (MDM2) is an oncogene located at chromosome 12 (12q13-15) that inhibits the tumor suppressor gene TP53. The presence of MDM2 gene locus amplification is a useful molecular adjunct in the evaluation of some sarcomas, including low-grade intramedullary osteosarcoma (LGIOS). JOF and LGIOS have some overlapping clinical and histopathological features. The aim of this study is to evaluate a series of JOF for the presence of MDM2 gene locus amplification using fluorescence in-situ hybridization (FISH).

Materials and methods: With IRB approval, a search of the institutional files of the archives of the Oral Pathology and Surgical Pathology biopsy services at the University of Florida Health was performed. The cases were re-evaluated by an oral pathology resident, an oral and maxillofacial pathologist, and a bone and soft tissue pathologist. Cases with consensus in diagnosis were selected (n = 9) for MDM2 testing. Testing by FISH for MDM2 gene locus amplification was applied to all retrieved cases.

Results: The examined cases were all negative for MDM2 gene locus amplification via FISH testing.

Conclusion: In our small series, JOF did not demonstrate MDM2 gene locus abnormality, a characteristic of LGIOS. This finding suggests that JOF has a distinct underlying pathogenesis. If confirmed in a larger series, these findings may be useful in distinguishing these two entities in cases with overlapping features or when minimal biopsy material is available.

通过荧光原位杂交评估幼年骨化性纤维瘤的 MDM2 基因座扩增情况
幼年骨化性纤维瘤(JOF)是一种不常见的颌面骨良性纤维骨病变(BFOL),具有局部侵袭性和高复发率。Murine Double Minute 2(MDM2)是位于第 12 号染色体(12q13-15)上的一种癌基因,可抑制抑癌基因 TP53。在评估某些肉瘤(包括低级别髓内骨肉瘤(LGIOS))时,MDM2基因位点扩增是一个有用的分子辅助指标。JOF 和 LGIOS 在临床和组织病理学特征上有一些重叠之处。本研究旨在利用荧光原位杂交(FISH)技术评估一系列JOF是否存在MDM2基因位点扩增:经 IRB 批准,对佛罗里达大学医疗中心口腔病理学和外科病理学活检服务档案中的机构档案进行了搜索。一名口腔病理学住院医师、一名口腔颌面病理学家和一名骨与软组织病理学家对病例进行了重新评估。筛选出诊断一致的病例(n = 9)进行 MDM2 检测。对所有检索到的病例进行MDM2基因位点扩增的FISH检测:结果:经 FISH 检测,所有病例的 MDM2 基因位点扩增均为阴性:结论:在我们的小样本病例中,JOF未显示MDM2基因位点异常,而MDM2基因位点异常是LGIOS的一个特征。这一发现表明,JOF 有其独特的潜在发病机制。如果在更大的系列中得到证实,这些发现可能有助于在特征重叠的病例中或在活检材料极少的情况下区分这两种实体。
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来源期刊
CiteScore
5.70
自引率
9.50%
发文量
99
期刊介绍: Head & Neck Pathology presents scholarly papers, reviews and symposia that cover the spectrum of human surgical pathology within the anatomic zones of the oral cavity, sinonasal tract, larynx, hypopharynx, salivary gland, ear and temporal bone, and neck. The journal publishes rapid developments in new diagnostic criteria, intraoperative consultation, immunohistochemical studies, molecular techniques, genetic analyses, diagnostic aids, experimental pathology, cytology, radiographic imaging, and application of uniform terminology to allow practitioners to continue to maintain and expand their knowledge in the subspecialty of head and neck pathology. Coverage of practical application to daily clinical practice is supported with proceedings and symposia from international societies and academies devoted to this field. Single-blind peer review The journal follows a single-blind review procedure, where the reviewers are aware of the names and affiliations of the authors, but the reviewer reports provided to authors are anonymous. Single-blind peer review is the traditional model of peer review that many reviewers are comfortable with, and it facilitates a dispassionate critique of a manuscript.
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