Tammewar Suvidha, Gadkari Rasika
Department of Pathology, Datta Meghe Institute of Medical Sciences, Sawangi, Wardha, Maharashtra, India.
Department of Pathology, All India Institute of Medical Sciences, Nagpur, Maharashtra, India.
J Cytol. 2022 Apr-Jun;39(2):53-58. doi: 10.4103/joc.joc_198_21. Epub 2022 May 20.
The present study evaluated the frequency of micronuclei in oral potentially malignant disorders (OPMDs) and their association with the presence of dysplasia on cytology and biopsy as well as their association with p53 mutation and p16 expression. Cytological findings of dysplastic changes in OPMDs were compared to histological diagnoses.
This was a cross-sectional, observational, descriptive study. Scrape smears ( = 74) were collected from lesions in patients with OPMDs. Punch biopsy was collected in patients showing dysplastic changes. Tissue microarray for p53 mutation and p16 expression was performed using paraffin embedded blocks. Cases were classified into grades of dysplasia using both scrape smears and biopsy. Micronuclei frequency was calculated per 100 cells using scrape smears. Mann-Whitney U test was used for correlation of cytology and histology for grade of dysplasia as well as micronuclear frequency with p53 mutation and p16 expression.
Micronuclear frequency was found to be increased in patients with dysplasia. A significant association of micronuclear frequency with dysplastic changes was seen on cytology. Sensitivity of cytological evaluation was found to be 64.7%. The association of the micronuclear frequency of samples with p53 mutation and p16 expression was nearly significant (n = 28, = 0.069 and 0.095, respectively).
Micronuclear frequency can be a reliable marker of mutagenic change in OPMDs. Cytological assessment of micronuclei can serve as useful, non-invasive, and relatively inexpensive tool to predict cancerous changes in OPMDs.
本研究评估口腔潜在恶性疾病(OPMDs)中微核的频率,及其与细胞学和活检中发育异常的存在之间的关联,以及与p53突变和p16表达的关联。将OPMDs中发育异常变化的细胞学结果与组织学诊断进行比较。
这是一项横断面、观察性、描述性研究。从OPMDs患者的病变处收集刮片(n = 74)。对显示发育异常变化的患者进行钻取活检。使用石蜡包埋块进行p53突变和p16表达的组织微阵列检测。使用刮片和活检将病例分为发育异常等级。使用刮片计算每100个细胞中的微核频率。采用Mann-Whitney U检验分析发育异常等级的细胞学与组织学相关性,以及微核频率与p53突变和p16表达的相关性。
发现发育异常患者的微核频率增加。在细胞学上,微核频率与发育异常变化之间存在显著关联。细胞学评估的敏感性为64.7%。样本的微核频率与p53突变和p16表达的关联接近显著(n = 28,P分别为0.069和0.095)。
微核频率可作为OPMDs中诱变变化的可靠标志物。微核的细胞学评估可作为预测OPMDs癌变变化的有用、非侵入性且相对廉价的工具。