Sood Anubhuti, Mishra Deepika, Kharbanda Om Prakash, Chauhan Shyam S, Gupta Siddharth Datta, Deo Suryanarayana S V, Yadav Rahul, Ralhan Ranju, Kumawat Ramniwas, Kaur Harpreet
Department of Oral Pathology and Microbiology, Centre for Dental education and Research, All India Institute of Medical Sciences, Delhi, India.
Centre for Dental education and Research, All India Institute of Medical Sciences, Delhi, India.
J Oral Maxillofac Pathol. 2022 Apr-Jun;26(2):166-172. doi: 10.4103/jomfp.jomfp_402_20. Epub 2022 Jun 28.
S100 proteins have been implicated in the tumorigenesis of different human cancers and in oral dysplasia, as they are keratinocytes.
In the present study, we have attempted to compare the expression of S100-A7 within young-onset (age ≤45 years, Group 1) oral squamous cell carcinoma (OSCC), OSCC in older age groups (age >45 years Group 2), oral potentially malignant disorders (OPMDs, Group 3) and inflammatory lesions (Group 4). The tissue sections were scored based on the percentage of immunostained cells and staining intensity. Nuclear, cytoplasmic and membrane immunoreactivity were also scored.
The present study comprised 153 histopathologically diagnosed case subjects of OSCC >45 years ( = 41), OSCC <45 years ( = 36), OPMD ( = 40) and inflammatory lesions ( = 36). The present study revealed a statistically significant difference of distribution with regard to S100A7 staining (cytoplasmic and nuclear) between OPMDs and OSCC ( < 0.05). The nuclear, cytoplasmic and membrane staining as well as the staining intensity had significantly different scoring patterns among the OSCC group, OPMD group and the inflammatory lesions with the OSCC group having the highest scoring of the S100A7 staining (irrespective of the age).
The present study concludes that S100A7 can be used as a diagnostic biomarker to differentiate between OPMDs and OSCC lesions. However, the marker is unable to distinguish between OSCCs in younger and older patients as the molecular pathogenesis of tumors in either of these age groups is probably similar.
S100蛋白因其存在于角质形成细胞中,已被证实与不同人类癌症及口腔发育异常的肿瘤发生有关。
在本研究中,我们试图比较S100 - A7在年轻发病(年龄≤45岁,第1组)口腔鳞状细胞癌(OSCC)、老年组OSCC(年龄>45岁,第2组)、口腔潜在恶性疾病(OPMDs,第3组)和炎性病变(第4组)中的表达情况。根据免疫染色细胞的百分比和染色强度对组织切片进行评分。还对核、胞质和膜免疫反应性进行了评分。
本研究包括153例经组织病理学诊断的病例,其中年龄>45岁的OSCC患者41例,年龄<45岁的OSCC患者36例,OPMD患者40例,炎性病变患者36例。本研究显示,OPMDs与OSCC之间在S100A7染色(胞质和核)分布上存在统计学显著差异(P<0.05)。OSCC组、OPMD组和炎性病变组的核、胞质和膜染色以及染色强度具有显著不同的评分模式,OSCC组的S100A7染色评分最高(无论年龄)。
本研究得出结论,S100A7可作为一种诊断生物标志物,用于区分OPMDs和OSCC病变。然而,该标志物无法区分年轻和老年患者的OSCC,因为这两个年龄组肿瘤的分子发病机制可能相似。