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起源于口腔黏膜下纤维化且伴有p16INK4A阳性和细胞衰老的人乳头瘤病毒阴性口腔鳞状细胞癌:一例报告

HPV-Negative Oral Squamous Cell Carcinoma Arising from Oral Submucous Fibrosis with p16INK4A Positivity and Cellular Senescence: A Case Report.

作者信息

Chaurasia Akhilanand, Pantelis Pavlos, Theocharous Giorgos, Veroutis Dimitris, Kotsinas Athanassios, Gorgouli Eva V, Georgakopoulou Eleni

机构信息

Department of Oral Medicine and Radiology, King George Medical University, India.

Molecular Carcinogenesis Group, Department of Histology and Embryology, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

J Clin Exp Dent. 2025 Apr 1;17(4):e479-e482. doi: 10.4317/jced.62698. eCollection 2025 Apr.

Abstract

BACKGROUND

Oral Submucous Fibrosis (OSF) is a chronic, progressive, and potentially malignant disorder primarily associated with areca nut chewing. While Oral Squamous Cell Carcinoma (OSCC) typically develops in the tongue and floor of the mouth, its occurrence in the buccal mucosa in the context of OSF is less common. The molecular mechanisms underlying OSF-associated OSCC remain unclear. p16INK4A is widely recognized as a surrogate marker for HPV-driven carcinogenesis; however, its role as an indicator of cellular senescence is increasingly acknowledged. Given that senescence contributes to various pathologies, including cancer, this case report explores its potential role in the pathogenesis of OSF-associated OSCC.

CASE PRESENTATION

We present the case of a 39-year-old male with a 10-year history of gutkha chewing, who developed clinically advanced OSF and a well-differentiated OSCC of the buccal mucosa. Immunohistochemical (IHC) analysis revealed strong p16INK4A expression, increased p21WAF1/cip1 levels, and low Ki67 proliferative activity. Notably, Polymerase Chain Reaction (PCR) testing for HPV was negative. Further staining with SenTraGor (GL13) confirmed the presence of senescent cells, suggesting that p16INK4A overexpression in this case reflects cellular senescence rather than an HPV-driven oncogenic process.

CONCLUSIONS

This case highlights the necessity of thorough molecular assessment when interpreting p16INK4A positivity in OSF-associated OSCC. The HPV-negative status, coupled with senescence markers, suggests that p16INK4A expression in such cases may show a senescence-associated tumorigenic pathway rather than HPV-mediated carcinogenesis. These findings support the inclusion of cellular senescence markers like SenTraGor in the diagnostic evaluation of OSCC arising from OSF. Oral Submucous Fibrosis, OSCC, p16INK4A, Cellular Senescence, HPV-Negative, Buccal Mucosa, SenTraGor.

摘要

背景

口腔黏膜下纤维化(OSF)是一种慢性、进行性且具有潜在恶性的疾病,主要与嚼槟榔有关。虽然口腔鳞状细胞癌(OSCC)通常发生于舌部和口底,但在OSF背景下发生于颊黏膜的情况较少见。OSF相关OSCC的分子机制尚不清楚。p16INK4A被广泛认为是HPV驱动致癌作用的替代标志物;然而,其作为细胞衰老指标的作用也日益受到认可。鉴于衰老与包括癌症在内的多种病理过程有关,本病例报告探讨了其在OSF相关OSCC发病机制中的潜在作用。

病例介绍

我们报告一例39岁男性,有10年嚼烟草史,出现临床晚期OSF及颊黏膜高分化OSCC。免疫组织化学(IHC)分析显示p16INK4A强表达、p21WAF1/cip1水平升高及Ki67增殖活性低。值得注意的是,HPV聚合酶链反应(PCR)检测为阴性。用SenTraGor(GL13)进一步染色证实存在衰老细胞,表明该病例中p16INK4A过表达反映细胞衰老而非HPV驱动的致癌过程。

结论

本病例强调在解释OSF相关OSCC中p16INK4A阳性时进行全面分子评估的必要性。HPV阴性状态及衰老标志物表明,此类病例中p16INK4A表达可能显示与衰老相关的致瘤途径而非HPV介导的致癌作用。这些发现支持将SenTraGor等细胞衰老标志物纳入OSF相关OSCC的诊断评估中。口腔黏膜下纤维化、OSCC、p16INK4A、细胞衰老、HPV阴性、颊黏膜、SenTraGor。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85c/12077832/37db3439dd9b/jced-17-e479-g001.jpg

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