Afkhami Michelle, Maghami Ellie, Gernon Thomas J, Villaflor Victoria, Bell Diana
Molecular Pathology and Therapy Biomarkers, Division of Laboratory Medicine, City of Hope Cancer Center, 1500 Duarte Rd., CA 91010, United States of America.
Head and Neck Surgery, Division of Surgery, City of Hope Cancer Center, 1500 Duarte Rd., CA 91010, United States of America.
Ann Diagn Pathol. 2023 Apr;63:152104. doi: 10.1016/j.anndiagpath.2023.152104. Epub 2023 Jan 6.
Oral proliferative verrucous leukoplakia (OPVL) is a chronic form of oral leukoplakia that progresses to a multifocal disease with confluent, exophytic and proliferative features. The clinical differential diagnosis for OPVL includes frictional keratosis, leukoplakia, chronic hyperplastic candidiasis, squamous papilloma, verrucous hyperplasia, verrucous carcinoma and squamous cell carcinoma. In this study, we aimed to delineate the dynamic changes in molecular signature during OPVL progression. We compare to a cohort of oral cavity keratinizing squamous cell carcinoma (OSCC) patients covering the spectrum of verrucous carcinoma to invasive squamous cell carcinoma including cytologically bland cuniculatum variant.
Samples from a large OPVL lesion that exhibited a histopathologic continuum of OPVL progression.
Canonical hotspot TERT promoter mutations were identified in all patients. TERT C228T was dominant and mutually exclusive with TERT C250T. In patients with TERT C250T, there was concurrent PI3 point mutation. TP53 mutations were also consistently found (8/10). At the protein level, p53 was abnormal, with loss of function and gain of function.
OPVL is a pathology that shows proximity to the gene expression profile of OSCC, highlighting signatures in common that can be important targets for drug treatment, as well as in the development of diagnostic and prognostic strategies for this disease.
口腔增殖性疣状白斑(OPVL)是一种慢性口腔白斑,会发展为具有融合性、外生性和增殖性特征的多灶性疾病。OPVL的临床鉴别诊断包括摩擦性角化病、白斑、慢性增生性念珠菌病、鳞状乳头瘤、疣状增生、疣状癌和鳞状细胞癌。在本研究中,我们旨在描绘OPVL进展过程中分子特征的动态变化。我们将其与一组口腔角化性鳞状细胞癌(OSCC)患者进行比较,这些患者涵盖了从疣状癌到浸润性鳞状细胞癌的范围,包括细胞学上温和的隧道状亚型。
从一个呈现OPVL进展组织病理学连续变化的大型OPVL病变中获取样本。
在所有患者中均鉴定出典型的热点TERT启动子突变。TERT C228T占主导地位,且与TERT C250T相互排斥。在携带TERT C250T的患者中,同时存在PI3点突变。还一致发现了TP53突变(8/10)。在蛋白质水平上,p53异常,存在功能丧失和功能获得。
OPVL是一种在基因表达谱上与OSCC相近的病理学疾病,突出了共同的特征,这些特征可能是药物治疗的重要靶点,以及该疾病诊断和预后策略制定中的重要靶点。