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Can dual staining with p16 and Ki67 be biomarkers of epithelial dysplasia in oral lesions?
Bharti, Anju; Qayoom, Sumaira; Jaiswal, Riddhi; Agarwal, Preeti; Singh, R K; Agarwal, S P; Bhalla, Shalini; Makker, Annu; Goel, Madhu Mati.
Afiliação
  • Bharti A; Department of Pathology, Institute of Medical Sciences, BHU, Varanasi, Uttar Pradesh, India.
  • Qayoom S; Department of Pathology, KGMU, Lucknow, Uttar Pradesh, India.
  • Jaiswal R; Department of Pathology, KGMU, Lucknow, Uttar Pradesh, India.
  • Agarwal P; Department of Pathology, KGMU, Lucknow, Uttar Pradesh, India.
  • Singh RK; Department of Maxillofacial Surgery & Otorhinolaryngology, KGMU, Lucknow, Uttar Pradesh, India.
  • Agarwal SP; Department of Maxillofacial Surgery & Otorhinolaryngology, KGMU, Lucknow, Uttar Pradesh, India.
  • Bhalla S; Department of Pathology, KGMU, Lucknow, Uttar Pradesh, India.
  • Makker A; Department of Biochemistry, Prasad Institute of Medical Sciences, Lucknow, Uttar Pradesh, India.
  • Goel MM; Department of Pathology, KGMU, Lucknow, Uttar Pradesh, India.
J Cancer Res Ther ; 18(4): 1003-1008, 2022.
Article em En | MEDLINE | ID: mdl-36149153
ABSTRACT

Background:

Oral carcinogenesis is a multistage process with epithelial dysplasia as a premalignant condition. There is a significant inter-observer variation in diagnosing and grading the oral epithelial dysplasia. As human papillomavirus (HPV) is believed to have à strong relationship with oral carcinogenesis, using P16 as a biomarker may help in identifying the cells which may be undergoing the malignant transformation. However, due to the low specificity of P16, dual staining test P16INK4/Ki67 might be a better promising marker for identifying the transformed cells. This study was designed to evaluate the dual expression of P16 and Ki67 as a promising biomarker for dysplasia and their correlation with clinicopathological factors. Materials and

Methods:

Immunohistochemical analysis for p16 and ki67 was performed on 30 premalignant oral lesions and 36 oral squamous cell carcinoma (OSCC) by dual staining using the CINtec PLUS kit.

Results:

CINtec positivity was observed only in leukoplakia with dysplasia (46.7%) and squamous cell carcinoma (25%). None of the cases of leukoplakia without dysplasia or oral submucosal fibrosis stained positive for CINtec plus staining. In leukoplakia with dysplasia, there was no significant association with any of the clinicopathological parameters studied. In OSCC cases, alcohol intake showed statistically significant association with CINtec positivity.

Conclusion:

P16INK4/Ki67 assessment by dual staining is a promising biomarker for identifying dysplasia in cases with diagnostic dilemmas.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Neoplasias Bucais / Carcinoma de Células Escamosas / Infecções por Papillomavirus Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cancer Res Ther Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Neoplasias Bucais / Carcinoma de Células Escamosas / Infecções por Papillomavirus Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: J Cancer Res Ther Ano de publicação: 2022 Tipo de documento: Article