Literature DB >> 34376461

Predicting Progression of Low-Grade Oral Dysplasia Using Brushing-Based DNA Ploidy and Chromatin Organization Analysis.

Madhurima Datta1,2,3, Denise M Laronde1,2, Miriam P Rosin2,4, Lewei Zhang1,2,5, Bertrand Chan1,2, Martial Guillaud6,7.   

Abstract

Most oral cancers arise from oral potentially malignant lesions, which show varying grades of dysplasia. Risk of progression increases with increasing grade of dysplasia; however, risk prediction among oral low-grade dysplasia (LGD), that is, mild and moderate dysplasia can be challenging as only 5%-15% transform. Moreover, grading of dysplasia is subjective and varies with the area of the lesion being biopsied. To date, no biomarkers or tools are used clinically to triage oral LGDs. This study uses a combination of DNA ploidy and chromatin organization (CO) scores from cells obtained from lesion brushings to identify oral LGDs at high-risk of progression. A total of 130 lesion brushings from patients with oral LGDs were selected of which 16 (12.3%) lesions progressed to severe dysplasia or cancer. DNA ploidy and CO scores were analyzed from nuclear features measured by our in-house DNA image cytometry (DNA-ICM) system and used to classify brushings into low-risk and high-risk. A total of 57 samples were classified as high-risk of which 13 were progressors. High-risk DNA brushing was significant for progression (P = 0.001) and grade of dysplasia (P = 0.004). Multivariate analysis showed high-risk DNA brushing showed 5.1- to 8-fold increased risk of progression, a stronger predictor than dysplasia grading and lesion clinical features. DNA-ICM can serve as a non-invasive, high-throughput tool to identify high-risk lesions several years before transformation. This will help clinicians focus on such lesions whereas low-risk lesions may be spared from unnecessary biopsies.Prevention Relevance: DNA ploidy and chromatin organization of cells collected from oral potentially malignant lesions (OPMLs) can identify lesions at high-risk of progression several years prior. This non-invasive test would enable clinicians to triage high-risk (OPMLs) for closer follow-up while low-risk lesions can undergo less frequent biopsies reducing burden on healthcare resources. ©2021 American Association for Cancer Research.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 34376461      PMCID: PMC8639617          DOI: 10.1158/1940-6207.CAPR-21-0134

Source DB:  PubMed          Journal:  Cancer Prev Res (Phila)        ISSN: 1940-6215


  43 in total

Review 1.  Clinical application of DNA ploidy to cervical cancer screening: A review.

Authors:  David Garner
Journal:  World J Clin Oncol       Date:  2014-12-10

Review 2.  Oral leukoplakia-to treat or not to treat.

Authors:  P Holmstrup; E Dabelsteen
Journal:  Oral Dis       Date:  2016-02-11       Impact factor: 3.511

3.  Dysplasia Should Not Be Ignored in Lichenoid Mucositis.

Authors:  L D Rock; D M Laronde; I Lin; M P Rosin; B Chan; B Shariati; L Zhang
Journal:  J Dent Res       Date:  2018-01-12       Impact factor: 6.116

4.  Chromosome instability predicts the progression of premalignant oral lesions.

Authors:  T J H Siebers; V E Bergshoeff; I Otte-Höller; B Kremer; E J M Speel; J A W M van der Laak; M A W Merkx; P J Slootweg
Journal:  Oral Oncol       Date:  2013-09-26       Impact factor: 5.337

5.  Oral dysplasia: biomarkers, treatment, and follow-up.

Authors:  Paul Nankivell; Hisham Mehanna
Journal:  Curr Oncol Rep       Date:  2011-04       Impact factor: 5.075

6.  Potential use of quantitative tissue phenotype to predict malignant risk for oral premalignant lesions.

Authors:  Martial Guillaud; Lewei Zhang; Catherine Poh; Miriam P Rosin; Calum MacAulay
Journal:  Cancer Res       Date:  2008-05-01       Impact factor: 12.701

7.  Biopsy and histopathologic diagnosis of oral premalignant and malignant lesions.

Authors:  Catherine F Poh; Samson Ng; Kenneth W Berean; P Michele Williams; Miriam P Rosin; Lewei Zhang
Journal:  J Can Dent Assoc       Date:  2008-04       Impact factor: 1.316

8.  Abnormal DNA content in oral epithelial dysplasia is associated with increased risk of progression to carcinoma.

Authors:  G Bradley; E W Odell; S Raphael; J Ho; L W Le; S Benchimol; S Kamel-Reid
Journal:  Br J Cancer       Date:  2010-09-21       Impact factor: 7.640

9.  Oral Leukoplakia and Risk of Progression to Oral Cancer: A Population-Based Cohort Study.

Authors:  Anil K Chaturvedi; Natalia Udaltsova; Eric A Engels; Jed A Katzel; Elizabeth L Yanik; Hormuzd A Katki; Mark W Lingen; Michael J Silverberg
Journal:  J Natl Cancer Inst       Date:  2020-10-01       Impact factor: 13.506

10.  Oral epithelial dysplasia classification systems: predictive value, utility, weaknesses and scope for improvement.

Authors:  S Warnakulasuriya; J Reibel; J Bouquot; E Dabelsteen
Journal:  J Oral Pathol Med       Date:  2008-03       Impact factor: 4.253

View more
  2 in total

1.  Relationship of DNA aneuploidy with distinctive features of oral potentially malignant disorders: A cytological analysis of 748 cases.

Authors:  Yanyi Tang; Lijun Liu; Chenxi Li; Wei Liu; Linjun Shi
Journal:  J Dent Sci       Date:  2021-10-26       Impact factor: 3.719

Review 2.  Alcohol and Head and Neck Cancer: Updates on the Role of Oxidative Stress, Genetic, Epigenetics, Oral Microbiota, Antioxidants, and Alkylating Agents.

Authors:  Giampiero Ferraguti; Sergio Terracina; Carla Petrella; Antonio Greco; Antonio Minni; Marco Lucarelli; Enzo Agostinelli; Massimo Ralli; Marco de Vincentiis; Giammarco Raponi; Antonella Polimeni; Mauro Ceccanti; Brunella Caronti; Maria Grazia Di Certo; Christian Barbato; Alessandro Mattia; Luigi Tarani; Marco Fiore
Journal:  Antioxidants (Basel)       Date:  2022-01-11
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.