Targeting of chemoprevention to high-risk potentially malignant oral lesions: Challenges and opportunities

Victor D. Martinez, Calum E. MacAulay, Martial Guillaud, Wan L. Lam, Lewei Zhang, Kitty K. Corbett, Miriam P. Rosin

Résultat de recherche: Articleexamen par les pairs

7 Citations (Scopus)

Résumé

Worldwide, oral cancer is responsible for 170,000 deaths per year. Intervention to prevent this disease is a long sought after goal. Chemoprevention studies have focused on clinicopathological features of potentially malignant lesions (PML) in an effort to prevent their progression to cancer. However, prediction of future behavior for such lesions is difficult and remains a major challenge to such intervention. Different approaches to this problem have been tested in the past 20 years. Early genetic progression models identified critical regions of allelic imbalance at 3p and 9p, and provided the basis for molecular markers to identify progressing PMLs. Subsequently, technological advances, such as genome-wide high-throughput array platforms, computer imaging, visualization technology and next generation sequencing, have broadened the scope for marker development and have the potential of further improving our ability to identify high-risk lesions in the near future either alone or in combination. In this article, we examine the milestones in the development of markers for PML progression. We emphasize the critical importance of networks among scientists, health professionals and community to facilitate the validation and application of putative markers into clinical practice. With a growing number of new agents to validate, it is necessary to coordinate the design and implementation of strategies for patient recruitment, integration of marker assessment, and the final translation of such approaches into clinical use.

Langue d'origineEnglish
Pages (de-à)1123-1130
Nombre de pages8
JournalOral Oncology
Volume50
Numéro de publication12
DOI
Statut de publicationPublished - déc. 1 2014
Publié à l'externeOui

Note bibliographique

Funding Information:
This work was supported by grants from the NIH and the National Institute of Dental and Craniofacial Research ( R01DE13124 , R01DE17013 and R01 DE015965 ).

Publisher Copyright:
© 2014 Elsevier Ltd.

ASJC Scopus Subject Areas

  • Oral Surgery
  • Oncology
  • Cancer Research

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural

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