Literature DB >> 19773378

DeltaNp63 overexpression, alone and in combination with other biomarkers, predicts the development of oral cancer in patients with leukoplakia.

Pierre Saintigny1, Adel K El-Naggar, Vali Papadimitrakopoulou, Hening Ren, You-Hong Fan, Lei Feng, J Jack Lee, Edward S Kim, Waun Ki Hong, Scott M Lippman, Li Mao.   

Abstract

PURPOSE: The risk of malignant transformation of oral preneoplastic lesion (OPL) is difficult to assess. DeltaNp63 is an early oncoprotein associated with mucosal tumorigenesis. The purpose of this study was to assess DeltaNp63 expression in OPL and its role as a marker of oral cancer risk. EXPERIMENTAL
DESIGN: DeltaNp63 expression was determined using immunohistochemistry in 152 OPL patients included in a clinical trial comparing retinyl palmitate alone or plus beta-carotene with low-dose 13-cis-retinoic acid. The associations between DeltaNp63 expression as well as DeltaNp63 expression with other potential risk factors for oral cancer development were analyzed.
RESULTS: DeltaNp63 expression was positive in 41 (27%) patients, clusters of intraepithelial inflammatory cells (EIC) were noted in 37 (26%) patients, and podoplanin (previously reported) was positive in 56 (37%) patients. Significantly more patients whose lesions were DeltaNp63 positive or exhibited EIC developed oral cancers. In the multicovariate analysis including age, treatment, and histologic status as cofactors, positive DeltaNp63 expression was associated with an increased hazard ratio of 3.308 (95% confidence interval, 1.663-6.580; P = 0.0007). Patients whose lesions showed positive DeltaNp63, podoplanin, and EIC had the highest oral cancer risk with a hazard ratio of 4.372 (95% confidence interval, 1.912-9.992; P = 0.0005) and 61% oral cancer development rate at 5 years compared with 15% of other OPL patients (P < 0.0001).
CONCLUSION: DeltaNp63 overepression in OPL is associated with increased oral cancer risk. Together, DeltaNp63, podoplanin, and EIC may be used as biomarkers to identify OPL patients with substantially high oral cancer risk.

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Year:  2009        PMID: 19773378      PMCID: PMC2756317          DOI: 10.1158/1078-0432.CCR-09-0498

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  45 in total

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4.  Overexpression of podoplanin in oral cancer and its association with poor clinical outcome.

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Journal:  Cancer       Date:  2006-08-01       Impact factor: 6.860

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Review 6.  Interventions for treating oral leukoplakia.

Authors:  G Lodi; A Sardella; C Bez; F Demarosi; A Carrassi
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Review 10.  The potential role of podoplanin in tumour invasion.

Authors:  A Wicki; G Christofori
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Review 2.  The pivotal role of pathology in the management of lung cancer.

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3.  ΔNp63 versatilely regulates a Broad NF-κB gene program and promotes squamous epithelial proliferation, migration, and inflammation.

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5.  World Workshop on Oral Medicine VII: Prognostic biomarkers in oral leukoplakia: A systematic review of longitudinal studies.

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10.  New DNA methylation markers and global DNA hypomethylation are associated with oral cancer development.

Authors:  Jean-Philippe Foy; Curtis R Pickering; Vassiliki A Papadimitrakopoulou; Jaroslav Jelinek; Steven H Lin; William N William; Mitchell J Frederick; Jing Wang; Wenhua Lang; Lei Feng; Li Zhang; Edward S Kim; You H Fan; Waun K Hong; Adel K El-Naggar; J Jack Lee; Jeffrey N Myers; Jean-Pierre Issa; Scott M Lippman; Li Mao; Pierre Saintigny
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