## Abstract Aberrant promoter hypermethylation of tumor‐associated genes leading to their inactivation is a common event in many cancer types. Using a sensitive restriction‐multiplex PCR method, we studied the promoter hypermethylation profile of the __p16, p15, hMLH1, MGMT__ and __E‐cad__ genes in
Tissue microarray evidence of association between p16 and phosphorylated eIF4E in tonsillar squamous cell carcinoma
✍ Scribed by Matthew G. Fury; Marija Drobnjak; Camelia S. Sima; Marina Asher; Jatin Shah; Nancy Lee; Diane Carlson; H. Guido Wendel; David G. Pfister
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 317 KB
- Volume
- 33
- Category
- Article
- ISSN
- 1043-3074
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✦ Synopsis
Abstract
Background.
Expression of p16 is a marker for human papillomavirus (HPV)‐related carcinogenesis in head and neck cancer. The purpose of this study is to determine if p16 immunoreactivity is associated with aberrant expression of components of the PI3 kinase pathway.
Methods.
A tissue microarray (TMA) was constructed for 46 archived tonsillar squamous cell carcinoma specimens. Clinical demographics of these patients were analyzed, and the TMA was interrogated with antibodies directed against p16, phosphorylated Akt^Ser473^, phosphorylated S6^Ser240/244^, phosphorylated S6^Ser235/236^, phosphorylated 4E‐BP1^Thr37/46^, phosphorylated eIF4E^Ser209^, PTEN, p21, and p53.
Results.
There was a significant correlation between history of tobacco abuse (>10 pack/years) and absence of p16 expression (p = .01). Expression of p16 was significantly associated with immunoreactivity of p21 (p = .02), PTEN (p = .02), and phosphorylated eIF4E (p = .03). There was no evidence of association between p16 status and expression of phosphorylated S6, phosphorylated 4E‐BP1, or p53.
Conclusion.
p16 positive tonsillar squamous cell carcinoma is characterized by expression of phosphorylated eIF4E that may occur via a mammalian target of rapamycin (mTOR)‐independent mechanism. © 2010 Wiley Periodicals, Inc. Head Neck, 2010
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## Abstract ## BACKGROUND: The tumor protein p73 interacts with the human papillomavirus type 16 (HPV‐16) oncoproteins E6 and E7, and __p73__ variation may modify the interaction between p73 protein and HPV‐16 oncogenic proteins and contribute to cellular malignant transformation. ## METHODS: In