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RNAscope for In situ Detection of Transcriptionally Active Human Papillomavirus in Head and Neck Squamous Cell Carcinoma
Published on: March 11, 2014
Overexpression of p68 mRNA in head and neck squamous cell carcinoma cells
Ulf Henning Beier1, Steffen Maune, Jens E Meyer
1Department of Pediatrics, University of Illinois at Chicago, 840 South Wood St., Room 1438 CSB, Chicago, Illinois 60612-7324, USA.
Background:
Head and neck squamous cell carcinomas (HNSCC) are aggressively growing tumors with only marginal improvement in outcome despite ongoing developments in treatment protocols. This problem has been associated with a lack of therapy individualization on tumor biological properties.
Materials And Methods:
mRNA expression profiles of HNSCC and normal epithelial cells were compared in order to identify genes associated with cancer formation. Differential display was used to trace gene fragments showing differential expression in HNSCC cells, which were than isolated, re-amplified, cloned and sequenced.
Results:
A 131-bp-long fragment was identified to be overexpressed in HNSCC cells that revealed a 99.3% homology with p68 mRNA. The differential expression was confirmed by Northern hybridization.
Conclusion:
The data presented suggest an involvement of p68 in the process of malignant transformation or progression of HNSCC.
Insights
Overexpression of p68 mRNA in head and neck squamous cell carcinomas (HNSCC) suggests its role in cancer development. This finding may lead to more personalized HNSCC therapies based on tumor biology.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Head and neck squamous cell carcinomas (HNSCC) exhibit aggressive growth with limited treatment outcome improvements.
- Lack of therapy individualization based on tumor biology contributes to poor outcomes in HNSCC.
Purpose of the Study:
- To identify genes associated with HNSCC formation by comparing mRNA expression profiles.
- To investigate the role of specific gene fragments in the malignant transformation of HNSCC.
Main Methods:
- Differential display technique to identify differentially expressed gene fragments in HNSCC.
- Isolation, re-amplification, cloning, and sequencing of identified gene fragments.
- Confirmation of differential gene expression using Northern hybridization.
Main Results:
- A 131-bp fragment overexpressed in HNSCC cells was identified.
- The fragment showed 99.3% homology to p68 mRNA.
- Differential expression of p68 was confirmed in HNSCC.
Conclusions:
- The findings suggest p68 mRNA is involved in the malignant transformation or progression of HNSCC.
- p68 may serve as a potential biomarker or therapeutic target for HNSCC.
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