학술논문

Gene expression in cell lines from human ameloblastoma immortalized using hTERT and HPV16‐E6/E7.
Document Type
Article
Source
Oral Diseases. Nov2022, Vol. 28 Issue 8, p2230-2238. 9p. 1 Black and White Photograph, 2 Diagrams, 2 Charts.
Subject
*PAPILLOMAVIRUSES
*AMELOBLASTOMA
*CELL culture
*NEOPLASTIC cell transformation
*GENE expression profiling
*TRANSFERASES
*MESSENGER RNA
*GENOMES
*CELL lines
*POLYMERASE chain reaction
Language
ISSN
1354-523X
Abstract
Objective: The aim of this study was to evaluate and compare alterations in gene expression using two distinct immortalization methods (hTERT and HPV16‐E6/E7) in ameloblastoma cell lines. Materials and Methods: A primary cell culture derived from human ameloblastoma (AME‐1) was established and immortalized by two different methods using a transfection processes to hTERT and HPV‐E6/E7. The RNA‐seq was used to verify which immortalization method had less influence on gene expression. It was performed in four steps: extraction and collection of mRNA, PCR amplification, comparison with the human reference genome, and analysis of differential expression. The genes with differentiated expression were identified and mapped. Results: RNA‐seq revealed genetic alterations in ameloblastoma cell lines after the immortalization process, including increased expression of tumor genes like MYC, E2F1, BRAF, HRAS, and HTERT, and a decrease in tumor suppressor genes like P53, P21, and Rb. Conclusions: It is possible to affirm that cell immortalization is not an inert method regarding gene regulation mechanisms and the hTERT method (AME‐TERT) presented fewer changes in gene expression levels. [ABSTRACT FROM AUTHOR]