Establishment and characterization of an oral squamous carcinoma cell line from a patient with no apparent habits associated with oral cancer

Sok, C.C. and Hamid, S. and Peng, L.K. and Ismail, S.M. and Zain, R.B. (2005) Establishment and characterization of an oral squamous carcinoma cell line from a patient with no apparent habits associated with oral cancer. Oral Oncology, 1 (1). p. 151. ISSN 1368-8375, DOI https://doi.org/10.1016/s1744-7895(05)80385-2.

[img] PDF
establishment.pdf
Restricted to Registered users only

Download (129kB) | Request a copy
[img]
Preview
PDF
Establishment_and_characterization_of_an_oral_squamous_carcinoma_cell_line_from_a_patient_with_no_apparent_habits_associated_with_oral_cancer.pdf

Download (28kB)
Official URL: https://doi.org/10.1016/s1744-7895(05)80385-2

Abstract

Introduction: We have established a cell line ORL-48(T) from a surgically resected specimen of an untreated primary human oral squamous cell carcinona of the mandible.This patient did not appear to have any oral habits which have been reported to be associated with oral cancer Materials and Method: The in vitro growth characteristics, epithelial origin, in vitro anchorage independency, HPV infection, microsatellite instability status, karyotype and the status of various cell cycle regulators and gatekeepers of the ORL-48(T) cell line were investigated. Results: The ORL-48(T) cell line is immortal, 3T3- independent and grew as a monolayer with the doubling time of 48h. Immunohistochemistry staining of cytokeratins confirmed the cell line is of epithelial origin. Soft agar assays demonstrated that ORL-48(T) expressed a low degree of anchorage independency (CFE<6). Karyotyping analysis revealed that ORL-48(T) is aneuploidy in which the number of chromosomes varied between 67 and 73. There is consistent trisomies of chromosomes 1, 2, 3, 5, 7, 9, 12, 15, 16 and 18 and homogenously staining region on 4q suggesting gene amplification in this region. Sequencing of exons 5, 6, 7, 9 and 10 of p53 revealed a mutation resulting in a stop codon. Molecular analysis of p14INK4a indicates hypermethylation of the p14INK4a promoter. In contrast to normal human keratinocytes, MDM2 is overpressed in ORL-48(T). Microsatellite analysis of BAT26 indicated that ORL-48(T) is microsatellite stable and this was confirmed by western blots demonstrating the expression of both hMSH2 and hMLH1 mismatch repair proteins. Polymerase chain reaction demonstrated that ORL-48(T) was not infected with human papillomavirus (HPV). Conclusion: This well characterized cell line will be useful tool in the understanding of the molecular changes associated with oral cancer particularly in cases where no clear aetiological factors are present.

Item Type: Article
Funders: UNSPECIFIED
Additional Information: Sok, CC Hamid, S Peng, LK Ismail, SM Zain, R 10th International Congress on Oral Cancer Apr 19-24, 2005 Crete, GREECE S
Uncontrolled Keywords: Oral squamous cell carcinoma, OSCC, lichenoid lesions, lichen planus, oral cancer, oral tumours, pemphigus, traumatic eosinophilic granuloma, aphthous ulcers, oral mucosal lesions, betel chewers mucosa, betel quid related lesions, betel quid, areca quid, tobacco quid, oral cancer screening, training and calibration, early detection, oral cancer awareness, biobanking, tissue bank, databank, oral cancer, tissue bank, research credibility, research ethics
Subjects: R Medicine > RK Dentistry > Oral surger
Divisions: Faculty of Dentistry > Dept of Oral Pathology & Oral Medicine & Periodontology
Depositing User: Prof. Dr. Rosnah Mohd Zain
Date Deposited: 09 Feb 2012 07:42
Last Modified: 13 Nov 2019 02:20
URI: http://eprints.um.edu.my/id/eprint/2570

Actions (login required)

View Item View Item