Gene mutations and increased levels of p53 protein in human squamous cell carcinomas and their cell lines

• Published in: British journal of cancer 1993-06, Vol.67 (6), p.1274-1284
• Main Authors: Burns, JE, Baird, MC, Clark, LJ, Burns, PA, Edington, K, Chapman, C, Mitchell, R, Robertson, G, Soutar, D, Parkinson, EK
• Format: Article
• Language: English
• Subjects: Base Sequence; Biological and medical sciences; Biomedical and Life Sciences; Biomedicine; Cancer Research; Carcinoma, Squamous Cell - genetics; Carcinoma, Squamous Cell - metabolism; Carcinoma, Squamous Cell - microbiology; Dermatology; DNA, Viral - analysis; DNA, Viral - genetics; Drug Resistance; Epidemiology; experimental-therapeutics; Genes, p53 - genetics; Head and Neck Neoplasms - genetics; Head and Neck Neoplasms - metabolism; Head and Neck Neoplasms - microbiology; Humans; Immunohistochemistry; Keratinocytes - metabolism; Keratinocytes - physiology; Medical sciences; Molecular Medicine; Molecular Sequence Data; Mouth - metabolism; Mouth - physiology; Mouth Neoplasms - genetics; Mouth Neoplasms - metabolism; Mouth Neoplasms - microbiology; Mutation; Oncology; Papillomaviridae - genetics; Tumor Suppressor Protein p53 - genetics; Tumor Suppressor Protein p53 - metabolism; Tumors of the skin and soft tissue. Premalignant lesions
• ISSN: 0007-0920; 1532-1827
• DOI: 10.1038/bjc.1993.238

Using immunocytochemical and Western blotting techniques we have demonstrated the presence of abnormally high levels of p53 protein in 8/24 (33%) of human squamous cell carcinomas (SCC) and 9/18 (50%) of SCC cell lines. There was a correlation between the immunocytochemical results obtained with eight SCC samples and their corresponding cell lines. Direct sequencing of PCR-amplified, reverse transcribed, p53 mRNA confirmed the expression of point mutations in six of the positive cell lines and detected in-frame deletions in two others. We also detected two stop mutations and three out-of-frame deletions in five lines which did not express elevated levels of p53 protein. Several of the mutations found in SCC of the tongue (3/7) were in a region (codons 144-166) previously identified as being a p53 mutational hot spot in non-small cell lung tumours (Mitsudomi et al., 1992). In 11/13 cases only the mutant alleles were expressed suggesting loss or reduced expression of the wild type alleles in these cases. Six of the mutations were also detected in the SCCs from which the lines were derived, strongly suggesting that the mutations occurred, and were selected, in vivo. The 12th mutation GTG-->GGG (valine-->glycine) at codon 216 was expressed in line SCC-12 clone B along with an apparently normal p53 allele and is to our knowledge a novel mutation. Line BICR-19 also expressed a normal p53 allele in addition to one where exon 10 was deleted. Additionally 15 of the SCC lines (including all of those which did not show elevated p53 protein levels) were screened for the presence of human papillomavirus types 16 and 18 and were found to be negative. These results are discussed in relation to the pathogenesis of SCC and the immortalisation of human keratinocytes in vitro.