Literature DB >> 9070649

Amplification, increased dosage and in situ expression of the telomerase RNA gene in human cancer.

A I Soder1, S F Hoare, S Muir, J J Going, E K Parkinson, W N Keith.   

Abstract

Telomere length is maintained by the enzyme, telomerase, which has been linked to cellular immortality and tumour progression. However, the reasons for the high levels of telomerase found in human tumours are unknown. We have mapped the human telomerase RNA gene, (hTR), to chromosome 3q26.3 and show the hTR gene to be amplified in four carcinomas, (2/33 cervix, 1/31 head and neck, 1/9 lung). In addition, increased copy numbers of the hTR locus was also observed in 97% of tumours. By in situ hybridisation, the histological distribution of high levels of hTR expression could be demonstrated in a lung tumour and its metastasis with hTR amplification. These results are the first report of genetic alterations involving a known component of telomerase in human cancer. Indeed, it is also the first report of the amplification of a specific locus within the chromosome 3q region frequently subject to copy number gains in human tumours. In addition, we also show for the first time the histological distribution of the RNA component of telomerase in human tumours.

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Year:  1997        PMID: 9070649     DOI: 10.1038/sj.onc.1201066

Source DB:  PubMed          Journal:  Oncogene        ISSN: 0950-9232            Impact factor:   9.867


  35 in total

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4.  Mapping of the gene for the human telomerase reverse transcriptase, hTERT, to chromosome 5p15.33 by fluorescence in situ hybridization.

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Review 9.  DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies.

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10.  hTERT promoter activity and CpG methylation in HPV-induced carcinogenesis.

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