Abstract

The enzyme telomerase reverse transcriptase (TERT) is essential for telomere maintenance. In replicating cells, maintenance of telomere length is important for the preservation of vital genetic information and prevention of genomic instability. A common genetic variant in TERT, rs2736100 C/A, is associated with both telomere length and multiple diseases. Carriage of the C allele is associated with longer telomere length, while carriage of the A allele is associated with shorter telomere length. Furthermore, some diseases have a positive association with the C and some with the A allele. In this study, meta-analyses were performed for two groups of diseases, cancerous diseases, e.g., lung cancer and non-cancerous diseases, e.g., pulmonary fibrosis, using data from genome-wide association studies and case-control studies. In the meta-analysis it was found that cancer positively associated with the C allele (pooled OR 1.16 [95% CI 1.09–1.23]) and non-cancerous diseases negatively associated with the C allele (pooled OR 0.81 [95% CI 0.65–0.99]). This observation illustrates that the ambiguous role of telomere maintenance in disease hinges, at least in part, on a single locus in telomerase genes. The dual role of this single nucleotide polymorphism also emphasizes that therapeutic agents aimed at influencing telomere maintenance should be used with caution.

Highlights

  • Telomere biology is emerging as a significant factor in an increasing number of diseases [1,2,3,4]

  • A meta-analysis was performed to analyze the association of telomerase reverse transcriptase (TERT) single nucleotide polymorphism (SNP) rs2736100 with a group of cancer diseases and with a group of non-cancerous diseases

  • For the non-cancer group, 8 studies were found with diagnoses of pulmonary fibrosis and coronary heart disease among others

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Summary

Introduction

Telomere biology is emerging as a significant factor in an increasing number of diseases [1,2,3,4]. Studies have found disease associations with both abnormal telomere length and with genetic variants are related to telomere biology [5,6,7]. Telomeres are non-coding tandem repeats spatially organized by specialized proteins that maintain stability of the chromosome ends [8,9,10]. Telomeres serve as a buffer against the shortening of chromosomes, thereby preventing the loss of vital genetic information [11]. Telomeres can be elongated by the ribonucleoprotein telomerase [12, 13]. Telomerase consists of a catalytic protein component, encoded by the gene telomerase reverse transcriptase (TERT), and a RNA template, encoded by telomerase RNA component

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