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Telomerase is a ribonucleoprotein enzyme responsible for the protection of telomeres - structures which play a key role in stabilizing chromosomes. Its presence assures the possibility of tissue regeneration and unlimited cell division. On the physiological level telomerase activity is present in germline cells, embryonic tissues and some hematopoetic stem cells and, on a pathological level, in neoplastic cells. Its expression causes uncontrolled cell proliferation and may be a characteristic marker of neoplastic transformation and tumor progression. The aim of the study was to present the presence of telomerase in neoplastic lymphocytes in cases of lymphoma malignum in dogs. Cytoimmunological procedure with Telomerase (catalytic unit) NCL-L-hTERT (Novocastra Ltd product) was used to locate telomerase in malignantly transformed lymphocytes and in normal lymphocytes. The study indicated that telomerase is not present in normal lymphocytes. Higher levels of telomerase were observed in cenroblastic and immunoblastic lymphoma cells, compared with lower amounts of the enzyme in lymphoma malignum lymphocyticum B cells. A distinct presence of the enzyme was also noted in lymphoma cells of skin T-receptors. The level of this ribonucleoprotein may serve as a malignancy marker of transformed lymphocytes.
The aim of this study was to discern whether telomerase activity might serve as a marker for canine skin tumors. Telomerase activity was measured in 57 samples of tumor tissues from operated dogs. Telomerase activity in the samples was measured using the diagnostic kit Telo TAGGG Telomerase PCR ELISA plus of ROCHE - photometric enzyme immunoassay for quantitative determination of telomerase activity, utilizing the telomeric repeat amplification protocol (TRAP). The samples were also investigated histopathologically. The performed investigations permitted the following conclusions: telomerase activity is substantially higher in malignant lesions then in benign lesions, but there is no differences between telomerase activity in benign lesions and normal skin. Telomerase activity in normal skin near malignant tumors is substantially higher then in normal skin from healthy dogs and there is no correlation between telomerase activity in malignant tumors and in the normal skin in their proximity.
The aim of the study was to evaluate the TRAP assay method of measuring telomerase activity in canine skin neoplasms. Telomerase activity was measured in 57 samples of tumor tissues from operated dogs. The samples were also subjected to histopathology investigations. Telomerase activity was measured using the Telo TAGGG Telomerase PCR ELISA diagnostic kit as well as ROCHE . photometric enzyme immunoassay for quantitative determination of telomerase activity, utilizing the telomere repeat amplification protocol (TRAP). The repetition, sensitivity and specificity of telomerase activity measurements were determined. TRAP assay performed in dogs has high repetition rate within high activity, and lower within small activity. This method is 100% sensitive and 34% specific.
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