Telomerase activity and terminal restriction fragment (TRF) length were examined in hepatocellular carcinoma (HCC). Telomerase activity was assayed by telomeric repeat amplification protocol (TRAP) connected with an internal telomerase assay standard (ITAS). The incidence of strong telomerase activity (highly variable level compared with the activity of non-cancerous liver tissue) was 79% in well, 84% in moderately, and 100% in poorly differentiated HCC, while 0% in non-cancerous liver tissues.
View Article and Find Full Text PDFNihon Shokakibyo Gakkai Zasshi
January 1998
Length of terminal restriction fragments (TRFs) was examined in 34 samples from hepatocellular carcinoma (HCC) patients. TRF length alterations (reduction or elongation) were found in 18 of 34 (53%) HCC nodules (13 cases reduced, 5 cases elongated). The incidence of TRF alteration was significantly higher in HCC exceeding 3 cm in diameter, moderately- or poorly-differentiated in histology, or with microscopic aggressive lesions (P<0.
View Article and Find Full Text PDFPrecise diagnosis of well-differentiated hepatocellular carcinoma (HCC) is sometimes difficult to establish. Telomerase activity was examined by telomeric-repeat-amplification protocol (TRAP) in 37 HCC nodules smaller than 3 cm in diameter, including 24 fine-needle-aspiration biopsy specimens, 22 non-tumor chronic-liver-disease tissues (9 chronic hepatitis and 13 liver cirrhosis) and 3 normal liver tissues. Telomerase activity was assayed by serially diluted samples and quantitated by using an internal telomerase assay standard (ITAS).
View Article and Find Full Text PDFDespite the recent advances in diagnostic techniques of HCC, diagnosis of HCC is still difficult and ambiguous when HCC is small and of the well differentiated type. The results presented here demonstrated that strong telomerase activity was frequently detected in HCC irrespective of the stage or size of the nodules but neither in non-tumor diseased liver nor in normal liver. Telomerase activity determination can be a useful additional tool for the diagnosis of early well-differentiated HCC.
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