Background. Telomerase is activated in most human cancers but is inactivate
in adult somatic tissues except for some proliferating cell lineages. The
maintenance of telomerase activity may be a critical step of cellular immor
talization and transformation.
Materials and methods. We analyzed the expression of human telomerase rever
se transcriptase (hTERT) using in situ hybridization and compared it to Ki-
67 immunoreactivity in 29 cases of papillary thyroid carcinoma (PTC) and 17
cases of benign thyroid disease.
Results. The hTERT messenger RNA (mRNA) was expressed in the cytoplasm of c
arcinoma cells with moderate (n = 10) to strong intensity (n = 10) in 69% (
20 of 29) PTC cases. Human TERT was found in only 29% (5 of 17) cases of be
nign thyroid disease. Human TERT gene expression was preferentially detecte
d in PTC (P = 0.021). The Ki-67 labeling index was observed in 16 cases of
PTC (16 of 29; 55.2%). This result was significantly different from that of
benign thyroid disease (P = 0.014). The Ki-67 labeling index related to th
e intensity of hTERT mRNA expression (r = 0.51; P = 0.005) and was inversel
y associated with the follicular variant of PTC (r = -0.413; P = 0.026). No
statistically significant difference was found between hTERT expression an
d histological subtype of PTC.
Conclusions. Our results demonstrated that expression of hTERT could be det
ected using in situ hybridization in PTCs and was significantly distinguish
able from that of benign thyroid disease. Human TERT expression was related
to the Ki-67 labeling index, indicating that coupling of telomerase activa
tion with cell proliferation was the associated mechanism for tumorigenesis
. (C) 2001 Academic Press.