The ectopic expression of telomerase(1-2) in normal human cells results in
an extended lifespan(3-4), indicating that telomere shortening regulates th
e timing of cellular senescence, As telomerase expression is a hallmark of
cancer, we investigated the long-term effects of forced expression of human
telomerase catalytic component (hTERT) in normal human fibroblasts. In vit
ro growth requirements, cell-cycle checkpoints and karyotypic stability in
telomerase-expressing cells are similar to those of untransfected controls.
In addition, co-expression of telomerase, the viral oncoproteins HPV16 E6/
E7 (which inactivate p53 and pRB) and oncogenic HRAS does not result in gro
wth in soft agar, Thus, although ectopic expression of telomerase in human
fibroblasts is sufficient for immortalization, it does not result in change
s typically associated with malignant transformation.