Telomerase is attracting great interest as a target for anticancer research
because telomerase activity is present in most malignant cells, but undete
ctable in most normal somatic cells. The antisense approach has been widely
exploited and directed to telomerase RNA, chiefly the template region. Rib
ozymes have been less investigated. Agents that stabilize folded G-quadrupl
ex structures also inhibit telomerase. Inhibitory agents from many chemical
classes have been identified many through screening, but their specificity
of action is in doubt. A specific inhibitor is expected to immediately inh
ibit activity but not cell division, produce telomerase shortening over mul
tiple generations, and ultimately produce end-to-end chromosomal fusion and
growth arrest.