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(The FASEB Journal. 1998;12:801-811.)
© 1998 FASEB


RESEARCH COMMUNICATION

Antisense telomerase treatment: induction of two distinct pathways, apoptosis and differentiation

Seiji Kondoa,1, Yoshikazu Tanakad, Yasuko Kondob, Masahiro Hitomic, Gene H. Barnetta, Yukihito Ishizakae, Jinbo Liua, Talat Haqqia, Akiko Nishiyamab, Bryant Villeponteauf, John K. Cowella,b, and Barbara P. Barnaa

a Department of Neurosurgery, Brain Tumor/Neuro-Oncology Center, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA
b Department of Neurosciences, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA
c Department of Molecular Biology, The Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA
d Department of Microbiology, The Tokyo Metropolitan Institute of Medical Science, Tokyo 113, Japan
e Department of Hematology, Research Institute, International Medical Center of Japan, Tokyo 162, Japan
f Geron Corporation, 200 Constitution Drive, Menlo Park, California 94025, USA

Telomerase, the enzyme that elongates telomeric DNA (TTAGGG)n, may be involved in cellular immortality and oncogenesis. To investigate the effect of inhibition of telomerase on tumor cells, we transfected the antisense vector against the human telomerase RNA into human malignant glioma cells exhibiting telomerase activity. After 30 doublings, some subpopulations of transfectants expressed a high level of interleukin-1ß-converting enzyme (ICE)2 protein and underwent apoptosis. In contrast, other subpopulations also showed enhanced ICE protein but escaped from apoptotic crisis and continued to grow, although their DNA synthesis, invasive ability, and tumorigenicity in nude mice were significantly reduced. Surviving cells demonstrated increased expression of glial fibrillary acidic protein and decreased motility, consistent with a more differentiated state. These cells also contained enhanced expression of the cyclin-dependent kinase inhibitors (CDKIs) p21 and p27. Treatment of surviving nonapoptotic cells with antisense oligonucleotides against p27, but not p21, induced apoptotic cell death, suggesting that p27 may have protected differentiating glioma cells from apoptosis. These data show that treatment with antisense telomerase inhibits telomerase activity and subsequently induces either apoptosis or differentiation. Regulation of these two distinct pathways may be dependent on the expression of ICE or CDKIs.—Kondo, S., Tanaka, Y., Kondo, Y., Hitomi, M., Barnett, G. H., Ishizaka, Y., Liu, J., Haqqi, T., Nishiyama, A., Villeponteau, B., Cowell, J. K., Barna, B. P. Antisense telomerase treatment: induction of two distinct pathways, apoptosis and differentiation FASEB J. 12, 801–811 (1998)


Key Words: ICE • p27 • CDKI • tumor cells • tumorigenicity • oglionucleotide




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