The extremities of chromosomes, Or telomeres, play a critical role in the c
ontrol cell proliferation. Changes in their structure can induce either an
arrest of cell division (replicative senescence) or cell death (apoptosis).
Those "telomeric barriers against proliferation" can stop the development
of tumor cells. Some recent results obtained with mice lacking a functional
telomerase enzyme and in successive generations of mice doubly inactivated
for telomerase and the INK4a or the p53 tumor suppressor genes are particu
larly relevant to oncogenesis. It appears that manipulating telomeres becom
es a challenge for the design of future anti-oncogenic approaches.