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Telomerase is the enzyme that replenishes shortened telomeres and allows
cells to reproduce indefinitely. Found in only a few normal human cells,
telomerase is present in as many as 90% of human cancers. This makes telomerase
an attractive candidate for highly selective cancer drugs.12
The evidence that activation of telomerase is necessary for most cancers
to thrive is strong.13 Indeed, some scientists believe that
telomerase activation is the main pathway by which cancer cells become
immortal, that is, able to reproduce forever without limits. Certain normal
human cells can only undergo 30-50 doublings before their telomeres are
too short and doubling stops. Cancer cells must undergo about 80 doublings
before a tumor mass is large enough to be detected. Thus, say researchers,
telomerase activation is necessary for cancers to grow.14
Detection of telomerase activity could potentially be used as a marker
for cancer, a blood, fluid or tissue test that doctors could use to determine
whether cancer is present or has recurred after treatment.15
Indeed, telomerase activity has been found to be a marker for one type
of deadly cancer already. Early neuroblastomas, tumors of the central
nervous system, have little or no detectable telomerase activity, and
they generally have a favorable prognosis. Late stage neuroblastomas have
high telomerase activity and typically have a grim prognosis.16
A number of researchers have suggested that if telomerase is required
for so many cancers to flourish, perhaps anti-telomerase drugs could be
developed as cancer-fighting agents. Some have suggested that such a drug
would have minimal side effects, since so few normal cells have active
telomerase.17 Others caution that some side effects are possible.
Those potential side effects include:
Blood toxicity:
Some populations of stem cells, which are the parents of mature blood
cells, do use telomerase. Anti-telomerase drugs could, therefore, suppress
the production of vital blood cells.
Immune toxicity:
Some infection-fighting cells use telomerase normally. Anti-telomerase
drugs, therefore, could theoretically weaken our ability to fight infection.
Skin toxicity:
While most of our skin cells have little telomerase activity, those that
repair wounds do have some. Anti-telomerase drugs might cause delayed
wound healing.
Gonadal toxicity:
Some normal telomerase activity is seen in the cells of the ovary and
testis. Thus, anti-telomerase drugs could potentially interfere with fertility,
although this is still speculative.18
One drawback to the use of anti-telomerase drugs in the treatment of
cancer is the length of time needed for such drugs to have any effects.
If telomerase is not activated until numerous generations of cell division
have shortened telomeres to critical lengths, tumors cells could have
doubled thirty or more times before telomerase is turned on. Even if anti-telomerase
drugs were developed in the near future, they would need to be used in
conjunction with faster-acting anti-cancer drugs.19
Some researchers have theorized that telomerase might have an anti-aging
benefit, and that its use might delay the normal aging of cells by allowing
them unlimited reproduction. At this stage, however, the potential for
a pro-telomerase drug also promoting cancer seems too great to consider
it as an anti-aging treatment.20,21
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