Anti-aging molecule successfully restores multiple markers of youth
newatlas.com
newatlas.com
Plus perhaps you can have a "rejuvenation session" with TERT instead of boosting it forever. Thing seems like it can work after TAC is no longer being activated for quite some time.
Ultimately though yes, it may increase the number of cells that have already taken multiple hits if multiple hit cancer hypothesis is really true.
https://pubpeer.com/search?q=depinho
Edit: For those who aren't familiar with PubPeer, it's a platform for exposing research fraud and criticisms of research papers. This particular researcher is well known on it.
Recent research has challenged the notion that longer telomeres are universally beneficial, revealing a complex relationship between telomere length and cancer risk. Having excessively long telomeres is indeed related to an increased cancer risk, primarily because it prevents the natural selection against potentially cancerous cells[1][3].
Key findings from recent studies include:
1. People with mutations leading to abnormally long telomeres have a higher risk of developing various cancers, including melanoma, thyroid neoplasms, and blood-related cancers[1].
2. Long telomeres allow cells to accumulate more mutations over time, as they can divide more times before reaching critical telomere shortening[1][3].
3. The telomere tumor suppressor pathway, which normally helps prevent cancer by limiting cell division, is less effective when telomeres are too long[4].
4. Families with mutations in the TINF2 gene, which regulates telomere length, show a higher incidence of various cancers, including breast, colorectal, and thyroid cancers[4].
5. Genome-wide association studies have identified both rare and common genetic variants that lengthen telomeres and are strongly associated with increased cancer risk[3].
These findings suggest that while short telomeres can lead to premature aging and organ failure, excessively long telomeres may provide a permissive environment for cancer development by allowing cells to proliferate beyond normal limits[1][3][4].
[1] Long telomeres may heighten cancer risks https://www.nih.gov/news-events/nih-research-matters/long-te... [2] Link Between Long Telomeres and Long Life Is a Tall Tale, Study ... https://www.nytimes.com/2023/05/04/health/long-telomeres-age... [3] Long telomeres and cancer risk: the price of cellular immortality - PMC https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6715353/ [4] Telomere shortening protects against cancer https://www.rockefeller.edu/news/29625-telomere-shortening-p... [5] Mice with hyper-long telomeres show less metabolic aging ... - Nature https://www.nature.com/articles/s41467-019-12664-x
I assume that before applying the drug you'd check the mean telomere length, which is easy enough to do.
You probably wouldn't give it to people with actual active cancers either, and check for anything unusual afterwards, to handle with properly targeted poison. (AKA chemotherapy, and resulting cancers would be super early stage so easy to quash)
>"It is encouraging, however, that long- term TAC treatment was well tolerated without any overt or his- tological adverse effects including carcinogenesis. Nonetheless, additional safety studies in non-human primates are warranted. Along these lines, it is worth noting that TAC may reduce cancer incidence, given that insufficient telomerase resulting in telomere dysfunction coupled with loss of p53-dependent DNA check- point control is a major driver of chromosomal instability and cancer genesis in the aged. 53 Correspondingly, TERT reactiva- tion in aged inducible-TERT mice was shown to reverse aging phenotypes without causing an increase in cancer."
We could be in a similar situation with anti-aging drugs. Plus, with citizen science projects making ad-hoc labs more accessible than ever, there's a good chance that normal people could make their own versions of these anti-aging drugs, assuming that science journals and informatic pipelines remain accessible (the current rent-seeking of top journals lends some small but worrying evidence against this).
0: https://en.wikipedia.org/wiki/Craig_Venter#Human_Genome_Proj...
Sadder day for those who only sees tragedy in progress.
EDIT: Had forgotten for a second that we can know ask this kind of questions to a computer, "straw man argument".
Yeah, who needs "X". I won't even bother with the "the rich" stuff, because, frankly, it's too tired, pathetic, childish and naive.
Crazy, I know.
How would I be able to enforce it? By somehow keeping the costs high? By lobbying?
Nothing would work, because this would be too big for the working class to just sit there and watch, and if lots of people get really pissed, it can turn very ugly, as history has taught.
People will want it and they'll get it, one way or the other.
So you might have doddering 120 year old ancients (potential predicted life extension) with ever more brain damage.
https://rickroderick.org/302-heidegger-and-the-rejection-of-...