After seeing the articles:
http://onlinelibrary...200245/abstract
Above all and linked to above:
http://onlinelibrary....201200246/full
http://www.ncbi.nlm....les/PMC3057569/
There is clear evidence that increasing the exp
ression of TERT is achieved rejuvenation and prolong youth without involving significant increase in tumors.
There are also investigating Maria Blasco by adding 3 TERT genes and and other 3 of TP53 genes in mouse embryos with a more significant increase of life and the period of youth of the same
Linking it with the information I stated in previous posts in this thread in this group I thought maybe if used gene therapy to increase not only TERT but the entire set of genes involved in longevity and prevent cancer could obtain a lengthening of the youth much higher and greater health
So as to
1 - avoid damage
2 - expressing TP53 (which regulates the repair, celullar apoptosis, prevents cancer for cell exp
ression of TERT in previously damaged, regulates cell differentiation and decides to repair tissues and parts of bodies as the length of telomeres with the cells involved)
3 - repair damage
4 - safely extend telomerase
5 - differentiate tissues and repair tissues, organs, even replacing lost limbs with good quality fabric and it does not scar but this involves a large loss of telomeres by the number of copies
The idea would be to add in the gene therapy virus
to 1:
Msn2
Msn4
SOD1
SOD2
SOD3
Glutathione
to 2:
TP53
(And in any case for 3, 4 and 5)
to 3:
BanF1
Sirt1
for 4:
TERT
to 5:
MyoD1 (Myostatin antagonist) MyoD and TP53 (p53) related and mutually regulated by p21 and this is associated with tumors
MSX2 homeobox (and / or Wnt glycoproteins)
But goes a very long list and many tests ahead before deciding.
I see it elsewhere:
http://www.limm.leed...ups/melcher.htm
What has driven me to the idea of getting antibody antagonists:
1 SCH9
2 mdm2
3 mTOR serine / kinase theronine
4 PinX1
5 Myostatin
cerberus?
Antibody being tested design and are indicators could be used for research
I have thought that one of the viruses in gene therapy (such as VV9) could be added not only or not add extra copies of genes to be expressed in quantity but also more or exclusively sequences of antibody genes Design inhibited.
So I guess you could add more copies of TERT, TP53 more copies, more copies of BANF1, more copies of Sirt1, etc. But it could add copies of antibody against mTOR serine / kinase theronine or copies or copies antibody against mdm2 antibody SCH9 against
This could not add antibody PinX1 if it looks clean and add copies of TERT or add copies of antibody BANF1 and SCH9.
Or add copies of antibody against myostatin (antibody is designed under name myo-29 for the treatment of muscular dystrophy) and copies of MyoD1 but there are problems of cancer, or MSX2 homeobox add copies of the liver as the rest of the body to regenerate, but you can control the Wnt glycoproteins correctly and with this the highest exp
ression of TERT preventing age to regenerate tissue lost a limb.
A view that seems
Shilima khemen