Age A Byproduct of Cancer Defense?
A reader writes "The International Herald Tribune has an article which says, in brief: they have discovered that aging in mice seems to be a byproduct of the chemicals that prevent cancer" If true, that's quite a double edged sword - avoid death, to cause it later.
Man o man are these guys in for a surprise:
:-)
http://www.google.com/search?q=anti-aging+pills
Especially these folks:
http://www.pure-milk-calcium.com/immunocal.htm
This product is supposed to prevent cancer by extending your life
In the environment where we did most of our evolving very few people lived to "old age" before succumbing to a number of other dangers, so something that kept cancer at bay for a while at the price of guaranteeing death after a few decades probably seemed like a good deal. Kind of like the 640k limit. "That ought to be enough for everybody."
Actually, I was trying to be Insightful, not Funny.
Chemicals that prevent or help prevent cancer usually tamper with cell division. If cellular division is in some way interrupted or affected by anti-cancer agents, then aging more than normal can easily occur. It goes back to one's preference. Long, suffering life or short, fulfilled life?
Job? I don't have time to get a job! Who will sit around and bitch about being broke and unemployed then?
This sort of puts a whole new spin on this whole "Cure for Cancer" thing. The study seems to suggest that cancer is inevitable, and any attempts by our body to avoid it result in our own death.
Seems to me that if this is the case, it would have some serious repurcussions on how we currently understand how our bodies work. What is it about our physiologies that makes cancer such an irresitible force?
It hurts when I pee.
Is Alex Chiu's miracle Eternal Life Device going to give me cancer now? I can't believe it! The man is a fraud!
This goes against everything I've ever been taught. I'm beginning to put more and more stock in that time cube thingy every day....
"Too much p53 and you get this aging effect. Too little and you get cancer. My guess is that evolution has evolved just the right level."
Would somebody explain to me how evolution would play in this finely-tuned scenario? In the U.S. our average lifespan is over 70 years, yet most women pass menopause around age 45. There's a 25 year lifespan discrepancy, in which evolution has no effect, because the population (at least of women) can't reproduce!
Does this mean that since modern day man has increased contact with carcinogens, evolution will now favor those with higher cancer resistance and therefore shorter life-spans?
"when the going get's wierd the wierd turn pro." -hst
The average lifespan is only that long thanks to modern advances in medicine, disease cures, etc. Without them, the average human could expect to live maybe 50 years, although menopause might also come a little earlier.
But you can't think of those years as being wasted. After all, if a woman has children as late as 40, she'd certainly like to raise them to adulthood (and then help them learn to raise their own children) before she dies.
she's been 35 years old for about 10 years now.
Bill Clinton: Pimp we can believe in. - The Shirt!!!
It has now been discovered that the leading cause of cancer in labratory mice is.....
Scientists!
Please take note and live you life accordingly.
Papa Legba come and open the gate
You could think of death as the end of cell growth, whereas cancer is cell growth gone out of control.
Silly mortals! I propose that whomever designed us intentionally created these apparent paradoxes to force all doubters to eventually believe.
"What is the sound of one belly slapping?"
Ancient texts with people thousands of years old are explained by the lack of digital watches.
:)
Seriously, its the product of an oral tradition. Ever play the telephone game?
I've read that in cancerous cells, the telomeres don't shorten each time the cell divides, so there's no system in place to stop the cell from dividing forever (and all of it's children cells, etc.).
A reasonable hypothesis for why controlled growth through telomeres is necessary is to prevent mutations from a long series of copies (copies of copies, etc). This way, a "series" of cells only last for a fixed number of generations. After so many, the series stops. Then the stem cell(s) can take over and start a new "first generation" cell which can be the start of a new series of cells.
As we get older, perhaps the stem cells themselves start to degrade or become mutated (possibly causing cancer), and are no longer able to produce good "first generation" cells. As an example, this could be why we develop skin blemishes as we get older. Just imagine what's happening to other genetic attributes.
It's my personal theory that the process of aging is actually just the process of various parts of our body mutating to a small degree. For example, one little DNA pair mutated in a skin stem cell, and suddenly you have a freckle.
I always figured that given the knowledge that's taught in regular high-school biology, most people could figure out that the tradeoff of preventing aging is the increased risk of cancer (since cancer cells could go on forever if supplied with the nutrients necessary for cells to live).
*shrug* I dunno...
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I'm speaking here as founder and president of what was the 2nd largest biotechnology company in the U.S. focused on the molecular biology of aging during the mid-'90s. So we will assume for the sake of improving the discussion I'm moderately well informed in this arcane branch of knowledge.
Point #1: If you read something scientific or technical in the "popular" press, never assume that they managed to interpret it properly. If reporters don't have an education in a particular discipline, they are not likely to understand the subtleties of what is being discussed. Always go back to the most scientific sources you can get access to. Most of the readers are presumably qualified to evaluate arguments on technical merits (this is the /. forum!). Learn the jargon and if you don't understand something find an expert and ask questions (or post to the forum -- you never know when an expert might be lurking).
Point #2: Never assume a /. poster knows what they are talking about (or has verified what they may have copied or concluded from popular press). Case in point: "aging in mice seems to be the byproduct of the chemicals that prevent cancer". The material under discussion is a mutant p53 protein which is the byproduct of a modified p53 gene. It is not by anyone familiar with discussions in this field a "chemical". The p53 protein weighs tens of thousands of daltons and has multiple "active" functions -- most molecules considered "chemicals" weigh less than a few thousand daltons and have few, if any, "active" functions.
From the Nature news report: "they created mice with a chunk missing from one copy of the gene". Translating this into "programmer" terms -- this is in effect replacing 1 of 2 instantiations of an essential subroutine in an ~30,000 subroutine system with a subroutine that has had some of its lines deleted. How do you draw conclusions as to what is going on in that situation? Unless you know what lines were deleted and what the purpose of those lines was you have relatively little hope of drawing conclusions that would allow you to debug the system (at least IMHO). You certainly cannot discuss what the situation means in any intelligent fashion.
All of that being said, I'll provide my "spin" on the results. The normal p53 protein is a "gatekeeper" protein. Its purpose is to determine whether or not DNA damage is present (i.e. whether your program has been corrupted). If too much damage is present it induces cells to commit apoptosis (cellular suicide). If less damage is present, it delays cellular replication (copying) until the damage that is present can be repaired (calling the ECC subroutines). So it acts as a brake on the replication of mutated/damaged DNA and an executioner for cells that are so far beyond the error-correction subroutines that they represent a threat to the entire organism. In larger organisms (which have more cells and are therefore at greater risk of developing a "mutant" program and therefore cancer [which is unregulated cellular replication]) it is important to constrain replication. So humans, in contrast to mice may have a p53 which strongly constrains cellular replication. { Alternatively they may have "redundant" subroutines like telomere shortening (mice have very long telomeres, humans do not) which function as "backup" programs that function to limit cellular division and therefore the development of cancer. (This is based on the concept that short telomeres inform cells to "stop dividing" just as "damaged DNA" [through the p53 protein] cause cells to stop dividing.) } The extent to which short telomeres may resemble "damaged" DNA (and therefore activate the p53 "subroutines") is unclear (to me) at this point. [This is a fairly hot topic of scientific debate.]
If we view cancer and aging as complementary ends of the see-saw -- allow too much cellular replication and one gets cancer -- allow too little cellular replication and those parts that wear out are not replaced, resulting in aging, and one may be able to interpret the results of this study. The part of the p53 gene that was deleted probably served to function to "remove" the block against replication or "enable" the replication function. So what may be occuring is that the mutant p53 gene may be detecting damage, blocking replication, but then when the damage is repaired the defective p53 may not be allowing replication to proceed. Thus you have very effective anti-cancer properties but as one gets older there are fewer and fewer cells available to replace those that are lost. Net result: accelerated aging.
Now, this result need not be pessimistic. As Tom Kirkwood, one of the world's leading gerontologists pointed out in the Nature article, "We could be able to pick a path through the molecular mechanisms of ageing without making cells more tumour-prone. 'There's no reason why you shouldn't get greater defence against cancer and greater longevity.'"
As a once upon a time programmer -- I encourage people in the software industry -- "View genomes as programs -- lets figure out where the bugs are and then lets go fix them."
The reason being that thermodynamics (or chaos theory, or whatever) says that you're wrong. Any system as complex as a living cell, even something so simple as a yeast cell or E coli can not maintain that level of organisation for long. The cell is very thrifty with its organization, to be sure, but it is not infinitely so. That's why reproduction and evolution are so critical, because no single system can survive by itself for too long, so it must rebuild itself from scratch. Yes, you can put these systems in to hibernation, but that isn't really life functioning in any way shape or form until it's revived.
And of course pre-programmed cell death wasn't present in single cell organisms, it'd be counterproductive for an E coli to simply kill itself. Preprogrammed cell death does not kill the entire organism, and it obviously be detrimental if it did.
And as for sex and evolution evolving together, there are single celled organisms that have sex via plasmids. Granted, it might not be the "one chromosome from each parent" that we are used to in humans, but it is still genetic exchange by conjugation. There is no apoptosis here either.
"I may not have morals, but I have standards."