NEWSLETTER No. 126, MAY 2007

 

 

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EMBRYONIC STEM CELLS & CLONING FRAUDS

BABETTE FRANCIS

 

Remember the big cloning debate in our Federal Parliament? (See "Patterson's curse - the  Frankenbunny",  p. 5 of our Feb. 2007 issue).    Those of us who  opposed the cloning and destruction  of human embryos for  "research" were painted as uncompassionate right-to-lifers denying the sick and disabled  life-saving "cures".  The truth is  emerging:  embryonic  stem cells (ESCs) and "cloning" (which has yet to be achieved with human cells) are producing  no cures but lots of tumours in animal experiments.  What  ESC scientists are after is (a)  lots of research money from governments because there is little private investment, and  (b) removal of all restrictions on experimentation  on human embryos. 

The broadsheet press has been complicit in the cover-up.  There are frequent reports of  successful treatments  with "stem cells",  but one has to read to the end of the small print in the  article -  or guess - that the breakthrough is with adult, NOT embryonic  stem cells. 

In the US   the Democratic -controlled House voted 253-174   to expand federal funding for embryonic stem-cell research, but it fell  short of the 290 votes needed to override  President Bush's veto.  This is not a tragedy for the victims of disease and disability as painted by the  liberal media.  The real tragedy is that many states in the US have included funding for ESC research in their budgets, and this is taking money away from the field of  adult stem cell research from where the  cures are coming. 

Adult stem cells cure and treat more than 70 diseases and are involved in almost 1,300 human clinical trials. Scientists also keep discovering that adult stem cells are capable of producing a wide variety of mature cells.  Among the most promising developments was announced in the  January issue of Nature Biotechnology. 

Anthony Atala, director of the Institute for Regenerative Medicine at Wake Forest University  School of Medicine, reported that stem cells in the amniotic fluid that fills the sac surrounding  the fetus may be just as versatile as embryonic stem cells. At the same time they maintain all the  advantages that have made adult stem cells such a success.  This has caused some  consternation  on the part of those seeking increased taxpayer ESC funds because they  haven’t a   single clinical trial to boast about. Researchers admit they won't have approved ESC treatments for at least 10 years, if then. 

One advantage of  the claimed  advantages for ESCs  has been that most types of adult stem cells cannot be multiplied outside of the body for very long, while embryonic ones may replicate in the lab indefinitely. But Atala's new amniotic stem cells grow as fast outside the body as embryonic stem cells (doubling every 36 hours), and he's now been growing the same cell line for two years, with no indication of slowing. 

That leaves ESCs with only one “potential” advantage  - they can be "differentiated" into all three "germ layers," or subtypes of cell. That means they should be able to be made into all of the 220 types of cells in humans. For a long while, adult stem cells were believed to be only capable of differentiation to a limited number of mature cells, depending on the type of adult stem cell with which you start. For example, a marrow cell could become any number of types of marrow or blood cells, but it couldn't become a muscle cell. That's a different germ layer.

 

Adult stem cells exist in many tissues including blood, skin, fat,muscle, brain, dental pulp andhair follicles.

However,  experiments around the world have  shown that adult stem cells from one germ layer can be converted into those of another in a living human, such as those that turned marrow cells into heart muscle and blood vessels in live humans.   Amniotic stem cells may be the most easily differentiated of all - as well as among the easiest to extract in large amounts.  Indeed, they are routinely recovered with a hypodermic needle during amniocentesis. While it's widely believed that this procedure slightly increases the chance of miscarriage, a sizable study last November of 35,000 women who underwent mid-trimester testing found "no significant difference in loss rates between those undergoing amniocentesis and those not undergoing amniocentesis." 

There are over four million births each year in the United States (around 250,000 in Australia), and  Atala calculates that merely 100,000 amniotic stem cell specimens could supply 99 percent of the U.S. (300-million)  population's   needs for perfect matches for transplants, assuming  a perfect match is even needed.  About 700,000 amniocentesis procedures are performed in the United States and Western Europe each year.  Amniotic cells can also be obtained at the time of birth when the membranes around the amniotic sac rupture. Women describe this as their “waters breaking”. 

Of course  ESC researchers have downplayed the Atala findings. The work will "still require a lot of replication from other groups before they can be conclusive," Stephen Minger,     a lecturer in stem-cell biology told a British newspaper. "They have only shown that these particular stem cells can turn into a couple of different types of other stem cells .... a lot more work is required." Other media outlets would say the same. Newsweek International claimed, "Many scientists are quick to emphasize that comprehensive human trials are still many years away." 

The New York Times (there's the NYT again  - see  Media Bias on p 13 )  refused even to allow people to read between the lines - they simply never reported the news about Atala's work. When a reader complained to the "Public Editor,"  about the omission, the Times responded that its genetics reporter, Nicholas Wade, "looked at the Atala paper last week and deemed it a minor development." Wade said of the paper, "It reports finding 'multipotent' stem cells in amniotic fluid. Multipotent means they can't do as much as bona fide embryonic stem cells (which are called 'pluripotent')." 

Minger,   Newsweek and  Wade are wrong. As Atala told PBS's Online NewsHour, "We have been able to drive the cell to what we call all three germ layers, which basically means all three major classes of tissues available in the body, from which all cells come."   The online abstract of the Atala paper indicated the same. Of course, this is the same paper that told readers in 2004 that there were no cures or treatments with adult stem cells. Not  the 70 cures or treatments, some dating back half a century, but   none! 

The media cover-up is obvious.  Atala's work actually is a replication of numerous studies. He's just taken the research further and drawn his cells from amniotic fluid, whereas others have drawn the identical cells from  placentas. Amniotic and placenta stem cells are the same, as Atala himself noted.  Rather than  human trials being "many years away," trials were being carried out  many years ago.   The New England Journal of Medicine carried one paper on a placenta stem cell trial back in 1996 and another paper two years later. There's been an ongoing clinical trial since 2001 to treat sickle cell anemia. 

The Washington Post's  Rick Weiss, who has been accused of  promoting ESC research, tried to find a middle ground.   [You know, like Hillary Clinton trying to find a middle ground on abortion by  promoting  the Morning After Pill].  He  wrote that  "The new (!) cells are adding credence to an emerging consensus among experts that the popular distinction between ‘embryonic’ and 'adult' stem cells -  those isolated from adult bone marrow and other organs - is artificial." 

That is  rubbish.   It is not an artificial distinction that extracting  ESCs kills the embryo while   adult stem cells can be obtained without killing the donor.  That distinction remains no matter how liberal journalists attempt to obscure it or what the “potential” of embryonic stem cells is.  

What is somewhat   artificial  is the term "adult stem cell," which was appropriate   when all adult stem cells were  taken  from bone marrow, but  this is confusing now that they are  being extracted from placentas, amniotic fluid, and umbilical cords, which aren't   "adult" sources. But for discussions both scientific and moral, stem cells can still be  classified as  embryonic and  non-embryonic.   

All embryonic stem cell treatments  tend to  result in tumours;   they require permanent, dangerous, immunosuppressive drugs because the body rejects them as foreign and they are difficult to differentiate into the needed type of mature cells. Non-embryonic stem cells, however, do not become cancerous; they are far less likely to cause rejection (especially the youngest, including umbilical cord and amniotic/placental cells) and they have been used therapeutically since the late 1950s (originally for leukemia) because they have the amazing ability to form the right type of mature cell merely upon being injected into a body that needs that type of cell.

It is these biological differences that have held ESC  research back, not  lack of  "compassionate" legislation, lack of funds  or mean  right-to-lifers.  Stem-cell researcher Malcolm Alison of the University of London told the Daily Mail that amniotic cells "appear to be at least as malleable as embryonic stem cells but without all the ethical baggage." 

There is another moral issue.  Research funds are not unlimited and  non-embryonic stem cell researchers are already achieving amazing results  such as growing new heart and liver tissue and treating multiple sclerosis - all in living humans. Just this year there have been reports of   brain cells that regenerate in humans  opening up the potential for treatments of brain diseases, and there have also been trials of adult and umbilical cord cells for treatments of juvenile diabetes. 

There is no justification for wasting one more cent on embryo killing ESC research other than to feed the egos of amoral scientists.  Our money should be spent on adult and other tissue stem cells (amniotic, placental, umbilical cord)  which are producing  results, and on other areas of ill-health  not connected with stem cells, such as treatments    for heart disease and cancer.

 

Very Premature Baby Leaves British Hospital, Sparks Abortion Debate

LifeNews.com reports from  England that a   second very prematurely born baby to overcome long odds and survive has made the news and her survival is sparking a debate over whether or not to limit late-term abortions. Tiny Millie McDonagh has stunned the medical world by beating doctors' expectations and going home after being born four months premature.

Millie  was given just a one percent chance of surviving after she was born at 22 weeks into  the pregnancy. At birth, the little girl weighed just 20 ounces (570g) and was only 11 inches (28  cm) long. Millie is one day older than Amillia Taylor, the premature baby born in Miami who has received national and international attention in recent days. The newspaper reports that Millie's parents, Tommy McDonagh and Natalie Matthews, are finally now able to take their daughter home -- four months after she was delivered. Millie received medical attention in the  intensive care unit of St. Mary's Hospital in Manchester following her October birth and she now weighs five pounds. She will need oxygen for a while to help her breathe but her  physicians now say she will suffer no long-term health problems from the premature birth.  

In Melbourne the Royal Women’s Hospital is commendably undertaking a program to help parents bond with their very premature infants, including infants with genetic disabilities.  However in another section of the RWH, babies of the same gestational age - or similar disabilities - are aborted.

Write to the RWH pointing out their inconsistencies.

 

 

 

 

 

 

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