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Cloning is unsafe for the clone and surrogate
mother |
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The numbers are against survival |
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Dolly the sheep, first cloned mammal: 1 live birth out of 277 cloned embryos
(0.4%) |
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Cloned mice:
5 live births out of 613 cloned embryos (0.8%)
5 live births out of 314 cloned
embryos implanted (1.6%) (0.3%; 1 survived)
26 live births out of 312 cloned
embryos implanted (8.3%) (4.2%; 13 survived) |
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Cloned pigs:
5 live births out of 72 cloned embryos implanted (7%) |
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Cloned goats:
3 live births out of 85 cloned embryos implanted (3.5%) |
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Cloned cattle:
30 live births out of 496 cloned embryos implanted (6%) (4.8%; 24
survived) |
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Cloned cat:
1 live birth out of 188 cloned embryos (0.5%); of 87 embryos implanted (1.1%) |
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Cloned gaur: 1 live birth out of 692 cloned
embryos (81 blastocysts) (0.1%) (0%; 0 survived) |
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Cloned rabbits: 6 live births out of 1852 cloned
embryos (0.3%) (0.2%; 4 survived) |
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Cloned banteng: 2 live births out of 30 cloned
embryos implanted (6.7%) (3.3%; 1 survived) |
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Cloned mule (fetal cells): 3 live births out of
334 cloned embryos (0.9%) |
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Cloned horse: 1 live birth out of 841 cloned
embryos (0.1%) |
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Cloned rats:
3 live births out of 129 cloned embryos implanted (2.3%) (1.6%; 2
survived) |
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Even apparently healthy clones have gene
expression abnormalities.
*Humpherys D et al.; “Epigenetic
instability in ES cells and cloned mice”; Science 293, 95-97; 6 July
2001
*Humpherys D et al.; “Abnormal gene expression in cloned mice
derived from embryonic stem cell and cumulus cell nuclei”; Proc. Natl.
Acad. Sci. USA 99, 12889-12894; 1 October 2002 |
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A review of all the world’s cloned animals
suggests that every one of them is defective.
Ian Wilmut: “There
is abundant evidence that cloning can and does go wrong and no
justification for believing that this will not happen with humans.”
“Gene
defects emerge in all animal clones”, Sunday Times of London, April 28,
2002 |
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Health risk for the surrogate mother—“large
offspring syndrome” |
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Promises, Premises, and Published Data… |
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Claims unsubstantiated for embryonic stem cells |
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Current or potential embryonic stem cell
problems: |
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Difficult to establish and maintain |
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Difficulty in obtaining pure cultures in the
dish |
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Questions regarding functional differentiation
Sipione
S et al., “Insulin expressing cells from differentiated embryonic stem
cells are not beta cells”, Diabetologia published online 14 Feb 2004;
doi:10.1007/s00125-004-1349-z
Rajagopal J et al.; “Insulin
staining of ES cell progeny from insulin uptake”; Science 299, 363; 17 Jan 2003 Zhang YM et al.;
“Stem cell-derived cardiomyocytes demonstrate arrhythmic potential”; Circulation
106, 1294-1299; 3 September 2002 |
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Problem of immune rejection |
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Potential for tumor formation and tissue
destruction
Wakitani S et al.; “Embryonic stem cells injected into
the mouse knee joint form teratomas and subsequently destroy the joint”; Rheumatology
42, 162-165; January 2003 |
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Genomic instability
Cowan CA et al.,
“Derivation of embryonic stem-cell lines from human blastocysts”, New
England Journal of Medicine 350, 13; published online 3 March 2004
Draper JS et
al., “Recurrent gain of chromosomes 17q and 12 in cultured human embryonic
stem cells”, Nature Biotechnology 22, 53-54; January 2004
Humpherys S et
al.; “Epigenetic instability in ES cells and cloned mice”; Science 293,
95-97; 6 July 2001 |
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Few and modest successes in animals, no clinical
treatments |
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Ethically contentious |
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Current Clinical Uses of Adult Stem Cells |
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Cancers—Lymphomas, multiple myeloma, leukemias,
breast cancer, neuroblastoma, renal cell carcinoma, ovarian cancer |
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Autoimmune diseases—multiple sclerosis, systemic
lupus, rheumatoid arthritis, scleroderma, scleromyxedema, Crohn’s disease |
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Anemias (incl. sickle cell anemia) |
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Immunodeficiencies—including human gene therapy |
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Bone/cartilage deformities—children with
osteogenesis imperfecta |
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Corneal scarring-generation of new corneas to
restore sight |
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Stroke—neural cell implants in clinical trials |
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Repairing cardiac tissue after heart attack—bone
marrow or muscle stem cells from patient |
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Parkinson’s—retinal stem cells,patient’s own
neural stem cells, injected growth factors |
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Growth of new blood vessels—e.g., preventing
gangrene |
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Gastrointestinal epithelia—regenerate damaged
ulcerous tissue |
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Skin—grafts grown from hair follicle stem cells,
after plucking a few hairs from patient |
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Wound healing—bone marrow stem cells stimulated
skin healing |
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Spinal cord injury—clinical trials currently in
Portugal, Italy, Israel, U.S. |
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Arguments Against Human Cloning |
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No evidence that cloning is necessary or useful
for medical treatments |
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Cloning research will divert resources and delay
cures |
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Banning only implantation is unenforceable |
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Possible reproduction of living or deceased
persons without knowledge or consent |
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Confusion—kinship, parent-child identity,
parental expectations |
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Creates a class of humans who exist only as a
means to achieve the ends of others |
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Risking health and exploitation of women |
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Leading to commodification, commercialization of
human life |
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Gateway to genetic manipulation and control of
human beings |
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Unsafe, Unethical, Unnecessary |
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What does it mean to be human? |
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Person or property? |
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To whom do we choose to assign value? |
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Who will benefit? Who will decide? |
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