Thursday, January 2, 2014

The Politicization of Top Scientific Journals --- Who Should I Trust? What Should I Believe?

It has become more and more often we are searching in vain through news channels or sources to try to find out which news agency is telling the truth, only to remember that the news has been brought by some big corporation, no longer owned by the independent spirit of Journalism. It is saying what their financial or political interests tell them to say, not necessarily the truth the public want to know. It has become more and more often we are hearing prestigious university professors, who we suppose to trust, talk like a politician, saying things that they have absolutely no scientific evidence or proof, saying things that the scientific data point otherwise, saying things that distort the scientific process but benefit themselves, saying things that they are not supposed to say as a scientist or physician. It is often the same group of prestigious professors who control those top scientific journals, such as Nature, Science, Cell, that the scientific community trusts most. It is often the same group of prestigious professors, often also editors of those top scientific journals or their close associates/friends, who get published in those top scientific journals with little or no peer-review. It is often the same group of prestigious professors, often also editors of those top scientific journals or their close associates/friends, who block the publication of others’ scientific breakthroughs that would have conflicts with their own research or interests. If there are multi-millions of grants, academic rank, salaries, job security, and lab spaces on the line, it is hard to imagine how much the scientific integrity and professional ethics would really weigh against those big material benefits, particularly under a confidential review system where the reviewers basically can do whatever they like, say whatever they want, even things far away from the truth, without any concerns to get caught.

The politicization of top scientific journals has not gone unnoticed in the stem cell community. It is not any secret to the scientific community that the biggest stem cell scam of the last few years is the induced pluripotent stem cells (iPS cells) made by the Japanese scientist Shinya Yamanaka who put multiple oncogenes into the skin cells, which was first published in Cell in 2007, widely proliferated in Nature, Science, Cell Stem Cell, and has become almost the only publishable fake stem cell research in Cell Stem Cell in the last few years, where most of the promoters of iPS cells are also the editors. It is not so difficult to tell in the first place that the idea of Yamanaka’s iPS cells is in fact flawed because it is common scientific knowledge taught in all the universities that cancer is caused by turning on oncogenes in adult cells, so iPS cells are actually abnormal cancer cells, not stem cells. Yamanaka’s iPS cells are actually the politicization of sciences by a group of prestigious university professors to meet Bush administration’s demand for alternative for pluripotent human embryonic stem cells (hESCs). Yamanaka’s iPS cells tell us a true story where science has become secondary to the political purpose, a true story of politicization of stem cell research. Yamanaka’s iPS cells were promulgated by more than 100 major international news agencies as the “biggest breakthrough of stem cell research”, as the “ethical alternative for human embryonic stem cells”. However, Yamanaka has never provided any scientific evidence that iPS cells are stem cells because it requires very difficult and time-consuming self-renewal analysis that is commonly accepted as the proof of any stem cells, nor anything else that Yamanaka or those promoters of iPS cells said about the iPS cells as the alternative for hESCs is true or has any scientific proof. There are many scientific reports to show iPS cells actually have more genetic defects than cloned embryos, which are known for abnormal. There are many scientific evidences to show iPS cells are actually flawed, however, these real scientific research and data were not so widely promulgated since they did not fit the political purposes of some interest groups. How did Yamanaka, who is the editor of Cell/CSC and also has close relationship with the presidents and other top officials of international society for stem cell research (ISSCR), skip the required self-renewal experiments and get his fake stem cell research published in Cell in 2007 without even providing the slightest scientific data for self-renewal that has been mandated for the proof of stem cells by anyone else? And how did Yamanaka win the Nobel prize with such fake stem cell research without any solid scientific evidences for any breakthroughs in 2012? It is interesting if we pay little bit attention to the timing of Yamanaka iPS cells and the timing of his Nobel prize as well as the scope of their promulgations by more than 100 major international news agencies as the “biggest breakthrough of stem cell research”, as the “ethical alternative for human embryonic stem cells”, which were all closely aligned with the political gains of those against hESC research. Scientifically, those flawed alternatives for hESCs, including Yamanaka iPS cells, later trans-differentiation of adult cells, and most recently cloned embryos, are disasters for stem cell research. If we look at how much taxpayers’ money has gone into such fake stem cell research or politicization of stem cell research of those interest groups, the magnitude is huge. Since 2007, about $5-10 billions of NIH (National Institutes of Health), CIRM (California Institute for Regenerative Medicine), and investor funds have gone into such flawed ideas, nothing has come out of it, except more and more reports to prove the flaws of such adult alternatives that were in fact flawed in the first place. Ironically, it is Obama administration, not Bush administration, has provided the most funding from NIH to those interest groups’ fake stem cell research or politicization of stem cell research by Bush administration. Needless to say, most of the beneficiaries are the promoters of iPS cells, many sitting on the editorial board of top scientific journals, including Cell Stem Cell, the official journal of ISSCR.

When it comes to tell stem cell scams from stem cell research, my more than 20 years of scientific training and knowledge have really helped me. Unfortunately, it is hard to say the same to the general public and investors who mostly do not have the same level of scientific knowledge to tell the truth from false about stem cell research. Maybe it would help if you pay attention to those warning signs, such as if the science has become secondary to the purpose, if the scientist or professor you think you trust talks like a politician, if the scientist or professor you think you trust is saying something without any scientific data, if the professor is talking about a big breakthrough but has absolutely nothing to show what the breakthrough is, if the physician or company is selling treatment or cure but has nothing to show that they can do that, if the company is saying their cells can repair heart but has nothing to show their cells can become heart muscle cells, if the professor begins to substitute data with some not so difficult drawings, etc. This opinion is written in response to reader’s suggestion below.

From: Lana Reese [mailto:lanamreese@gmail.com]
Sent: Tuesday, December 31, 2013 11:16 AM
To: contacts@SDRMI.org
Subject: New controversies in the Research/Publishing Process for Voive of Regenerative medicine readers

Hi

I hope all is well.

I wanted to pass along a couple links to stories that might be a good fit for Voive of Regenerative medicine, or could at least be valuable conversation starters for your social followings. It seemed particularly relevant given your position in quickly evolving field of stem cells.

Recently, Nobel Prize Winner Randy Schekman and former science editor Richard Smith called into question current practices of the scientific publishing process, underscoring a growing need for change. With these debates being such hot topics, I thought your readers would enjoy hearing your take on it, specifically the relevance that change could have for the industry moving forward.

Here are the links to the two stories, which delve into the problems and possible solutions facing scientific publishing:


Happy holidays and I’d love to see your opinion on the articles!
Best,

Lana

Editorial: The Designation of Human Embryonic Stem Cell Cardiac Therapy Derivatives for Human Trials

Editorial: The Designation of Human Embryonic Stem Cell Cardiac Therapy Derivatives for Human Trials

Dr. Parsons, founder of San Diego Regenerative Medicine Institute and Xcelthera, INC., has discussed scientific breakthroughs in human embryonic stem cell (hESC) research in her two recent Editorials, titled “Cellular medicine for the heart - the pharmacologic utility and capacity of human cardiac stem cells” at J. Clinic. Exp. Cardiology 2013;S11-e001 (doi: 10.4172/2155-9880.S11-e001) & “Reviving cell-based regenerative medicine for heart reconstitution with efficiency in deriving cardiac elements from pluripotent human embryonic stem cells” at Cardiol. Pharmacol 2013;2(3):e112 (doi: 10.4172/2329-6607.1000e112). Such breakthrough developments have demonstrated the direct pharmacologic utility and capacity of hESC cell therapy derivatives for human CNS and myocardium regeneration, thus, presented the hESC cell therapy derivatives as a powerful pharmacologic agent of cellular entity for CNS and heart repair.

Cardiovascular disease is a major health problem and the leading cause of death in the Western world. About 600,000 people die of heart disease in the United States every year–that’s 1 in every 4 deaths. The estimated costs of cardiovascular disease for the overall US population are approximately $190 billion annually. Currently, there is no treatment option or compound drug of molecular entity that can change the prognosis of cardiovascular disease. Given the limited capacity of the heart for self-repair or renewal, cell-based therapy represents a promising therapeutic approach closest to provide a cure to restore normal heart tissue and function for heart disease and failure. However, traditional sources of cells for therapy in existing markets have been adult stem cells isolated from tissues or artificially reprogrammed from adult cells, which all have the historical shortcomings of limited capacity for renewal and repair, accelerated aging, and immune-rejection following transplantation. In addition, artificially reprogrammed adult cells have the major drawbacks of extremely low efficiencies and genetic defects associated with high risks of cancers, which have severely limited their utility as viable therapeutic approaches. In the adult heart, the mature contracting cardiac muscle cells, known as cardiomyocytes, are terminally differentiated and unable to regenerate. There is no scientific evidence that adult stem/precursor/progenitor cells derived from mature tissues, such as bone marrow, cord blood, umbilical cord, mesenchymal stem cells, patients’ heart tissue, placenta, or fat tissue, are able to give rise to the contractile heart muscle cells following transplantation into the heart. Despite numerous reports about cell populations expressing stem/precursor/progenitor cell markers identified in the adult hearts, the minuscule quantities and growing evidences indicating that they are not genuine heart cells and that they give rise predominantly to non-functional smooth muscle cells rather than functional contractile cardiomyocytes have caused skepticism if they can potentially be harnessed for cardiac repair. Although a vast sum of government and private funding has been spent on looking for adult alternates, such as reprogramming and trans-differentiation of fibroblasts or mature tissues, so far, only human cardiac stem/precursor/progenitor cells derived from embryo-originated hESCs have shown such cellular pharmacologic utility and capacity adequate for myocardium regeneration in pharmaceutical development of stem cell therapy for the damaged heart.


Recent milestone advances and medical innovations in hESC research enable high efficient direct conversion of non-functional pluripotent hESCs into a large supply of clinical-grade high purity functional human neuronal cells or heart muscle cells for developing safe and effective stem cell therapies as treatments or cures for a wide range of neurological and cardiovascular diseases. Currently, these hESC neuronal and cardiomyocyte cell therapy derivatives are the only available human cell sources in commercial scales with adequate cellular pharmacologic utility and capacity to regenerate CNS neurons and contractile heart muscles, vital for CNS and heart repair in the clinical setting. Transforming non-functional pluripotent hESCs into fate-restricted functional human cell therapy derivatives or products allows moving stem cell research from current studies in animals towards human trials.