89 posts categorized "Research"

January 26, 2012

Good news for hESC trials: transplanted human embryonic stem cell-derived retinal pigment epithelium… and it’s safe!

by Angela C.H. McDonald

IStock_000012475983XSmallAs has been reported broadly this week, transplantation of human embryonic stem cell-derived retinal pigment epithelial cells appears to be safe in human patients, and it may even be efficacious (although this can only be confirmed via a Phase II trial). 

Advanced Cell Technology (of California) published a preliminary clinical report of their Phase I clinical trials online this Monday in the Lancet. The two Phase I clinical trials were initiated at UCLA’s Jules Stein Eye Institute in July 2011. These trials aimed to treat Stargardt’s Macular Dystrophy and Dry Age-Related Macular Degeneration (two major causes of blindness in the developed world). Each trial will enroll up to 12 patients, with a safety endpoint at 12 months. Four months following transplantation, no adverse affects such as tumorigenicity, ectopic tissue formation, inflammation or cell proliferation could be detected in patients.

The subretinal space of one eye in each patient was injected with retinal pigment epithelial cells generated from human embryonic stem cells. The retinal pigment epithelium is a single cell-thick protective layer in the eye. In the eye of a macular degeneration patient, retinal pigment epithelial cell degeneration causes dysfunction of photoreceptors (which sit on top of the retinal pigment epithelium) and vision in that area of the eye is lost.

Although visual acuity assessments revealed functional improvements in the transplanted eye of each patient, these results should be interpreted with caution. While the Stargardt’s Macular Dystrophy patient only showed improvement in the transplanted eye, the Dry Age-Related Macular Degeneration patient showed improved visual function in both. However, the injected eye did show more improvement than the non-treated eye.

Despite the fact that Monday’s report is very preliminary (results from only two patients at the four-month mark), the company must have a great deal of confidence in the trial for it to have made this public announcement. Additionally, Advanced Cell Technology announced in a press release published on their website Monday that patient enrollment has now begun in the UK for a Phase I clinical trial for Stargardt’s Macular Dystrophy and the first patient was treated in London last Friday.

This exciting news comes just two months after Geron’s announcement to end the first ever FDA-approved human embryonic stem cell Phase I clinical trial, a move described as a strategic financial decision by Geron (covered in a previous blog entry). Disappointment and controversy surrounded the sudden halt of the Geron trial and some question the motive behind this decision. Some speculate that a lack of efficacy in this safety trial is what lead Geron to pull the plug.

Although it felt like the stem cell community took a number of hits in 2011 (including the shut down of the Geron trial and the prohibition of patents for human embryonic stem cell products by the EU), it seems that 2012 is off to a great start. 


January 24, 2012

The “Viagra effect”: how known drugs can be repurposed to target cancer stem cells

by Paul Krzyzanowski

Repurposing known drugs for new applications is a strategy with fascinating potential, with two of the most notable examples being Thalidomide and Viagra. Thalidomide was commonly used in the late 1950s as a sedative in pregnant women, later being associated with serious birth defects. Today, it is used to treat multiple myeloma. Viagra was being developed by Pfizer to treat high blood pressure when its ability to ‘treat’ erectile dysfunction was identified as a side-effect, resulting in a complete shift in marketing strategy.

The major allure of finding novel uses for existing drugs is that the long process of early Phase I clinical trials can be sidestepped, as the drugs are already known to be safely delivered. This approach decreases the overall cost of developing drug candidates and brings the development of treatments for rare and neglected diseases closer to reality.

The principle of identifying a drug candidate is straightforward: take a large number of different chemical compounds and test each one for some desired activity. Small molecule screening has long been used by pharmaceutical companies to identify potential drug candidates for probably as many disease conditions as there’s a market for.

Continue reading "The “Viagra effect”: how known drugs can be repurposed to target cancer stem cells" »

January 06, 2012

Sifting through all that monkey business

by David Kent


Yesterday, a landmark paper emerged from Cell which reported two major findings to the scientific community:

  1. Primate embryonic stem cells cannot generate chimeras, and 
  2. Aggregation and injection of multiple early-stage four-cell primate embryos (not embryonic stem cells) can form chimeras. 

Together these findings underscore a fundamental difference between rodent and primate embryonic stem cell lines and show that generating primate chimeras is possible.

As you might expect, this article was heavily publicized (e.g.: The Guardian, The National Post, and the BBC) but it seems that all of the reports focus on the generation of a monkey chimera and not on the more challenging question for scientists that results from not being able to do this from embryonic stem cells. Much of our understanding about embryonic stem cells comes from studies in lower order animal models (frog, mouse, sheep, etc.) and scientists sometimes tacitly assume that this process operates similarly in humans. This not only has major implications for our understanding of early development, but also substantially impacts the struggle to bring stem cell derived therapies and treatments into the clinic.   

Continue reading "Sifting through all that monkey business" »

December 21, 2011

Whose life is it anyway? Building patient needs and goals into stem cell clinical trials

by Lisa Willemse

IStock_000018269221XSmallIn a traditional view of medical research, advances tend to be measured against the overarching goal of cure. Noble as this might be, research is rarely such a black and white affair -- if we have learned anything, it’s that there are innumerable shades of grey.

Even the goal itself can be questioned, especially when achieving it could be 50 years into the future.

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December 14, 2011

17-year-old high school student makes a cancer stem cell breakthrough

When we report on breakthroughs in stem cell research, we typically link to well-funded studies published in peer-reviewed journals by world-renowned scientists. This time, it’s a little different.

Angela Zhang, a high school senior from Cupertino, California, was awarded a $100,000 scholarship for her submission to the 2011 Siemens Competition in Math, Science & Technology: A “gold and iron oxide-based nanoparticle” designed to seek out and destroy tumour-causing cancer stem cells.

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December 13, 2011

The apple of a bioengineer’s eye: mature photoreceptors

Apple of a bioengineer's eyeby Angela C.H. McDonald

Last spring, I wrote about the remarkable generation of self-organizing retinal tissue created from mouse embryonic stem cells. The study successfully created all major retinal components including photoreceptors, albeit at a low abundance. However, while multi-layered optic tissue did form, the alignment and organization of mature retinal cell types differed from that of the mouse eye in vivo.

The missing ingredient in this experiment was a physical, instructive cue to direct retinal cells into the complex structural pattern of the eye. 

A recent paper published in Biomaterials by another group of researchers described a biomaterials-based approach for creating organized photoreceptor cells from human embryonic stem cells.

Human embryonic stem cells were differentiated into retinal cells and seeded onto a specially designed scaffold positioned on top of a retinal pigment epithelial cell layer. This resulted in the organization of cells into a complex retinal architecture.

Continue reading "The apple of a bioengineer’s eye: mature photoreceptors" »

December 06, 2011

Tick, tock, clock – the clock is ticking for you

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Please read this article on its new home, Signals BlogTick, tock, clock – the clock is ticking for you

November 29, 2011

Unsolved mysteries in the intestinal crypt

by Angela C.H. McDonald

Crypt_dungeonsmThe intestine is an amazing organ. In fact, when I am not reading research related to my thesis, I read about the stem cell population that maintains our gut, the intestinal stem cells (ISCs). And sometimes, the reading reveals most unusual mysteries. 

ISCs have their work cut out for them. They must renew the lining of our intestines every few days throughout our lives. ISCs reside in a niche located somewhere within the glands that line our gut tissue (also known as intestinal crypts) however; much speculation and controversy has surrounded the exact identity and location of the ISCs. 

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November 23, 2011

Early data promising for first clinical trial using human cardiac stem cells

by Ben Paylor

A week of highs and lows for the global stem cell community brought with it a healthy dose of optimism for cardiac stem cell researchers. Pilot data from Dr. Roberto Bolli and colleagues’ landmark SCIPIO (Stem Cell Infusion in Patients with Ischemic CardiOmyopathy) clinical trial, published in The Lancet last week, provides much needed new momentum for the therapeutic potential of cardiac stem cells (CSCs).

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November 17, 2011

Not all doom and gloom: Major investment in UK stem cell therapy initiative

While many researchers will feel disheartened by last month’s ruling in the Court of Justice of the European Union that prohibits scientific research patents on human embryonic stem cell products (see Ubaka Ogbogu’s article), it seems some positive news is emerging from Europe as well. Specifically, the United Kingdom has recently promised a huge investment in the development of a major cell therapy centre.

In an effort to emerge from the recession, the UK government has launched a program through its Technology Strategy Board that will create a series of Technology and Innovation Centres. Building off David Cameron’s 2010 announcement, the investment is not trivial (£220 million or ~$350 million) and the idea is to take advantage of the UK’s strengths in various research sectors to build an environment of business development mixed with research advances and opportunities.

The cell therapy centre will build on the UK’s expertise in stem cells and regenerative medicine and is described as “a unique centre where academics, businesses and clinicians (i.e. medical professionals with a special interest in cell therapies) will work together to focus on the commercial development of cutting edge technologies in cell therapy.” According to a recent article in the Guardian the centre has already gained the support of major multinational pharmaceutical companies such as Pfizer, GSK, and Astra-Zeneca, which should provide a good base of investment for such a lofty project.

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