Charles Thornton, a professor of neurology at the University of Rochester (N.Y.), has received MDA support for research in myotonic muscular dystrophy (MMD, also known as DM) and other neuromuscular diseases. He's currently developing antisense oligonucleotides and small molecules for MMD. Thornton also co-directs the MDA clinic and directs the MDA/ALS Center at the University of Rochester Medical Center.
Margaret Wahl, MDA's medical and science editor, talked with Charles Thornton about his research.
Background note: The underlying cause of type 1 MMD is an abnormal expansion of repeated CUG chemical sequences in the genetic instructions for the DMPK protein. The underlying cause of type 2 myotonic dystrophy is an abnormal expansion of repeated CCUG sequences in the genetic instructions for the ZNF9 protein.
A: I think the important point is that there's strength in diversity, having different ways to come at the problem. MDA is supporting several research groups that are using different technologies to develop a treatment for the disease.
All of them are showing progress in one way or another in terms of having some of the intended beneficial effects when they're tested in cells growing in a dish or in a mouse that has some characteristics of myotonic dystrophy.
There might even be a reason to think that these things, if tried together, might have a stronger effect than if tried individually. That hasn't been tested yet, but it could be tested, down the road. There could eventually be combination therapies.
It's too early now to say which of the strategies in development is the best method. They all should be moved forward as efficiently as possible.
Note: Antisense oligonucleotides are molecules designed to target a specific chemical sequence, generally to block it or destroy it.
A: I'm not going to tell you what I'm going to vote for — small molecules or antisense. If I had to make a guess, I think the first one that will be tested in clinical trials is likely to be antisense because there are some shortcuts in the development process for that kind of drug.
A: Yes. There are different research groups that are trying different types of antisense. They come in different chemical flavors.
Antisense is a chain, and the types of antisense are different in terms of the chemical makeup of the parts that join the chain together — what people call the backbone or framework of the chain.
One approach is to use antisense as a guide molecule that shows an enzyme called RNase H where to make a cut in RNA. You pick the RNA that you want to cut, you design an antisense to couple with it, and then the RNase H cuts the target.
Note: RNA is a chemical derived from DNA that can carry genetic instructions for protein synthesis and can play other cellular roles. Abnormal expansions in the RNA for the DMPK protein underlie MMD1, and abnormal expansions in the RNA for the ZNF9 protein underlie MMD2.
A: Yes. When we did that, CAG25 was not making a cleavage in the target. It was binding to the RNA repeats, the toxic RNA, but not causing cleavage of it.
A: The CAG25 molecule, which resembles RNA, was designed to bind to CUG repeats, and to keep cellular proteins like MBNL1 [muscleblind-like protein 1] from getting stuck on the repeats.
A: Yes. The mice had toxic RNA with expanded CUG repeats in their muscle tissue. They were given injections of CAG25 into one leg muscle and injections of an inactive substance into the corresponding muscle on the other leg.
In the CAG25-injected muscles, the MBNL1 protein was freed up, which allowed it to do its normal job in the cell. The muscles treated with CAG25 showed several improvements in structure and function compared to the untreated muscles. In fact, myotonia — the prolonged muscle contraction seen in myotonic dystrophy — was eliminated in the treated mouse muscles.
Note: For more on CAG25, read MMD Research: 'Bright' Prospect.
A: Yes. That's the gapmer antisense work we presented at the International Myotonic Dystrophy Consortium in late 2011. That work was a joint effort with Isis Pharmaceuticals and Genzyme [now part of Sanofi].
Antisense can be RNA-like, or it can be DNA-like, or it can be constructed so that it's hard to say which it's like.
CAG25 is more RNA-like, but the gapmer antisense that we talked about at the conference is more DNA-like — and that's what RNase H is looking for. The job of RNase H is this: Show me where you've got DNA bound to RNA, and that's where I'll try to cut the RNA.
Actually, we didn't target the RNase-H-attracting antisense directly to the CUG repeats in our experiments. We targeted it to a part of the RNA strand that doesn't have the repeats.
An RNA molecule is like a long strand, and if you make a cut anywhere along it, so that it's no longer intact from head to tail, there's machinery inside cells that recognizes that and gets rid of the fragments that are generated by the cutting.
Picture a long piece of spaghetti. Put food coloring over one part of it, towards one end, and call that the expanded CUG repeats: That's the toxic part. If you take a knife and cut that spaghetti at any other place, the entire strand — including the part with the CUG repeats — will be unstable and easily nibbled up by other substances in the cell.
Note: For more on the 2011 consortium, see International MMD Consortium Includes Professionals, Families.
A: That's an important question about the safety of this approach. There's a possibility that the amount of DMPK protein made by the cell would go down even further than it already has. It's already somewhat reduced, and it might be further reduced, which might cause symptoms. Based on animal studies, we're not expecting that that would have strong effects, but we have to monitor this carefully.
A: The treatment showed some striking effects. We injected the antisense under the skin — systemically — so that it could circulate throughout the body. We gave the antisense injections twice a week for one month. We checked on the mice as early as one week after the injections, or as long as one year later.
After the treatment, we saw large reductions of the toxic RNA, elimination of myotonia, normalization of a process called RNA splicing, and no evidence of harmful side effects. RNA splicing is a process that MBNL1 participates in, so we assume that MBNL1 was free to do its usual job. A very surprising observation was that the antisense was still active up to one year after the last injection.
A: Yes. That study was directed by Andy Berglund, a biochemist at the University of Oregon. We helped out with the testing in mice.
Together with Dr. Berglund’s group, we found that pentamidine counteracted some of the effects of the abnormal genetic instructions in mice with an MMD1-like disease. The molecule appeared to inhibit MBNL1-CUG interactions, and there was improvement in some RNA splicing patterns. It was a partial effect, but it was an important start.
A big drawback with pentamidine is that it's fairly toxic. It would have to be chemically modified before it could be considered as a candidate for treating myotonic dystrophy.
That said, it's good to push forward on several different fronts at the same time. Several other groups of chemists are having success also.
Note: For more on pentamidine, read MMD Research: Disrupted Disease Process.
A: Not yet, but we're eager to do so.
A: It's a little bit different, but I suspect that a similar approach could be used in myotonic dystrophy type 2 to good effect.
A: It will have to be specifically put there. There is a therapeutic trial under way in which this type of compound is being delivered into the spinal fluid, for a condition other than myotonic dystrophy, and it's able to reach many parts of the brain. At first glance, this idea doesn't seem very practical, but I suspect that it might prove to have some important advantages.
A: It's too early to know, but I think there are reasonable prospects that this could also work in the heart.
A: I'm glad you asked that question, because I think that's really uppermost in people's minds. I would say that the hope that drives us every day is the possibility of having people take medication that will actually make them feel and function better.
From the experiments that have been done in animals, it's not unrealistic to think that that's a possibility, but we don't really know yet.