Two birds, one stone: HTT-lowering drugs also target CAG expansions

Huntingtin (HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15)-lowering and somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. have been two of the hottest topics in Huntington’s disease (HD) research in the past decade. Recent work from a team at Massachusetts General Hospital detailed a serendipitous overlap between the two – certain HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering drugs can also help regulate the ongoing CAG repeatCAG repeat The stretch of DNA at the beginning of the HD gene, which contains the sequence CAG repeated many times, and is abnormally long in people who will develop HD expansion. Seemingly, this could allow researchers to kill two birds with one stone using a single drug. But there’s more to this story.

CAG expansion causes toxicity

The CAG repeatCAG repeat The stretch of DNA at the beginning of the HD gene, which contains the sequence CAG repeated many times, and is abnormally long in people who will develop HD within the HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 gene is the nefarious player leading to HD. This repeat can expand in some cells over time, which is the biological phenomenon known as somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain.. We’ve talked a lot about somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. lately, which you can read more about in this recent article.

A current hypothesis for how the CAG expansion that causes HD makes people sick is a 2-step process. In this model, first, the inherited CAG length slowly expands in some cells over time. Second, once the CAG length reaches a threshold, toxicity in the cell is triggered, leading to death. This process doesn’t appear to occur in all cells, which is why some scientists think that only some cells, like brain cells, get sick and die in HD.

Targeting modifiers to control toxicity

In 2015, a large study was published by the Genetic Modifiers of Huntington’s Disease (GeM-HD) Consortium, a collective of scientists who pooled their ideas and resources to try and figure out why folks with the same CAG number might get symptoms of disease earlier or later in life. This study looked at the entire genetic makeup of over 4,000 people with HD. This study identified genes that can influence when symptoms of HD might begin. They dubbed the genes that alter age of onset “modifiers”, since they modify when someone will show signs of disease.

Lots of the modifier genes have links to how DNA is repaired and seem to influence expansion of the CAG repeatCAG repeat The stretch of DNA at the beginning of the HD gene, which contains the sequence CAG repeated many times, and is abnormally long in people who will develop HD in the HD gene. A key idea that arose from the GeM-HD team and subsequent studies is that people who have changes in these modifiers that scientists predict will slow somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain., seem to get HD later.

Some researchers think if we can control modifiers so that somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. is slowed, we could prevent the second step in the process of HD – toxicity and cell death. For this reason, a lot of scientists have been studying modifier genes that control somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain.. One such group is led by Jim Gusella, who was one of the key people on the 2015 GeM-HD paper.

A recently published study, driven by Zach McLean from Jim’s group details something quite curious. They noticed that drugs that can lower the levels of HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 also have off-target effects on modifiers that control somatic instabilitysomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain..

HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering drugs

“It turns out that branaplam and risdiplam both lower HTT and can also slow the rate of CAG expansion.”

The HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering drugs tested in this current study are branaplam and risdiplam. These drugs are small molecules that can be taken orally. Both are a type of drug called splice modulators – they work by introducing a stop sign in the middle of the HTT message. The cell reads this stop sign, sees that it’s out of place and doesn’t make sense, and doesn’t bother turning the message into protein.

Your eyes may have widened when you saw the name branaplam. This is the same drug that was tested in the failed Phase 2 VIBRANT-HD trial by Novartis. We previously wrote about the halting of this trial for safety reasons.

Risdiplam is an agency-approved medication used for the treatment of spinal muscular atrophy (SMA). For that disease, it works by increasing the amounts of a protein that people with SMA are missing. Risdiplam, sold as Evrysdi, was approved by the FDA in August of 2020 and the European Medicines Agency (EMA) in March of 2021. Risdiplam has been approved for SMA in over 80 countries.

Interestingly, risdiplam also lowers HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15. That means that people have safely been taking a HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering drug for several years. However, those people don’t have HD, which could make a difference.

Ability to target doesn’t equal specificity

One thing to note about some oral splice modulators that lower HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 is that they’re not specific. They’re not designed to only and specifically target HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15. They work by including bits of message, like stop signs, for many different genes. These off-target effects have caused scientists to suspect that they could have unintended consequences.

To better understand these unintended consequences, the team added branaplam and risdiplam to cells in a dish. What they found was quite serendipitous! It turns out that branaplam and risdiplam both lower HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 and can also slow the rate of CAG expansion. This is because these drugs also target a gene called PMS1. PMS1 just so happens to be one of those modifiers that was identified in the GeM-HD study. It’s thought that the less PMS1 people have, the later they start to show symptoms of HD.

In cells in a dish, branaplam and risdiplam seem to slow HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. by including a premature stop sign in the PMS1 message. Because of this, the cell lowers the amounts of PMS1 in the same way that it lowers HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15. With less PMS1, there is less CAG expansion in HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15. Quite fortuitous!

Not all HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-targeting splice modulators will work the same

The team behind this study note that there are differences between branaplam and risdiplam. While branaplam targets HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 more than PMS1, risdiplam does the opposite; risdiplam targets PMS1 more than HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15. Additionally, branaplam’s effects on somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. seem to only occur through PMS1, but risdiplam has effects on expansion outside of PMS1.

So while both drugs target HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 and PMS1, they each have unique effects. This means they could also be targeting other genes differently. Adding to this complexity, these drugs work by recognizing spelling in the genetic code. Since we all have little changes in our genetic spelling that make us unique, they may work differently in different people. This study highlights the caution that needs to be taken because of this.

Another similar drug that wasn’t tested in this study is PTC-518. This drug works in a very similar way and is currently being tested in a Phase 2 trial by PTC Therapeutics. We can’t infer anything about PTC-518 from this new work because it wasn’t included in the current study. So we don’t know exactly how similar or different it is from branaplam or risdiplam.

Is PMS1 the new target to beat?

This new study bolsters PMS1 as a potential target to go after to treat HD to reduce somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain.. However researchers need to be cautious when targeting genes that control somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain.. These genes also regulate how our DNA is repaired, which is critical for maintaining integrity of our genetic sequence and preventing cancer.

“You may be wondering if this new data means branaplam is coming back to clinical trials for HD. The short answer – no.”

Researchers also have to first work out how much to lower PMS1, or other genes that control somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain.. They need to find the sweet spot for lowering them enough to slow somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. and provide therapeutic benefit. This study only assessed PMS1 in cells in a dish. This would have to move to mouse models next.

Does this mean a resurgence for branaplam?

You may be wondering if this new data means branaplam is coming back to clinical trials for HD. The short answer – no. While there are no immediate plans to test branaplam in the clinic for HD, other splice modulators are moving forward. We can still learn quite a bit about HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15 lowering splice modulators that are moving forward by studying branaplam in the lab.

By studying branaplam and other drugs with similar mechanisms of action, we can get a better idea of how they’re similar and how they’re different. Knowing this, and studying which ones work better, can help identify other drugs with more specific effects on targets of choice. It can also help us understand how we can reduce unwanted side-effects.

So while this study identified a positive side-effect of a HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering splice modulator, that doesn’t mean it’s coming back to the clinic. However, knowing that HTTHTT one abbreviation for the gene that causes Huntington’s disease. The same gene is also called HD and IT-15-lowering drugs can also target somatic expansionsomatic expansion A process in which the CAG repeat in the Huntingtin gene can change over a person’s lifetime in some cells of the body, particularly in the brain. could inform ongoing and future trials using this class of drugs, perhaps leading to the development of drugs that target two birds with one stone.

Learn more

• Splice modulators target PMS1 to reduce somatic expansion of the Huntington’s disease-associated CAG repeat (open access)