Huntington’s ‘super assassin’ molecule could kill cancer

Table of Contents

  1. Faulty gene has too many repeated patterns
  2. Huntington’s produces ‘assassin molecule’

Scientists probing the reason why cancer is far less common in individuals with Huntington’s disease have revealed that the gene responsible for the fatal brain condition produces a molecule that is deadly to cancer cells.
cancer cell and dna strandWhy are people with Huntington’s disease less likely to be diagnosed with cancer?

In a recent paper published in the journal EMBO Reports, scientists from Northwestern University in Chicago, IL, note exactly how they tested the molecule in human and mouse cancer cells, as well as in mice with ovarian cancer.

“This molecule,” explains senior study author Marcus E. Peter, who’s a professor of cancer metabolism, “is a super assassin against all tumor cells. We’ve never seen anything this powerful.”

He and his colleagues hope that the discovery will lead to a short-lived treatment that can target and destroy cancer cells without triggering the progressive brain damage that occurs alongside Huntington’s disease.

Huntington’s disease is a fatal and inherited disorder that destroys nerve cells in the brain, causing a progressive decline in mental and physical ability. Symptoms will typically emerge between age 30 and 50 and progress over a period that lasts 10–25 years.

There are currently 30,000 people in the United States living with Huntington’s disease, as well as another 200,000 who are at risk of inheriting it.

Faulty gene has too many repeated patterns

There is currently no cure for Huntington’s disease, which arises from a fault in the huntingtin gene. The gene is passed from parent to child. Children with a parent who has the disease have a 50 percent chance of carrying the gene.

The faulty huntingtin gene contains more than a normal number of repeats of a certain sequence of nucleotides in its DNA code. Nucleotides are the “alphabet”of DNA and RNA and there are five of them: A, G, C, T, and U.

In Huntington’s disease, the huntingtin gene contains too many repeated sequences of CAG. The more repeated sequences of CAG in the gene, the earlier the disease develops.

The repeated sequences give rise to molecules called small interfering RNAs that attack genes that are important for cell survival, and they trigger a type of cell death that brain cells are susceptible to.

However, it seems that cancer cells are much more vulnerable to this type of cell death, which opens up the possibility of using the process to eliminate cancer cells in a way that does not damage healthy cells.

“We believe a short-term treatment cancer therapy for a few weeks might be possible, where we could treat a patient to kill the cancer cells without causing the neurological issues that Huntington’s patients suffer from.”

Prof. Marcus E. Peter

The cell death mechanism that is activated by small interfering RNAs was first identified in previous research
by Prof. Peter and first study author Dr. Andrea E Murmann, who is a research assistant professor in medicine.


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